{"id":174,"date":"2023-02-07T08:47:18","date_gmt":"2023-02-07T13:47:18","guid":{"rendered":"https:\/\/www.yorku.ca\/science\/research\/tbaumgardev\/?page_id=174"},"modified":"2026-03-12T16:21:09","modified_gmt":"2026-03-12T20:21:09","slug":"publications","status":"publish","type":"page","link":"https:\/\/www.yorku.ca\/science\/research\/tbaumgar\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\n<div style=\"height:24px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<script src=\"https:\/\/www.w3counter.com\/tracker.js?id=148599\"><\/script>\n\n\n\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-9d6595d7 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-vertically-aligned-center is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:100%\">\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-flow wp-block-group-is-layout-flow\">\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-9d6595d7 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-vertically-aligned-center is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:66.66%\">\n<blockquote class=\"wp-block-quote has-text-align-right is-layout-flow wp-block-quote-is-layout-flow\">\n<p><\/p>\n\n\n\n<p>Our book on&nbsp;<em><em>\u201cMain Group Strategies towards Functional Hybrid Materials\u201d&nbsp;<\/em><\/em><br>(Editors T. Baumgarter and F. J\u00e4kle; ISBN: 978-1-119-23597-2) <br>is now available&nbsp;<a href=\"https:\/\/www.wiley.com\/Main+Group+Strategies+towards+Functional+Hybrid+Materials-p-9781119235972\" target=\"_blank\" rel=\"noreferrer noopener\">here<\/a><\/p>\n\n\n\n<p><\/p>\n<\/blockquote>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:33.33%\">\n<figure class=\"wp-block-image\"><img loading=\"lazy\" decoding=\"async\" width=\"153\" height=\"233\" src=\"https:\/\/www.yorku.ca\/science\/research\/tbaumgar\/wp-content\/uploads\/sites\/750\/2023\/02\/image004_med_hr.jpeg\" alt=\"\" class=\"wp-image-708\"\/><\/figure>\n<\/div>\n<\/div>\n<\/div><\/div>\n<\/div>\n<\/div>\n\n\n\n<div style=\"height:32px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n<style>.kt-accordion-id174_4707a5-91 .kt-accordion-inner-wrap{column-gap:var(--global-kb-gap-md, 2rem);row-gap:8px;}.kt-accordion-id174_4707a5-91 .kt-accordion-panel-inner{padding-top:var(--global-kb-spacing-sm, 1.5rem);padding-right:var(--global-kb-spacing-sm, 1.5rem);padding-bottom:var(--global-kb-spacing-sm, 1.5rem);padding-left:var(--global-kb-spacing-sm, 1.5rem);}.kt-accordion-id174_4707a5-91 > .kt-accordion-inner-wrap > .wp-block-kadence-pane > .kt-accordion-header-wrap > .kt-blocks-accordion-header{padding-top:var(--global-kb-spacing-xxs, 0.5rem);padding-right:var(--global-kb-spacing-xs, 1rem);padding-bottom:var(--global-kb-spacing-xxs, 0.5rem);padding-left:var(--global-kb-spacing-xs, 1rem);}@media all and (max-width: 767px){.kt-accordion-id174_4707a5-91 .kt-accordion-inner-wrap{display:block;}.kt-accordion-id174_4707a5-91 .kt-accordion-inner-wrap .kt-accordion-pane:not(:first-child){margin-top:8px;}}<\/style>\n<div class=\"wp-block-kadence-accordion alignnone\"><div class=\"kt-accordion-wrap kt-accordion-id174_4707a5-91 kt-accordion-has-27-panes kt-active-pane-2 kt-accordion-block kt-pane-header-alignment-left kt-accodion-icon-style-arrow kt-accodion-icon-side-right\" style=\"max-width:none\"><div class=\"kt-accordion-inner-wrap\" data-allow-multiple-open=\"false\" data-start-open=\"2\">\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-3 kt-pane174_7abe4f-2d\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2026<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong><strong><strong>Non-Alternant-Hydrocarbon-Based Conjugated Phosphole Oxides<\/strong><\/strong><br><\/strong>S. Ambrico, A. Bhattacharjee, J. LeBlanc, K. Jaiswal, R. Dadgaryeganeh, E. Pradhan, T. Zeng, T. Baumgartner* \u00a0 \u00a0<br><em>Can J. Chem<\/em>.\u00a0<strong>2026<\/strong>,\u00a0<em>104<\/em>, 114-122. (<a href=\"https:\/\/doi.org\/10.1139\/cjc-2025-0079\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited article for special issue:\u00a0<em><a href=\"https:\/\/cdnsciencepub.com\/doi\/full\/10.1139\/cjc-2025-0211?af=R\" target=\"_blank\" rel=\"noreferrer noopener\">ISNA-20<\/a><\/em>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-27 kt-pane174_2d3ec3-3c\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2025<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong><strong><strong>From Aqua Green to Deep Red in One Step: Targeted Design of a Highly Luminescent Phosphacyclic Vat Orange 3 Dye<\/strong><\/strong><br><\/strong>R. Dadgaryeganeh, H. Le, S. Ambrico, A. Bhattacharjee, J. LeBlanc, A. Al Ramadhan, C. Romero-Nieto*, T. Baumgartner* &nbsp; &nbsp;<br><em>Org. Lett<\/em>.&nbsp;<strong>2025<\/strong>,&nbsp;<em>27<\/em>, 9705-9709. (<a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.5c02913\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited article for special issue on \u03c0-Conjugated Molecules and Materials)<\/p>\n\n\n\n<p><strong><strong><strong>From flat to twisted \u2013 multifunctional phosphacyclic nanocarbons based on Vat Orange 3<\/strong><\/strong><br><\/strong>R. Dadgaryeganeh, J. LeBlanc, E. Pradhan, D. Miao, A. Hussein, H. N. Hunter, T. Zeng*, C. Romero-Nieto*, T. Baumgartner* &nbsp; &nbsp;<br><em>Chem. Sci.<\/em>&nbsp;<strong>2025<\/strong>,&nbsp;<em>16<\/em>, 3680-3692. (<a href=\"https:\/\/doi.org\/10.1039\/D4SC07106A\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(2025 most popular nanoscience articles <a href=\"https:\/\/pubs.rsc.org\/en\/journals\/articlecollectionlanding?themeID=7ff1bc7a-0fe1-45a1-b617-515297fdbaa6\" target=\"_blank\" rel=\"noreferrer noopener\">collection<\/a>)<\/p>\n\n\n\n<p><strong><strong><strong>Self-assembly of Phosphole-lipids in 2D Films: The Influence of \u03c0-Interactions and Steric Constraints<\/strong><\/strong><br><\/strong>Z. Alinia, D. Miao, T. Baumgartner, C. E. DeWolf* &nbsp; &nbsp;<br><em>RSC Appl. Interfaces<\/em>&nbsp;<strong>2025<\/strong>,&nbsp;<em>2<\/em>, 460-471. (<a href=\"https:\/\/doi.org\/10.1039\/D4LF00361F\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-26 kt-pane174_69e743-18\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2024<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong><strong><strong>Tuning Electrostatics to Promote Ordered Monolayers of Phosphole-Lipids<\/strong><\/strong><br><\/strong>Z. Alinia, D. Miao, T. Baumgartner, C. E. DeWolf* &nbsp; &nbsp;<br><em>Langmuir<\/em>&nbsp;<strong>2024<\/strong>,&nbsp;<em>40<\/em>, 22301-22313. (<a href=\"https:\/\/doi.org\/10.1021\/acs.langmuir.4c02962\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong><strong><strong>Viologen-based solution-processable ionic porous polymers for electrochromic applications<\/strong><\/strong><br><\/strong>H. Miao, L. Chen, F. Xing, H. Li, T. Baumgartner*, X. He* &nbsp; &nbsp;<br><em>Chem<\/em>. <em>Sci.<\/em>&nbsp;<strong>2024<\/strong>,&nbsp;<em>15<\/em>, 7576-7585. (<a href=\"https:\/\/doi.org\/10.1039\/D4SC01408A\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong><strong><strong>Multivalency unlocked: The unique redox traits of the&nbsp;\u201ftripak\u2019\u2019 system<\/strong><\/strong><br><\/strong>N. Asok, T. Baumgartner* &nbsp; &nbsp;<br><em>Chem<\/em>&nbsp;<strong>2024<\/strong>,&nbsp;<em>10<\/em>, 756-758. (<a href=\"https:\/\/doi.org\/10.1016\/j.chempr.2024.02.009\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited Preview article)<\/p>\n\n\n\n<p><strong><strong>Modified Viologen- and Carbonylpyridinium-based Electrodes for Organic Batteries<\/strong><br><\/strong>X. He*, L. Chen, T. Baumgartner* &nbsp; &nbsp;<br><em>ACS Appl. Mater. Interfaces<\/em>&nbsp;<strong>2024<\/strong>,&nbsp;<em>16<\/em>, 48689-48705. (<a href=\"https:\/\/doi.org\/10.1021\/acsami.3c09856\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited Spotlight article for Forum on 'Organic Battery Materials')<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-25 kt-pane174_24005b-8b\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2023<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong><strong><strong>Rethinking the Lewis Acidity of Cationic Gallium and Indium Catalysts<\/strong><\/strong><br><\/strong>C. Goonesinghe, H.-J. Jung, I. O. Betinol, J. R. Gaffen, C. N. Garrard, J. Chang, K. Hosseini, H. Roshandel, K. Nyamayaro, B. Patrick, M. Ezhova, C. B. Caputo, T. Baumgartner, J. P. Reid, P. Mehrkhodavandi* &nbsp; &nbsp;<br><em>ACS Catal.<\/em>&nbsp;<strong>2023<\/strong>,&nbsp;<em>13<\/em>, 16148-16157. (<a href=\"https:\/\/doi.org\/10.1021\/acscatal.3c04918\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong><strong>Development of the P-Arylation of Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phosphole with Aryl Iodonium Salts<\/strong><br><\/strong>A. Hussein, N. Asok, V. A. B\u00e9land, J. R. Gaffen, J. LeBlanc, T. Baumgartner* &nbsp; &nbsp;<br><em>ChemPlusChem<\/em>&nbsp;<strong>2023<\/strong>,&nbsp;e202300133. (<a href=\"https:\/\/doi.org\/10.1002\/cplu.202300133\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited article for special collection 'Pnictogen Chemistry')<\/p>\n\n\n\n<p><strong><strong>Not So Innocent After All: Interfacial Chemistry Determines Charge-Transport Efficiency in Single-Molecule Junctions<\/strong><br><\/strong>A. Daaoub,  J. M. F. Morris,  V. A. B\u00e9land, P. Demay-Drouhard, A. Hussein, S. J. Higgins, H. Sadeghi, R. J. Nichols, A. Vezzoli*, T. Baumgartner*, S. Sangtarash* &nbsp; &nbsp;<br><em>Angew. Chem. Int. Ed.<\/em>&nbsp;<strong>2023<\/strong>,&nbsp;<em><em>62<\/em><\/em>,&nbsp;e202302150. (<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202302150\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong><strong>Exploring the Lewis Acidity and Reactivity of Neutral Pentacoordinate Dithienophospholes<\/strong><br><\/strong>N. Asok, B. A. Zondag, E. Pradhan, M. Odagwe, J. LeBlanc, J. C. Walsh, G. J. Bodwell, T. Zeng*, T. Baumgartner* &nbsp; &nbsp;<br><em>Chem. Eur. J.<\/em>&nbsp;<strong>2023<\/strong>,&nbsp;<em>29<\/em>, e202300173. (<a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/chem.202300173\" target=\"_blank\" rel=\"noreferrer noopener\">link)<\/a><br>(invited article for special collection 'ISNA-19')<\/p>\n\n\n\n<p><strong>Unique Phosphorus-Based Avenues for the Tuning of Functional&nbsp;Materials<br><\/strong>N. Asok, J. R. Gaffen, T. Baumgartner* &nbsp; &nbsp;<br><em>Acc. Chem. Res.<\/em>&nbsp;<strong>2023<\/strong>,&nbsp;<em>56<\/em>,&nbsp;536-547. (<a href=\"https:\/\/doi.org\/10.1021\/acs.accounts.2c00707\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited account article, 'most read\u2019&nbsp;in 03\/2023)<\/p>\n\n\n\n<p><strong>Probing the Impact of Solvent on the Strength of Lewis Acids via Fluorescent Lewis Adducts<\/strong><br>A. E. Laturski, J. R. Gaffen, P. Demay-Drouhard, C. B. Caputo*, T. Baumgartner*<br><em>Precis. Chem.&nbsp;<\/em><strong>2023<\/strong>,&nbsp;<em>1<\/em>, 49-56. (<a href=\"https:\/\/doi.org\/10.1021\/prechem.2c00009\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited article for new journal launch, 'most read\u2019&nbsp;in 2023)<\/p>\n\n\n\n<p><strong>Fluorescence-based Measurement of the Lewis Acidities of Lanthanide Triflates in Solution<br><\/strong>P. Demay-Drouhard,&nbsp;J. R. Gaffen, C. B. Caputo*,&nbsp;T. Baumgartner*<br><em>Can. J. Chem.&nbsp;<\/em><strong>2023<\/strong>,<em>&nbsp;101<\/em>,&nbsp;146-153.&nbsp;(<a href=\"https:\/\/doi.org\/10.1139\/cjc-2022-0115\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited article for special issue:&nbsp;<em>Celebrating the Life of Suning Wang<\/em>; <span style=\"text-decoration: underline;\">Editor's Choice<\/span>)<br>ChemRxiv:&nbsp;<a href=\"https:\/\/doi.org\/10.26434\/chemrxiv-2022-zprf5\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.26434\/chemrxiv-2022-zprf5<\/a><\/p>\n\n\n\n<p><strong>Cost-Effective Vat Orange 3-Derived Organic Cathodes for Electrochemical Energy Storage<br><\/strong>L. Chen,&nbsp;F. Xing,&nbsp;Q. Lin,&nbsp;A. Waqas, X. Wang, T. Baumgartner*, X. He*<br><em>Batteries &amp; Supercaps<\/em>&nbsp;<strong>2023<\/strong>,&nbsp;<em>5<\/em>, e202200406.&nbsp;(<a href=\"https:\/\/doi.org\/10.1002\/batt.202200406\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited article for special collection on organic batteries,&nbsp;<a href=\"https:\/\/doi.org\/10.1002\/batt.202300016\" target=\"_blank\" rel=\"noreferrer noopener\">cover feature<\/a>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-4 kt-pane174_3e694d-a2\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2022<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Rational Design of Bio-Derived Four-Electron-Accepting Carbonyl-N-methylpyridinium Species for High-Performance Lithium\/Organic Batteries<br><\/strong>X. Wang, W. Xue, G. Guo, L. Chen, T. Baumgartner, X. He*<br><em>Cell Rep. Phys. Sci.<\/em>&nbsp;<strong>2022<\/strong>,<em>&nbsp;3<\/em>, 100951(<a href=\"https:\/\/doi.org\/10.1016\/j.xcrp.2022.100951\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>ChemRxiv:&nbsp;<a href=\"https:\/\/doi.org\/10.26434\/chemrxiv-2021-cf3mz\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.26434\/chemrxiv-2021-cf3m<\/a><\/p>\n\n\n\n<p><strong>Tailored Solvatochromic NIR Phosphorus-Chromophores via Selective P\u2212N and P\u2212C Chemistry in P-Heteropines<br><\/strong>Z. Yang,&nbsp;X. Li,&nbsp;K. Yang,&nbsp;Z. Zhang,&nbsp;Y. Wang,&nbsp;N. Yu,&nbsp;T. Baumgartner,&nbsp;Y. Ren*<br><em>Org. Lett.&nbsp;<\/em><strong>2022<\/strong>,&nbsp;<em>24<\/em>, 2045-2049 (<a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.2c00570\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-5 kt-pane174_de9004-db\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2021<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Conjugated Polymers with Benzoyl-N-methylpyridinium units: An Effective Design Strategy for High-Performance Lithium-Ion Batteries<\/strong><br>G. Guo,&nbsp;X. Wang, L. Chen, T. Baumgartner, X. He*<br><em>Chem. Mater.&nbsp;<\/em><strong>2021<\/strong>,&nbsp;<em>33<\/em>, 4596-4605 (<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.chemmater.1c01072\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Donor\u2013acceptor\u2013acceptor-type near-infrared fluorophores that contain dithienophosphole oxide and boryl groups: Effect of the boryl group on the nonradiative decay<\/strong><br>Y. Sugihara, N. Inai, M. Taki, T. Baumgartner, R. Kawakami, T. Saitou, T. Imamura, T. Yanai*, S. Yamaguchi*<br><em>Chem. Sci.&nbsp;<\/em><strong>2021<\/strong>,&nbsp;<em>12<\/em>, 6333-6341.&nbsp;(<a href=\"https:\/\/doi.org\/10.1039\/D1SC00827G\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(Hot Article Collection)<\/p>\n\n\n\n<p><strong>Structure-reactivity studies on hypervalent square-pyramidal dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phospholes&nbsp; &nbsp;&nbsp;<\/strong><br>N. Asok, J. R. Gaffen, E. Pradhan, T. Zeng*, T. Baumgartner* &nbsp; &nbsp;<br><em>Dalton Trans.<\/em>&nbsp;<strong>2021<\/strong>,&nbsp;<em>50<\/em>,&nbsp;2243-2252. (<a href=\"https:\/\/doi.org\/10.1039\/D1DT00062D\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>YorkSpace:&nbsp;<a href=\"http:\/\/hdl.handle.net\/10315\/40815\">http:\/\/hdl.handle.net\/10315\/40815<\/a><\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-6 kt-pane174_614c4e-7b\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2020<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Fluorescent Lewis Adducts: A Practical Guide to Relative Lewis Acidity<\/strong><br>J. N. Bentley, S. A. Elgadi, J. R. Gaffen, P. Demay-Drouhard, T. Baumgartner*, C. B. Caputo*<br><em>Organometallics<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>39<\/em>,&nbsp;3645-3655. (<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.organomet.0c00389\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>('most read\u2019&nbsp;in 10\/2020 and 11\/2020)<br>ChemRxiv:&nbsp;<a href=\"https:\/\/chemrxiv.org\/articles\/preprint\/Fluorescent_Lewis_Adducts_A_Refined_Guide_for_Lewis_Acidity\/10292957\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.26434\/chemrxiv.10292957.v2<\/a><\/p>\n\n\n\n<p><strong>Highly Luminescent 4-Pyridyl-Extended Dithieno[3,2-<em>b<\/em>:2\u2032,3\u2032-<em>d<\/em>]phospholes<br><\/strong>P. Demay-Drouhard, T. Baumgartner*<br><em>J. Org. Chem.<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>85<\/em>,&nbsp;14627-14633<em>.<\/em>&nbsp;(<a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.joc.0c01369\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited article for special issue:&nbsp;<em>The New Golden Age of Organophosphorus Chemistry<\/em>)<br>ChemRxiv:&nbsp;<a href=\"https:\/\/chemrxiv.org\/articles\/preprint\/Highly_Luminescent_4-Pyridyl-Extended_Dithieno_3_2-b_2_3_-d_phospholes\/12455357\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.26434\/chemrxiv.12455357.v1<\/a><\/p>\n\n\n\n<p><strong>Phosphoryl- and Phosphonium-Bridged Viologens as Stable Two- and Three-Electron Acceptors for Organic Electrodes<br><\/strong>C. R. Bridges, A. M. Borys, V. A. B\u00e9land, J. R. Gaffen, T. Baumgartner*<br><em>Chem. Sci.&nbsp;<\/em><strong>2020<\/strong>,&nbsp;<em>11<\/em>, 10483-10487<em>.&nbsp;<\/em>(<a href=\"https:\/\/doi.org\/10.1039\/D0SC04183A\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>ChemRxiv:&nbsp;<a href=\"https:\/\/chemrxiv.org\/articles\/preprint\/Phosphoryl-_and_Phosphonium-Bridged_Viologens_as_Stable_Two-_and_Three-Electron_Acceptors_for_Organic_Electrodes\/12711770\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.26434\/chemrxiv.12711770.v1<\/a><\/p>\n\n\n\n<p><strong>Lewis Acids and Bases as Molecular Dopants for Organic Semiconductors<br><\/strong>C. R. Bridges*, T. Baumgartner*<br><em>J. Phys. Org. Chem.&nbsp;<\/em><strong>2020<\/strong>,&nbsp;<em>33<\/em>, e4077. (<a href=\"https:\/\/doi.org\/10.1002\/poc.4077\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited review,&nbsp;<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/poc.4124\" target=\"_blank\" rel=\"noreferrer noopener\">cover page<\/a>)<br>YorkSpace:&nbsp;<a href=\"http:\/\/hdl.handle.net\/10315\/38844\">http:\/\/hdl.handle.net\/10315\/38844<\/a><\/p>\n\n\n\n<p><strong>Phosphaviologen-based Pyrene-Carbon Nanotube Composites for Stable Battery Electrodes&nbsp;<\/strong><br>C. R. Bridges, M. Stolar, T. Baumgartner*<br><em>Batteries &amp; Supercaps<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>3<\/em>, 268-274.&nbsp;(<a href=\"https:\/\/doi.org\/10.1002\/batt.201900164\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/epdf\/10.1002\/batt.202000031\" target=\"_blank\" rel=\"noreferrer noopener\">cover page<\/a>); highlighted on&nbsp;BBC World Service Radio, &nbsp;<a href=\"https:\/\/www.inverse.com\/innovation\/batteries\" target=\"_blank\" rel=\"noreferrer noopener\">inverse.com<\/a>,&nbsp;<a href=\"https:\/\/www.advancedsciencenews.com\/one-step-closer-to-organic-batteries\/\" target=\"_blank\" rel=\"noreferrer noopener\">Advanced Science News<\/a>,&nbsp;<a href=\"https:\/\/www.electronicsweekly.com\/news\/research-news\/cheap-abundant-materials-replace-electrodes-lithium-battery-2020-03\/\" target=\"_blank\" rel=\"noreferrer noopener\">ElectronicsWeekly.com<\/a><br>YorkSpace:&nbsp;<a href=\"http:\/\/hdl.handle.net\/10315\/38130\">http:\/\/hdl.handle.net\/10315\/38130<\/a><\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-7 kt-pane174_f19004-ef\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2019<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Poly(5-vinylbenzothiadiazole) for High-Performance Lithium-Ion Batteries<\/strong>&nbsp;<br>L. Chen, C. R. Bridges, G. Gao, T. Baumgartner*, X. He*<br><em>ACS Appl. Energy Mater.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>2<\/em>, 7315-7320.&nbsp;(<a href=\"https:\/\/doi.org\/10.1021\/acsaem.9b01285\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>YorkSpace:&nbsp;<a href=\"http:\/\/hdl.handle.net\/10315\/38131\">http:\/\/hdl.handle.net\/10315\/38131<\/a><\/p>\n\n\n\n<p><strong>A Simple and Effective Method of Determining Lewis Acidity by Using Fluorescence&nbsp;<\/strong><br>J. R. Gaffen, J. N. Bentley, L. C. Torres, C. Chu, T. Baumgartner,* C. B. Caputo*<br><em>Chem&nbsp;<\/em><strong>2019<\/strong>,&nbsp;<em>5<\/em>, 1567-1583. (<a href=\"https:\/\/doi.org\/10.1016\/j.chempr.2019.03.022\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Using boron to tune the geometry of a non-fullerene acceptor for improved organic solar cell performance&nbsp;<\/strong><br>T. A. Welsh, A. Laventure, A. F. Alahmadi, G. Zhang, T. Baumgartner, Y. Zou, F. J\u00e4kle,* G. C. Welch*<br><em>ACS Appl. Energy Mater.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>2<\/em>, 1229-1240.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1021\/acsaem.8b01793\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Synthesis a Trivalent&nbsp;<em>P<\/em>-Chloro-Dithienophosphole&nbsp;and Its Reactivity of&nbsp;with Organometallic Reagents<\/strong><br>J. R. Gaffen, Z. Wang, T. Baumgartner*<br><em>Eur. J. Inorg. Chem.&nbsp;<\/em><strong>2019<\/strong>, 1612-1620. (<a href=\"https:\/\/doi.org\/10.1002\/ejic.201801229\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited article for special issue honouring Koop Lammertsma and Edgar Niecke)<br>YorkSpace:&nbsp;<a href=\"http:\/\/hdl.handle.net\/10315\/37637\">http:\/\/hdl.handle.net\/10315\/37637<\/a><\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-8 kt-pane174_6f3881-f4\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2018<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>A Highly Stable Organic Radical Cation<\/strong>&nbsp;<br>M. Berville, J. Richard, M. Stolar, S. Choua, N. Le Breton, C. Gourlaouen, C. Boudon, L. Ruhlmann, T. Baumgartner, J. A. Wytko,* J. Weiss*<br><em>Org. Lett.&nbsp;<\/em><strong>2018<\/strong>,&nbsp;<em>20<\/em>,&nbsp;8004-8008.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.8b03579\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)&nbsp;<\/p>\n\n\n\n<p><strong>An Unexpected \u2018Step-Conjugated\u2019 Biphosphole via Unique P-P Bond Formation<\/strong><br>Z. Wang, N. Asok, J. Gaffen, Y. Gottlieb, W. Bi, C.&nbsp;Gendy, R. Dobrovetsky,* T. Baumgartner*<br><em>Chem&nbsp;<\/em><strong>2018<\/strong>,&nbsp;<em>4<\/em>, 2628-2643. (<a href=\"https:\/\/www.cell.com\/chem\/fulltext\/S2451-9294(18)30374-7\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)&nbsp; &nbsp; &nbsp; &nbsp;<br>(for a&nbsp;\u2018preview\u2019, see&nbsp;<a href=\"https:\/\/www.cell.com\/chem\/fulltext\/S2451-9294(18)30493-5\" target=\"_blank\" rel=\"noreferrer noopener\">here<\/a>)<\/p>\n\n\n\n<p><strong>Functional Conjugated Pyridines via Main-Group Element Tuning<\/strong><br>M. Stolar, T. Baumgartner*<br><em>Chem. Commun.<\/em>&nbsp;<strong>2018<\/strong>,&nbsp;<em>54<\/em>, 3311-3322. (<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2018\/CC\/C8CC00373D#!divAbstract\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<a href=\"http:\/\/www.nrcresearchpress.com\/doi\/full\/10.1139\/cjc-2017-0619#.WrOivGa-LjA\" target=\"_blank\" rel=\"noreferrer noopener\"><br><\/a>(invited Feature article)<\/p>\n\n\n\n<p><strong>On the Reactivity of P-Chloro Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phosphole Oxide<\/strong><br>Z. Wang, D. Spasyuk, T. Baumgartner*<br><em>Can. J. Chem.<\/em>&nbsp;<strong>2018<\/strong>,&nbsp;<em>&nbsp;96,&nbsp;<\/em>555-560. (<a href=\"http:\/\/www.nrcresearchpress.com\/doi\/full\/10.1139\/cjc-2017-0619#.WrOivGa-LjA\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited article for special issue honouring Neil Burford)<\/p>\n\n\n\n<p><strong>Dithienophosphole-based molecular electron acceptors constructed using direct (hetero)arylation cross-coupling methods<\/strong><br>T. A. Welsh, A. Laventure, T. Baumgartner, G. C. Welch*<br><em>J. Mater. Chem. C&nbsp;<\/em><strong>2018<\/strong>,&nbsp;<em>&nbsp;6<\/em>, 2148-2154. (<a href=\"http:\/\/dx.doi.org\/10.1039\/C7TC05631A\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Exploration of Hypervalent Lewis Acid\/Base Interactions in 2-(2\u2019-Thiazolyl)-3-thienylphosphanes<\/strong><br>N. Grenon, T. Baumgartner*&nbsp;<br><em>Inorg. Chem.&nbsp;<\/em><strong>2018<\/strong>,&nbsp;<em>57<\/em>, 1630-1644. (<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.inorgchem.7b03008\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-9 kt-pane174_cfd816-54\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2017<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Electron-Accepting&nbsp;<em>pi<\/em>-Conjugated Species with 1,8-Naphthalic Anhydride or Diketophosphanyl Units<\/strong><br>S. S\u00e1nchez, A. Y. Y. Woo, T. Baumgartner*&nbsp;<br><em>Mater. Chem. Front.&nbsp;<\/em><strong>2017<\/strong>,&nbsp;<em>1<\/em>, 2324-2334. (<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2017\/qm\/c7qm00336f#!divAbstract\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Viologens and their Application as Functional Materials<\/strong><br>L. Striepe, T. Baumgartner*<br><em>Chem. Eur. J.&nbsp;<\/em><strong>2017<\/strong>,&nbsp;<em>23<\/em>, 16924-16940. (<a href=\"http:\/\/dx.doi.org\/10.1002\/chem.201703348\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(\u2018most accessed\u2019 in 11\/2017-10\/2018, 'most cited\u2019 in 2019)<\/p>\n\n\n\n<p><strong>Water-Soluble Phosphaviologens for Effective Photoinduced Charge&nbsp;Separation<\/strong><br>M. Stolar, B. Heyne, T. Baumgartner*<br><em>Organometallics<\/em>&nbsp;<strong>2017<\/strong>,&nbsp;<em>36<\/em>, 2685-2691. (<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.organomet.7b00313\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a><a href=\"http:\/\/dx.doi.org\/10.1039\/C6QO00872K\" target=\"_blank\" rel=\"noreferrer noopener\">)<\/a><br>(invited article for themed issue:&nbsp;<em>Tailoring the Optoelectronic Properties of Organometallic Compounds&nbsp;with&nbsp;Main Group Elements<\/em>)<\/p>\n\n\n\n<p><strong>Synthesis and properties of electron accepting star-shaped phosphaviologen oligomers<\/strong><br>L. Striepe,&nbsp;M. Vespa, T. Baumgartner*<br><em>Org. Chem. Front.<\/em>&nbsp;<strong>2017<\/strong>,&nbsp;<em>4<\/em>, 717-723. (<a href=\"http:\/\/dx.doi.org\/10.1039\/C6QO00872K\" target=\"_blank\" rel=\"noreferrer noopener\">link)<\/a><br>(invited article for themed issue:&nbsp;<em>Novel \u03c0-electron molecular scaffolds<\/em>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-10 kt-pane174_a99bd9-34\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2016<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Cooperative-Assembly of Phosphole-Lipids and Single-Walled Carbon Nanotubes<\/strong><br>Y. Ren,&nbsp;J. Gao,&nbsp;A. K. Hailey,&nbsp;T. Baumgartner,&nbsp;Y.-L. Loo*<br><em>Chem. Mater.&nbsp;<\/em><strong>2016<\/strong>,&nbsp;<em>28<\/em>, 8407-8414. (<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.chemmater.6b03987\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Xylene-Bridged Phosphaviologen Oligomers and Polymers as High-Performance Electrode Modifiers for&nbsp;Li-Ion&nbsp;Batteries<\/strong><br>M. Stolar,&nbsp;C. Reus, T. Baumgartner*<br><em>Adv. Energy Mater.&nbsp;<\/em><strong>2016<\/strong>,&nbsp;<em>6<\/em>,&nbsp;1600944. (<a href=\"http:\/\/dx.doi.org\/10.1002\/aenm.201600944\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Dithienophosphole-based Phosphinamides with Intriguing Self-Assembly Behavior<\/strong><br>Z. Wang,&nbsp;B. S. Gelfand, T. Baumgartner*<br><em>Angew. Chem.<\/em><strong>&nbsp;2016<\/strong>,&nbsp;<em>128<\/em>,&nbsp;3542-3546;&nbsp;<em>&nbsp;Angew. Chem. Int. Ed.&nbsp;<\/em><strong>2016<\/strong>,&nbsp;<em>55<\/em>, 3481-3485. (<a href=\"http:\/\/dx.doi.org\/10.1002\/anie.201511171\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Tuning the Aggregation-Induced Emission Behavior and Self-Assembly of Phosphole-Lipids<\/strong><br>Z. Wang,&nbsp;B. S. Gelfand, P. Dong, S. Trudel, T. Baumgartner*<br><em>J. Mater. Chem. C&nbsp;<\/em><strong>2016<\/strong>,&nbsp;<em>4<\/em>, 2936-2944. (<a href=\"http:\/\/dx.doi.org\/10.1039\/C5TC03311J\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited article for themed issue:&nbsp;<em>&nbsp;Shape-Responsive Fluorophores<\/em>)<\/p>\n\n\n\n<p><strong>A Structure-Property ¿ì²¥ÊÓƵ Toward&nbsp;<em>pi<\/em>-Extended Phosphole Chromophores with Ambipolar Redox Properties<\/strong><br>Y. Ren, T. Baumgartner*<br><em>Can. J. Chem.&nbsp;<\/em><strong>2016<\/strong>,&nbsp;<em>94<\/em>, 297-304. (<a href=\"http:\/\/www.nrcresearchpress.com\/doi\/full\/10.1139\/cjc-2015-0347#.VfwghbTwE0q\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(<em>University of Calgary 50th&nbsp;anniversary issue<\/em>)<\/p>\n\n\n\n<p><strong>Stimuli-Responsive Chromism in Organophosphorus Chemistry<\/strong><br>C. Reus, T. Baumgartner*<br><em>Dalton Trans.&nbsp;<\/em><strong>2016<\/strong>,&nbsp;<em>45<\/em>, 1850-1855. (<a href=\"http:\/\/dx.doi.org\/10.1039\/C5DT02758F\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited Frontier article for themed issue:&nbsp;<em>Phosphorus Chemistry: Discoveries and Advances<\/em>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-11 kt-pane174_dacfff-c2\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2015<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Structure-Property Studies of&nbsp;<em>P<\/em>-Triarylamine-Substituted Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phospholes<\/strong><br>H.&nbsp;Puntscher, P. Kautny, B. St\u00f6ger, A. Tissot, C. Hametner, H. R. Hagemann, J. Fr\u00f6hlich, T. Baumgartner,*&nbsp;D. Lumpi*<br><em>RSC Adv.<\/em>&nbsp;<strong>2015<\/strong>,&nbsp;<em>5<\/em>,&nbsp;93797-93807.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1039\/C5RA13651B\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>A Convenient N-Arylation Route for Electron-Deficient Pyridines: The Case of&nbsp;<em>pi<\/em>-Extended Electrochromic&nbsp;Phosphaviologens<\/strong><br>C. Reus,&nbsp;M. Stolar, J. Vanderkley, J. Nebauer, T. Baumgartner*<br><em>J. Am. Chem. Soc.&nbsp;<\/em><strong>2015<\/strong>,&nbsp;<em>137<\/em>, 11710-11717. (<a href=\"http:\/\/dx.doi.org\/10.1021\/jacs.5b06413\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Synthesis and Tunability of Highly Electron-Accepting, N-Benzylated \u2018Phosphaviologens\u2019<\/strong><br>M. Stolar, J. Borau-Garcia, M. Toonen, T. Baumgartner*<br><em>J. Am. Chem. Soc.&nbsp;<\/em><strong>2015<\/strong>,&nbsp;<em>137<\/em>,&nbsp;3366-3371. (<a href=\"http:\/\/dx.doi.org\/10.1021\/ja513258j\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(Highlighted in SYNFACTS 05\/2015)<\/p>\n\n\n\n<p><strong>P-Containing Heteroarenes: Synthesis, Properties, Applications<\/strong><br>M. Stolar, T. Baumgartner*&nbsp;<br>in:&nbsp;<em>Polycyclic Arenes and Heteroarenes: Synthesis, Properties, and Applications<\/em>, Wiley-VCH,&nbsp;<strong>2015<\/strong>,&nbsp;<em>309-329<\/em>. (<a href=\"http:\/\/ca.wiley.com\/WileyCDA\/WileyTitle\/productCd-3527338470.html\">link<\/a>)<br>(invited book chapter)<\/p>\n\n\n\n<p><strong>Organophosphorus Avenues Toward Self-Assembled Conjugated Soft Materials<\/strong>&nbsp;<br>Z. Wang, T. Baumgartner*&nbsp;<br><em>Chem. Rec.<\/em>&nbsp;<strong>2015<\/strong>,&nbsp;<em>15<\/em>, 199-217.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1002\/tcr.201402061\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)&nbsp;<br>(invited personal account article for special issue on Novel Aromatics - Nozoe\/ISNA)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-12 kt-pane174_013744-de\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2014<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Insights on the Design and Electron-Acceptor Properties of Conjugated Organophosphorus Materials<\/strong>&nbsp;<br>T. Baumgartner&nbsp;<br><em>Acc. Chem. Res.<\/em>&nbsp;<strong>2014<\/strong>,&nbsp;<em>47<\/em>, 1613-1622. (<a href=\"http:\/\/dx.doi.org\/10.1021\/ar500084b\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)&nbsp;<br>(invited account article)<\/p>\n\n\n\n<p><strong>Synthesis and Properties of Cholesteric Click-Phospholes<\/strong><br>X.-M. He, J.-B. Lin, W. H. Kan, S. Trudel, T. Baumgartner*<br><em>Org. Lett.<\/em>&nbsp;<strong>2014<\/strong>,&nbsp;<em>16<\/em>, 1366-1369.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1021\/ol500129p\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Phosphorus-Containing Materials for Organic Electronics<\/strong><br>M. Stolar, T. Baumgartner*&nbsp;<br><em>Chem. Asian J.<\/em>&nbsp;<strong>2014<\/strong>,&nbsp;<em>9<\/em>,&nbsp;1212-1225.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1002\/asia.201301670\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited focus review &amp; featured article, most cited list)<\/p>\n\n\n\n<p><strong>P-Terthienyl Functionalized Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phospholes<\/strong>&nbsp; &nbsp;&nbsp;<br>C. J. Chua, Y. Ren, M. Stolar, S. Xing, T. Linder, T. Baumgartner*<br><em>Eur. J. Inorg. Chem.&nbsp;<\/em><strong>2014<\/strong>, 1767-1774.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1002\/ejic.201301065\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited contribution for cluster issue on<em>&nbsp;Advances in Phosphorus Chemistry<\/em>)<\/p>\n\n\n\n<p><strong>Molecular Engineering of \u201cClick\u201d-Phospholes Towards Self-Assembled Luminescent Soft Materials<\/strong><br>X.-M. He, J.-B. Lin, W. H. Kan, P. Dong, S. Trudel, T. Baumgartner*&nbsp;<br><em>Adv. Funct. Mater.&nbsp;<\/em><strong>2014<\/strong>,<em>&nbsp;24<\/em>, 897-906.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1002\/adfm.201302294\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adfm.201470039\/abstract\" target=\"_blank\" rel=\"noreferrer noopener\">front cover page<\/a>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-13 kt-pane174_5a36bf-bb\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2013<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Synthesis and Properties of a Dicationic&nbsp;<em>pi<\/em>-Extended Dithieno[3,2-<em>c<\/em>:2\u2019,3\u2019-<em>e<\/em>]-2,7-diketophosphepin<\/strong>&nbsp;<br>X.-M. He, T. Baumgartner*&nbsp;<br><em>Organometallics&nbsp;<\/em><strong>2013<\/strong>,&nbsp;<em>32<\/em>, 7625-7628. (<a href=\"http:\/\/dx.doi.org\/10.1021\/om400991a\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Synthesis of P-Triazole Dithienophospholes and a Cyclodextrin-based Sensor via Click Chemistry<\/strong><br>X.-M. He, P. Zhang, J.-B. Lin, H. V. Huynh, S. E. Navarro Mu\u00f1oz, C.-C. Ling, T. Baumgartner*&nbsp;&nbsp;<br><em>Org. Lett.<\/em>&nbsp;<strong>2013<\/strong>,&nbsp;<em>15<\/em>, 5322-5325.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1021\/ol402582p\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Phosphinine-Lipids: A Successful Marriage between Electron-Acceptor and Self-Assembly Features<\/strong><br>X.-M. He, J.-B. Lin, W. H. Kan, T. Baumgartner*<br><em>Angew. Chem.<\/em><strong>&nbsp;2013<\/strong>,&nbsp;<em>125<\/em>,&nbsp;9160-9164;&nbsp;<em>Angew. Chem. Int. Ed.<\/em>&nbsp;<strong>2013<\/strong>,&nbsp;<em>52<\/em>, 8990-8994.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1002\/anie.201303729\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Luminescent P-Benzyl Dithienophospholes - A Joint Experimental and Theoretical Investigation<\/strong><br>Z. Wang, A. Y. Y. Woo, T. Baumgartner*<br><em>Aust. J. Chem.<\/em>&nbsp;<strong>2013<\/strong>,&nbsp;<em>66<\/em>, 1171-1178.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1071\/CH13220\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited contribution for 'research front' issue on&nbsp;<em>main group chemistry<\/em>)<\/p>\n\n\n\n<p><strong>Organic&nbsp;<em>n<\/em>-Type Materials for Charge Transport and Charge Storage Applications<\/strong><br>M. Stolar, T. Baumgartner*<br><em>Phys. Chem. Chem. Phys.<\/em>&nbsp;<strong>2013<\/strong>,&nbsp;<em>15<\/em>, 9007-9024.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1039\/C3CP51379C\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited perspective, \u2018most accessed' in 05-06\/2013)<\/p>\n\n\n\n<p><strong>Halochromic Generation of White Light Emission Using a Single Dithienophosphole Luminophore<\/strong><br>H. V. Huynh, X.-M. He, T. Baumgartner*<br><em>Chem. Commun.&nbsp;<\/em><strong>2013<\/strong>,&nbsp;<em>49<\/em>, 4899-4901. (<a href=\"http:\/\/dx.doi.org\/10.1039\/C3CC41510D\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(highlighted under \"<a href=\"http:\/\/www.acs.org\/content\/acs\/en\/noteworthy-chemistry\/archive\/june-24.html#link6\">Noteworthy Chemistry<\/a>\" on ACS website)<\/p>\n\n\n\n<p><strong>Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phospholes: A Look Back at the First Decade<\/strong><br>C. Romero-Nieto,* T. Baumgartner*<br><em>SYNLETT<\/em>&nbsp;<strong>2013<\/strong>,&nbsp;<em>24<\/em>,&nbsp;920-937.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1055\/s-0032-1317804\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited account)<\/p>\n\n\n\n<p><strong>Conjugated Main Group Polymers for Optoelectronics<\/strong><br>X.-M. He, T. Baumgartner*<br><em>RSC Adv.<\/em>&nbsp;<strong>2013<\/strong>,&nbsp;<em>3<\/em>, 11334-11350. (<a href=\"http:\/\/dx.doi.org\/10.1039\/C3RA40286J\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited review,&nbsp;\u2018most accessed' in 07-08\/2013)<\/p>\n\n\n\n<p><strong>Dithiazolo[5,4-<em>b<\/em>:4',5'-<em>d<\/em>]phosphole: A highly luminescent electron-accepting building block<\/strong><br>X.-M. He, A. Y. Y. Woo, J. Borau-Garcia, T. Baumgartner*<br><em>Chem. Eur. J.&nbsp;<\/em><strong>2013<\/strong>,&nbsp;<em>19<\/em>, 7620-7630.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1002\/chem.201204375\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Molecular Engineering of the Physical Properties of Highly Luminescent&nbsp;<em>pi<\/em>-Conjugated Phospholes<\/strong><br>Y. Ren, F. Biegger, T. Baumgartner*<br><em>J. Phys. Chem. C<\/em>&nbsp;<strong>2013<\/strong>,&nbsp;<em>117<\/em>, 4748-4758. (<a href=\"http:\/\/dx.doi.org\/10.1021\/jp3115012\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Perfluorophenylene-Bridged Bisphospholes: Synthesis and Unexpected Photophysical Properties<\/strong><br>Y. Ren, A. Orthaber, R. Pietschnig,* T. Baumgartner*<br><em>Dalton Trans.<\/em>&nbsp;<strong>2013<\/strong>,&nbsp;<em>42<\/em>, 5314-5321. (<a href=\"http:\/\/dx.doi.org\/10.1039\/C3DT33058C\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Dithieno[3,2-<em>c<\/em>:2\u2019,3\u2019-<em>e<\/em>]-2,7-diketophosphepin: A Unique Building Block for Multifunctional&nbsp;<em>pi<\/em>-Conjugated Materials<\/strong><br>X.-M. He, J. Borau-Garcia, A. Y. Y. Woo, S. Trudel, T. Baumgartner*<br><em>J. Am. Chem. Soc.&nbsp;<\/em><strong>2013<\/strong>,&nbsp;<em>135<\/em>, 1137-1147.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1021\/ja310680x\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Phosphorus-Containing Polymers<\/strong>&nbsp;&nbsp;<br>Y.-y. Carpenter, T. Baumgartner*<br><em>Comprehensive Inorg.&nbsp;Chem. II Vol. 1&nbsp;<\/em>(Jan Reedijk and Kenneth Poeppelmeier, eds.), 893-932, Elsevier,&nbsp;Oxford&nbsp;<strong>2013<\/strong>.&nbsp;(<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/B9780080977744001315\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited book series chapter)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-14 kt-pane174_e15ac9-79\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><meta charset=\"utf-8\"><strong>201<\/strong>2<\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Charge-Transfer Properties of Lateral Triphenylamine-Dithienophosphole Diads<\/strong><br>C. J. Chua, Y. Ren, T. Baumgartner*<br><em>Org. Lett.&nbsp;<\/em><strong>2012<\/strong>,&nbsp;<em>14<\/em>, 1588-1591.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1021\/ol300331f\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(Highlighted in SYNFACTS 06\/2012)<\/p>\n\n\n\n<p><strong>Structure-Property Studies of Bichromophoric, PAH-Functionalized Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phospholes<\/strong><br>C. J. Chua, Y. Ren, T. Baumgartner*<br><em>Organometallics&nbsp;<\/em><strong>2012<\/strong>,&nbsp;<em>31<\/em>, 2425-2436.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1021\/om3000407\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Synthesis and Unexpected Halochromism of Carbazole-Functionalized Dithienophospholes<\/strong><br>M. Stolar, T. Baumgartner*<br><em>New J. Chem.&nbsp;<\/em><strong>2012<\/strong>,<em>&nbsp;36<\/em>, 1153-1160.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1039\/C2NJ40022G\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(<a href=\"http:\/\/pubs.rsc.org\/en\/journals\/journalissues\/nj#!issueid=nj036005&amp;type=current&amp;issnprint=1144-0546\">inside cover page<\/a>; 'most accessed' in 03\/2012)<\/p>\n\n\n\n<p><strong>Combining Form with Function: The Dawn of Phosphole-Based Functional Materials<\/strong><br>Y. Ren, T. Baumgartner*<br><em>Dalton Trans.<\/em>&nbsp;<strong>2012<\/strong>,&nbsp;<em>41<\/em>, 7792-7800.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1039\/c2dt00024e\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(Invited contribution for special issue \"New Talent Americas\"; 'most accessed' in 03\/2012)<\/p>\n\n\n\n<p><strong>Bio-Inspired Phosphole-Lipids: From Highly Fluorescent Organogels to Mechanically Responsive FRET<\/strong><br>Y. Ren, W. H. Kan, V. Thangadurai, T. Baumgartner*<br><em>Angew. Chem.<\/em>&nbsp;<strong>2012<\/strong>,&nbsp;<em>124<\/em>, 4031-4035;&nbsp;<em>Angew.&nbsp;Chem. Int. Ed.&nbsp;<\/em><strong>2012<\/strong>,&nbsp;<em>51<\/em>, 3964-3968.&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1002\/anie.201109205\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(Highlighted in the June 2012 issue of the Canadian Chemical News, ACCN)<\/p>\n\n\n\n<p><strong>Structure-Property Studies Toward the Stimuli-Responsive Behavior of Benzyl Phospholium Acenes<\/strong><br>Y. Ren, T. Baumgartner*<br><em>Inorg. Chem.&nbsp;<\/em><strong>2012<\/strong>,&nbsp;<em>51<\/em>, 2669-2678. (<a href=\"http:\/\/dx.doi.org\/10.1021\/ic2026335\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-15 kt-pane174_49c47b-0f\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2011<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>External-Stimuli Responsive Photophysics and Liquid Crystal Properties of Self-Assembled 'Phosphole-Lipids'<\/strong><br>Y. Ren, W. H. Kan, M. A. Henderson, P. G. Bomben, C. P. Berlinguette, V. Thangadurai, T. Baumgartner*<br><em>J. Am. Chem. Soc.&nbsp;<\/em><strong>2011<\/strong>,&nbsp;<em>133<\/em>, 17014-17026. (<a href=\"http:\/\/dx.doi.org\/10.1021\/ja206784f\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(highlighted under \"<a href=\"http:\/\/www.acs.org\/content\/acs\/en\/noteworthy-chemistry\/2011-archive\/noteworthy-chemistry-december-12-2011.html#P17_758\">Noteworthy Chemistry<\/a>\" on ACS website)<\/p>\n\n\n\n<p><strong>Room Temperature Multifunctional Organophosphorus Gels and Liquid Crystals<\/strong><br>C. Romero-Nieto, M. Marcos, S. Merino, J. Barber\u00e1, T. Baumgartner,* J. Rodr\u00edguez-L\u00f3pez*<br><em>Adv. Funct. Mater.&nbsp;<\/em><strong>2011<\/strong>,&nbsp;<em>21<\/em>, 4088-4099. (<a href=\"http:\/\/dx.doi.org\/10.1002\/adfm.201101219\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Dithienophosphole-Based Polythiophenes: A Versatile Scaffold For Luminescent Metal-Containing Polymers<\/strong><br>J. T. Wilson, T. Baumgartner*<br><em>ACS Polym. Preprints&nbsp;<\/em><strong>2011<\/strong>,&nbsp;<em>52<\/em>, 844-845.<\/p>\n\n\n\n<p><strong>Azadibenzophospholes - Functional Building Blocks with Pronounced Electron-Acceptor Character<\/strong><br>S. Durben, T. Baumgartner*<br><em>Inorg. Chem.&nbsp;<\/em><strong>2011<\/strong>,&nbsp;<em>50<\/em>, 3823-3836. (<a href=\"http:\/\/dx.doi.org\/10.1021\/ic200951x\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>3,7-Diazadibenzophosphole Oxide - A Phosphorus-Bridged Viologen-Analogue with Dramatically Lowered Reduction Threshold<\/strong><br>S. Durben, T. Baumgartner*<br><em>Angew.&nbsp;Chem.&nbsp;<\/em><strong>2011<\/strong>,&nbsp;<em>123<\/em>, 8096-8100;&nbsp;A<em>ngew. Chem. Int. Ed.&nbsp;<\/em><strong>2011<\/strong>,<em>&nbsp;50<\/em>, 7948-7952. (<a href=\"http:\/\/dx.doi.org\/10.1002\/anie.201102453\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Consolidation of Organometallic and Organic Chromophore Design Elements: Cyclometalated Ru(II) Complexes Functionalized with Triphenylamines<\/strong><br>K. C. D. Robson, B. D. Koivisto, A. Yella, B. Sporinaova, M. K. Nazeeruddin, T. Baumgartner, M. Gr\u00e4tzel, C. P. Berlinguette*<br><em>Inorg. Chem.&nbsp;<\/em><strong>2011<\/strong>,&nbsp;<em>50<\/em>, 5494-5508. (<a href=\"http:\/\/dx.doi.org\/10.1021\/ic200011m\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>End-Group Functionalization of Poly(3-hexylthiophene) as an Efficient Route to Photosensitize Nanocrystalline TiO<sub>2<\/sub>&nbsp;Films for Photovoltaic Applications\u201d<\/strong><br>R. A. Kr\u00fcger, T. J. Gordon, T. Baumgartner,* T. C. Sutherland*<br><em>ACS Appl. Mater. &amp; Interfaces&nbsp;<\/em><strong>2011<\/strong>,&nbsp;<em>3<\/em>, 2031-2041. (<a href=\"http:\/\/dx.doi.org\/10.1021\/am200262w\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Dually Switchable Heterotetracenes - Addressing the Photophysical Properties and Self-Organization of the P-S-System<\/strong><br>Y. Ren, T. Baumgartner*<br><em>J. Am. Chem. Soc.&nbsp;<\/em><strong>2011<\/strong>,<em>&nbsp;133<\/em>, 1328-1340. (<a href=\"http:\/\/dx.doi.org\/10.1021\/ja108081b\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Band-Gap Engineering of Polythiophenens via Dithienophosphole-Doping<\/strong><br>R. A. Kr\u00fcger, T. J. Gordon, T. C. Sutherland,* T. Baumgartner*<br><em>J. Polym. Sci. Part A: Polym. Chem.&nbsp;<\/em><strong>2011<\/strong>,&nbsp;<em>49<\/em>, 1201-1209. (<a href=\"http:\/\/dx.doi.org\/10.1002\/pola.24538\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-16 kt-pane174_c00a87-0c\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2010<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Synthesis of pi-Extended Thiadiazole (Oxides) and Their Electronic Properties<\/strong><br>T. Linder, E. Badiola, T. Baumgartner,* T. C. Sutherland*<br><em>Org. Lett.&nbsp;<\/em><strong>2010<\/strong>,&nbsp;<em>12<\/em>, 4520-4523. (<a href=\"http:\/\/dx.doi.org\/10.1021\/ol1018213\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Synthesis and Photophysical Properties of Donor-Acceptor Dithienophospholes<\/strong><br>C. Romero-Nieto, K. Kamada, D. T. Cramb, S. Merino, J. Rodr\u00edguez-L\u00f3pez,* T. Baumgartner*<br><em>Eur. J. Org. Chem.&nbsp;<\/em><strong>2010<\/strong>, 5225-5231. (<a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201000574\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Synthesis and Photophysical Properties of Bipyridine-Extended Dithienophosphole Chromophores for Transition Metal Complexation<\/strong><br>D. R. Bai, T. Baumgartner*<br><em>Organometallics<\/em>&nbsp;<strong>2010<\/strong>,&nbsp;<em>29<\/em>, 3289-3297. (<a href=\"http:\/\/dx.doi.org\/10.1021\/om100421w\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Triphenylamine-Modified Ruthenium(II) Terpyridine Complexes: Enhancement of Light Absorption by Conjugated Bridging Motifs<\/strong><br>K. C. D. Robson, B. D. Koivisto, T. J. Gordon, T. Baumgartner, C. P. Berlinguette*<br><em>Inorg. Chem.&nbsp;<\/em><strong>2010<\/strong>,&nbsp;<em>49<\/em>, 5335-5337. (<a href=\"http:\/\/dx.doi.org\/10.1021\/ic9025427\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Solution growth of anatase TiO<sub>2<\/sub>&nbsp;nanowires from transparent conducting glass substrates<\/strong><br>P. A. Sedach, T. J. Gordon, S. Y. Sayed, T. Fuerstenhaupt, R. Sui, T. Baumgartner, C. P. Berlinguette*<br><em>J. Mater. Chem.&nbsp;<\/em><strong>2010<\/strong>,&nbsp;<em>20<\/em>, 5063-5069. (<a href=\"http:\/\/dx.doi.org\/10.1039\/c0jm00266f\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Extended 2,5-Diazaphosphole Oxides \u2013 Promising Electron Acceptor Building Blocks for&nbsp;<em>pi<\/em>-Conjugated Organic Materials<\/strong><br>T. Linder, T. C. Sutherland,* T. Baumgartner*<br><em>Chem. Eur. J.<\/em>&nbsp;<strong>2010<\/strong>,&nbsp;<em>16<\/em>, 7101-7105. (<a href=\"http:\/\/dx.doi.org\/10.1002\/chem.201000382\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Ladder-Type pi-Conjugated 4-Hetero-1,4-Dihydrophosphinines - A Structure-Property ¿ì²¥ÊÓƵ<\/strong><br>Y. Ren, T. Baumgartner*<br><em>Chem. Asian J.&nbsp;<\/em><strong>2010<\/strong>,&nbsp;<em>5<\/em>, 1918-1929. (<a href=\"http:\/\/dx.doi.org\/10.1002\/asia.201000196\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>('most accessed' in 06\/2010 list)<\/p>\n\n\n\n<p><strong>Structure-Property Relationships of Acylated Asymmetric Dithienophospholes<\/strong><br>T. J. Gordon, L. D. Szabo, T. Linder, C. P. Berlinguette, T. Baumgartner*<br><em>C.R. Chimie&nbsp;<\/em><strong>2010<\/strong>,&nbsp;<em>13<\/em>, 971-979. (<a href=\"http:\/\/dx.doi.org\/10.1016\/j.crci.2010.04.023\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited contribution for special issue \"Phosphorus Chemistry Today\")<\/p>\n\n\n\n<p><strong>Dithienophosphole-capped&nbsp;<em>pi<\/em>-Conjugated Oligomers<\/strong><br>S. Durben, T. Linder, T. Baumgartner*<br><em>New J. Chem.<\/em>&nbsp;<strong>2010<\/strong>,<em>&nbsp;34<\/em>, 1585-1592. (<a href=\"http:\/\/dx.doi.org\/10.1039\/c0nj00026d\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited contribution for special issue on main group chemistry)<\/p>\n\n\n\n<p><strong>Metal-Rich Organometallics<\/strong><br>R. A. Kr\u00fcger, T. Baumgartner*<br><em>Dalton Trans.&nbsp;<\/em><strong>2010<\/strong>,&nbsp;<em>39<\/em>, 5759-5767. (<a href=\"http:\/\/dx.doi.org\/10.1039\/b925709h\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited perspective &amp;&nbsp;<a href=\"http:\/\/www.rsc.org\/delivery\/_ArticleLinking\/DisplayArticleForFree.cfm?doi=c005412g&amp;JournalCode=DT\" target=\"_blank\" rel=\"noreferrer noopener\">inside cover page<\/a>)<\/p>\n\n\n\n<p><strong>Trendbericht Anorganische Chemie 2009: Hauptgruppenchemie<\/strong><br>T. Baumgartner,* R. Pietschnig*<br><em>Nachr. Chem.&nbsp;<\/em><strong>2010<\/strong>,&nbsp;<em>58<\/em>, 239-249. (<a href=\"http:\/\/dx.doi.org\/10.1002\/nadc.201068240\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Highly Luminescent Terpyridinyl-ethynyl Functionalized Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phospholes: Synthesis, Properties and Complexation Behavior<\/strong><br>D. R. Bai, C. Romero-Nieto, T. Baumgartner*<br><em>Dalton Trans.&nbsp;<\/em><strong>2010<\/strong>,&nbsp;<em>39<\/em>, 1250-1260. (<a href=\"http:\/\/dx.doi.org\/10.1039\/b919718d\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-17 kt-pane174_ff6901-00\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2009<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Simple and Efficient Generation of White Light-Emission From Organophosphorus Building Blocks<\/strong><br>C. Romero-Nieto, S. Durben, I. M. Kormos, T. Baumgartner*<br><em>Adv. Funct. Mater.<\/em>&nbsp;<strong>2009<\/strong>,&nbsp;<em>14<\/em>, 3625-3631. (<a href=\"http:\/\/dx.doi.org\/10.1002\/adfm.200901540\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>('most accessed' list 10\/2009; part of a virtual 'hot topic' issue issue on organic electronics 10-11\/2009)<\/p>\n\n\n\n<p><strong>Synthesis and Properties of Ladder-type 1,4-Dihydro-1,4-phosphasilins<\/strong><br>Y. Ren, T. Linder, T. Baumgartner*<br><em>Can. J. Chem.<\/em>&nbsp;<strong>2009<\/strong>,&nbsp;<em>87<\/em>, 1222-1229. (<a href=\"http:\/\/dx.doi.org\/10.1139\/V09-108\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Dendrimeric OPV-Extended Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phospholes \u2013 Synthesis, Self-Organization and Optical Properties<\/strong><br>C. Romero-Nieto, S. Merino, J. Rodr\u00edguez-L\u00f3pez,* T. Baumgartner*<br><em>Chem. Eur. J.&nbsp;<\/em><strong>2009<\/strong>,&nbsp;<em>15<\/em>, 4135-4145. (<a href=\"http:\/\/dx.doi.org\/10.1002\/chem.200802482\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Fluorinated Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phospholes with Highly Stabilized LUMO Levels<\/strong><br>Y. Ren, Y. Dienes, S. Hettel, M. Parvez, B. Hoge,* T. Baumgartner*<br><em>Organometallics&nbsp;<\/em><strong>2009<\/strong>,&nbsp;<em>28<\/em>, 734-740. (<a href=\"http:\/\/dx.doi.org\/10.1021\/om800874d\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>2,6-Bis(tributyltin)benzo[1,2-<em>b<\/em>:5,4-<em>b<\/em>\u2019]dithiophene: A New Synthon for Organic Semiconductors<\/strong><br>M. P. Boone, Y. Dienes, T. Baumgartner*<br><em>Arkivoc&nbsp;<\/em><strong>2009<\/strong>,&nbsp;<em>(v)<\/em>, 90-101. (<a href=\"http:\/\/www.arkat-usa.org\/get-file\/27101\/\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(commemorative issue for Ted Sorensen)<\/p>\n\n\n\n<p><strong>Tuning the Photophysical Properties and Solid-State Organization of Perfluorophenyl-functionalized Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phospholes<\/strong><br>Y. Dienes, U. Englert, T. Baumgartner*<br><em>Z. Anorg. Allg. Chem.<\/em>&nbsp;<strong>2009<\/strong>,&nbsp;<em>635<\/em>, 238-244. (<a href=\"http:\/\/dx.doi.org\/10.1002\/zaac.200800425\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(commemorative section for Edgar Niecke)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-18 kt-pane174_c82bde-68\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2008<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Toward Low-Band Gap Dithienophosphole Copolymers for Application in Organic Solar Cells<\/strong><br>S. Durben, D. Nickel, R. A. Kr\u00fcger, T. C. Sutherland, T. Baumgartner*<br><em>J. Polym. Sci. Part A: Polym. Chem.<\/em>&nbsp;<strong>2008<\/strong>,&nbsp;<em>46<\/em>, 8179-8190. (<a href=\"http:\/\/dx.doi.org\/10.1002\/pola.23115\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Phosphorus-Based Heteropentacenes: Efficiently Tunable Materials for Organic&nbsp;<em>n<\/em>-Type Semiconductors<\/strong><br>Y. Dienes, M. Eggenstein, T. K\u00e1rp\u00e1ti, T. C. Sutherland, L. Nyul\u00e1szi,* T. Baumgartner*<br><em>Chem. Eur. J.&nbsp;<\/em><strong>2008<\/strong>,&nbsp;<em>14<\/em>, 9878-9889. (<a href=\"http:\/\/dx.doi.org\/10.1002\/chem.200801549\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(highlighted with an invited&nbsp;<a href=\"http:\/\/onlinelibrary.wiley.com\/journal\/10.1002\/(ISSN)1521-3765\/homepage\/frontisp\/2008\/32_801549.html\" target=\"_blank\" rel=\"noreferrer noopener\">frontispiece<\/a>)<\/p>\n\n\n\n<p><strong>A New Polymorph of Dimesitylborinic Acid<\/strong><br>M. Kuhlmann, T. Baumgartner, M. Parvez*<br><em>Acta Cryst. E&nbsp;<\/em><strong>2008<\/strong>,&nbsp;<em>64<\/em>, o1185. (<a href=\"http:\/\/dx.doi.org\/10.1107\/S1600536808015638\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-19 kt-pane174_98f5ce-11\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2007<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Selective Tuning of the Band-Gap of pi-Conjugated Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phospholes Toward Different Emission Colors<\/strong><br>Y. Dienes, S. Durben, T. K\u00e1rp\u00e1ti, T. Neumann, U. Englert, L. Nyul\u00e1szi,* T. Baumgartner*<br><em>Chem. Eur. J.&nbsp;<\/em><strong>2007<\/strong>,&nbsp;<em>13<\/em>, 7487-7500. (<a href=\"http:\/\/dx.doi.org\/10.1002\/chem.200700399\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>A Reference for a Rapidly Growing Field<\/strong><br>T. Baumgartner<br><em>Adv. Synth. Catal.&nbsp;<\/em><strong>2007<\/strong>,&nbsp;<em>349<\/em>, 1811-1812. (<a href=\"http:\/\/dx.doi.org\/10.1002\/adsc.200700257\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(Book Review: Functional Organic Materials, Wiley-VCH)<\/p>\n\n\n\n<p><strong>Recent Developments in Phosphole-Containing Oligo- and Polythiophene Materials<\/strong><br>M.G. Hobbs, T. Baumgartner*<br><em>Eur. J. Inorg. Chem.<\/em>&nbsp;<strong>2007<\/strong>, 3611-3628. (<a href=\"http:\/\/dx.doi.org\/10.1002\/ejic.200700236\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited microreview &amp;&nbsp;<a href=\"http:\/\/onlinelibrary.wiley.com\/journal\/10.1002\/(ISSN)1099-0682c\/homepage\/cover\/2007_2007_23.html\" target=\"_blank\" rel=\"noreferrer noopener\">cover page<\/a>; 'most cited' list)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-20 kt-pane174_e10fdc-73\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2006<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Cationic Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phospholes: A New Building Block for Luminescent Conjugated Polyelectrolytes<\/strong><br>S. Durben, Y. Dienes, T. Baumgartner*<br><em>Org. Lett.&nbsp;<\/em><strong>2006<\/strong>,&nbsp;<em>8<\/em>, 5893-5896. (<a href=\"http:\/\/dx.doi.org\/10.1021\/ol062580w\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Organophosphorus&nbsp;<em>pi<\/em>-conjugated materials<\/strong><br>T. Baumgartner,* R. R\u00e9au*<br><em>Chem. Rev.&nbsp;<\/em><strong>2006<\/strong>,&nbsp;<em>106<\/em>, 4681-4727. (<a href=\"http:\/\/dx.doi.org\/10.1021\/cr040179m\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited review)<\/p>\n\n\n\n<p><strong>Redox-Active, Multinuclear (Ferrocenylethynyl)phosphanes and Their Palladium and Platinum Complexes<\/strong><br>T. Baumgartner,* M. Fiege, F. Pontzen, R. Arteaga-M\u00fcller<br><em>Organometallics&nbsp;<\/em><strong>2006<\/strong>,&nbsp;<em>25<\/em>, 5657-5664. (<a href=\"http:\/\/dx.doi.org\/10.1021\/om0606892\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Synthesis and optoelectronic properties of transition metal complexes incorporating dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phosphole ligands<\/strong><br>Y. Dienes, M. Eggenstein, T. Neumann, U. Englert, T. Baumgartner*<br><em>Dalton Trans.&nbsp;<\/em><strong>2006<\/strong>, 1424-1433. (<a href=\"http:\/\/dx.doi.org\/10.1039\/b509277a\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Synthesis and Unexpected Reactivity of Si-H Functionalized Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phospholes<\/strong>&nbsp;<br>T. Baumgartner,* W. Wilk<br><em>Org. Lett.<\/em>&nbsp;<strong>2006<\/strong>,&nbsp;<em>8<\/em>, 503-506. (<a href=\"http:\/\/dx.doi.org\/10.1021\/ol0529288\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n\n\n\n<p><strong>Highly sensitive sensory materials for fluoride ions based on the dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phosphole system<\/strong><br>T. Neumann, Y. Dienes, T. Baumgartner*<br><em>Org. Lett.&nbsp;<\/em><strong>2006<\/strong>,&nbsp;<em>8<\/em>, 495-497. (<a href=\"http:\/\/dx.doi.org\/10.1021\/ol052911p\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>('most cited articles in 2006' list)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-21 kt-pane174_22d284-8a\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2005<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong><em>pi<\/em>-Conjugated heterocyclic fused bithiophene materials<\/strong><br>T. Baumgartner<br><em>J. Inorg. Organomet. Poly. Mater.&nbsp;<\/em><strong>2005<\/strong>,&nbsp;<em>15<\/em>, 389-409. (<a href=\"http:\/\/dx.doi.org\/10.1007\/s10904-006-9013-3\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br>(invited review)<\/p>\n\n\n\n<p><strong>From Model Compounds to Extended&nbsp;<em>pi<\/em>-Conjugated Systems: Synthesis and Properties of Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phospholes<\/strong><br>T. Baumgartner,* W. Bergmans, T. K\u00e1rp\u00e1ti, T. Neumann, M. Nieger, L. Nyul\u00e1szi*<br><em>Chem. Eur. J.&nbsp;<\/em><strong>2005<\/strong>,&nbsp;<em>11<\/em>, 4687-4699. (<a href=\"http:\/\/dx.doi.org\/10.1002\/chem.200500152\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)&nbsp;<\/p>\n\n\n\n<p><strong>Synthesis and X-ray single-crystal structure study of 5,5'-bis(silyl)-functionalized 3,3'-dibromo-2,2'-dithiophenes<\/strong><br>T. Baumgartner<br><em>Appl. Organomet. Chem.<\/em>&nbsp;<strong>2005<\/strong>,&nbsp;<em>19<\/em>, 859-863. (<a href=\"http:\/\/dx.doi.org\/10.1002\/aoc.917\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-22 kt-pane174_26dd4a-87\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2004<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>The Dithieno[3,2-<em>b<\/em>:2\u2019,3\u2019-<em>d<\/em>]phosphole System: A Novel Building Block for Highly Luminescent&nbsp;<em>pi<\/em>-Conjugated Materials<\/strong><br>T. Baumgartner,* T. Neumann, B. Wirges<br><em>Angew. Chem.&nbsp;<\/em><strong>2004<\/strong>,&nbsp;<em>116<\/em>, 6323-6328;&nbsp;<em>Angew. Chem. Int. Ed.<\/em><strong>2004<\/strong>,&nbsp;<em>43<\/em>, 6197-6201. (<a href=\"http:\/\/dx.doi.org\/10.1002\/anie.200461301\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-23 kt-pane174_04710c-b6\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>2003<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><strong>Synthesis and Properties of New Phosphorus-Functionalized Bithiophene Materials<\/strong><br>T. Baumgartner<br><em>Macromol. Symp.&nbsp;<\/em><strong>2003<\/strong>,&nbsp;<em>196<\/em>, 279-288. (<a href=\"http:\/\/dx.doi.org\/10.1002\/masy.200390167\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-kadence-pane kt-accordion-pane kt-accordion-pane-24 kt-pane174_52403a-a7\"><div class=\"kt-accordion-header-wrap\"><button class=\"kt-blocks-accordion-header kt-acccordion-button-label-show\" type=\"button\"><span class=\"kt-blocks-accordion-title-wrap\"><span class=\"kt-blocks-accordion-title\"><strong>Papers from PhD and PDF<\/strong><\/span><\/span><span class=\"kt-blocks-accordion-icon-trigger\"><\/span><\/button><\/div><div class=\"kt-accordion-panel kt-accordion-panel-hidden\"><div class=\"kt-accordion-panel-inner\">\n<p><br><strong>Bis{mu-1,4-bis[(diphenylphosphanyl)ethynyl]benzene-k<sup>2<\/sup>P:P\u2019}bis[transdiiodidopalladium(II)] chloroform trisolvate<\/strong>&nbsp;<br>W. Y. Chan, T. Baumgartner, A. J. Lough, I. Manners*<br><em>Acta Cryst. E&nbsp;<\/em><strong>2007<\/strong>,&nbsp;<em>63<\/em>, M2886-U293. (<a href=\"http:\/\/dx.doi.org\/10.1107\/S160053680704620X\">link<\/a>)&nbsp; &nbsp;<\/p>\n\n\n\n<p><strong>Metallochain Cluster Complexes and Metallomacrocyclic Triangles Based on Coordination Bonds between Palladium or Platinum and&nbsp;Diphosphinoacetylene Ligands<\/strong>&nbsp;<br>T. Baumgartner, K. Huynh, S. Schleidt, A. J. Lough, I. Manners*<br><em>Chem. Eur. J.<\/em>&nbsp;<strong>2002<\/strong>,&nbsp;<em>8<\/em>, 4622-4632. (<a href=\"http:\/\/dx.doi.org\/10.1002\/1521-3765%2820021018%298:20%3C4622::AID-CHEM4622%3E3.0.CO;2-V\">link<\/a>)&nbsp; &nbsp;&nbsp;<\/p>\n\n\n\n<p><strong>Nucleophilically Assisted and Cationic Ring-Opening Polymerization (ROP) of Tin-bridged [1]ferrocenophanes<\/strong>&nbsp;<br>T. Baumgartner, F. J\u00e4kle, R. Rulkens, G. Zech, A. J. Lough, I. Manners*<br><em>J. Am. Chem. Soc.<\/em>&nbsp;<strong>2002<\/strong>,&nbsp;<em>124<\/em>, 10062-10070&nbsp;(<a href=\"http:\/\/dx.doi.org\/10.1021\/ja020206v\">link<\/a>)<\/p>\n\n\n\n<p><strong>Unusual Approaches to Organophosphorus Compounds - The Surprising Reactivity of Bis(methylene)phosphoranes and Related&nbsp;Phosphoranylidene Carbenoids<\/strong>&nbsp;<br>T. Baumgartner, P. Moors, M. Nieger, H. Hupfer, E. Niecke*<br><em>Organometallics&nbsp;<\/em><strong>2002<\/strong>,&nbsp;<em>21<\/em>, 4919-4926. (<a href=\"http:\/\/dx.doi.org\/10.1021\/om020319n\">link<\/a>)<\/p>\n\n\n\n<p><strong>Phosphavinylidene carbenoids [P]=C(Li)X (X=Br,Cl,F): Structure and dynamics<\/strong><br>T. Baumgartner, D. Gudat, M. Nieger, E. Niecke*<br><em>Phosphorus, Sulfur &amp; Silicon&nbsp;<\/em><strong>1999<\/strong>,&nbsp;<em>147<\/em>, 25. (<a href=\"http:\/\/dx.doi.org\/10.1080\/10426509908053493\">link<\/a>)<\/p>\n\n\n\n<p><strong>Lithium Phosphoranylidene Carbenoides Mes*-P(=E)=C(X)Li(THF)<sub>3<\/sub>&nbsp;(E=NMes*, C(SiMe<sub>3<\/sub>)<sub>2<\/sub>, X=Br,Cl,F): Synthesis, and Structural Investigations&nbsp;in Solution and Solid&nbsp;State&nbsp;<\/strong><br>T. Baumgartner, D.Gudat,* E. Niecke,* M. Nieger, T. Schiffer<br><em>J. Am. Chem. Soc.&nbsp;<\/em><strong>1999<\/strong>,&nbsp;<em>121<\/em>, 5953-5960. (<a href=\"http:\/\/dx.doi.org\/10.1021\/ja990074e\">link<\/a>)<\/p>\n\n\n\n<p><strong>Lithium Phosphoranylidene Ylides Mes*-P(=E)=C(H)Li(THF)<sub>3<\/sub>&nbsp;(E=NMes*,(SiMe<sub>3<\/sub>)<sub>2<\/sub>)-Synthesis, Crystal Structure, and Transmetalation<\/strong><br>T. Baumgartner, B. Schinkels, D. Gudat,* M. Nieger, E. Niecke*<br><em>J. Am. Chem. Soc.<\/em>&nbsp;<strong>1997<\/strong>,&nbsp;<em>119<\/em>, 12410-12411. (<a href=\"http:\/\/dx.doi.org\/10.1021\/ja9718127\">link<\/a>)<\/p>\n<\/div><\/div><\/div>\n<\/div><\/div><\/div>\n\n\n\n<div style=\"height:100px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<div class=\"wp-block-columns social-bar-block is-layout-flex wp-container-core-columns-is-layout-9d6595d7 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<h2 class=\"wp-block-heading h6 text-white text-center\">Baumgartner Research Group - Last updated 03\/2026<\/h2>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<ul class=\"wp-block-social-links is-layout-flex wp-block-social-links-is-layout-flex\"><li class=\"wp-social-link wp-social-link-bluesky  wp-block-social-link\"><a href=\"https:\/\/bsky.app\/profile\/tbaumlab.bsky.social\" class=\"wp-block-social-link-anchor\"><svg width=\"24\" height=\"24\" viewBox=\"0 0 24 24\" version=\"1.1\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" aria-hidden=\"true\" focusable=\"false\"><path d=\"M6.3,4.2c2.3,1.7,4.8,5.3,5.7,7.2.9-1.9,3.4-5.4,5.7-7.2,1.7-1.3,4.3-2.2,4.3.9s-.4,5.2-.6,5.9c-.7,2.6-3.3,3.2-5.6,2.8,4,.7,5.1,3,2.9,5.3-5,5.2-6.7-2.8-6.7-2.8,0,0-1.7,8-6.7,2.8-2.2-2.3-1.2-4.6,2.9-5.3-2.3.4-4.9-.3-5.6-2.8-.2-.7-.6-5.3-.6-5.9,0-3.1,2.7-2.1,4.3-.9h0Z\"><\/path><\/svg><span class=\"wp-block-social-link-label screen-reader-text\">Bluesky<\/span><\/a><\/li>\n\n<li class=\"wp-social-link wp-social-link-chain  wp-block-social-link\"><a href=\"https:\/\/www.yorku.ca\/science\/chemistry\/\" class=\"wp-block-social-link-anchor\"><svg width=\"24\" height=\"24\" viewBox=\"0 0 24 24\" version=\"1.1\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" aria-hidden=\"true\" focusable=\"false\"><path d=\"M15.6,7.2H14v1.5h1.6c2,0,3.7,1.7,3.7,3.7s-1.7,3.7-3.7,3.7H14v1.5h1.6c2.8,0,5.2-2.3,5.2-5.2,0-2.9-2.3-5.2-5.2-5.2zM4.7,12.4c0-2,1.7-3.7,3.7-3.7H10V7.2H8.4c-2.9,0-5.2,2.3-5.2,5.2,0,2.9,2.3,5.2,5.2,5.2H10v-1.5H8.4c-2,0-3.7-1.7-3.7-3.7zm4.6.9h5.3v-1.5H9.3v1.5z\"><\/path><\/svg><span class=\"wp-block-social-link-label screen-reader-text\">Link<\/span><\/a><\/li><\/ul>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Our book on&nbsp;\u201cMain Group Strategies towards Functional Hybrid Materials\u201d&nbsp;(Editors T. Baumgarter and F. J\u00e4kle; ISBN: 978-1-119-23597-2) is now available&nbsp;here<\/p>\n","protected":false},"author":45,"featured_media":1500,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_kad_blocks_custom_css":"","_kad_blocks_head_custom_js":"","_kad_blocks_body_custom_js":"","_kad_blocks_footer_custom_js":"","ngg_post_thumbnail":0,"footnotes":""},"tags":[],"class_list":["post-174","page","type-page","status-publish","has-post-thumbnail","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Publications | Baumgartner Research Group<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.yorku.ca\/science\/research\/tbaumgar\/publications\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Publications | Baumgartner Research Group\" \/>\n<meta property=\"og:description\" content=\"Our book on&nbsp;\u201cMain Group Strategies towards Functional Hybrid Materials\u201d&nbsp;(Editors T. 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