Thomas Baumgartner, Ph.D.

Affiliations: 
2013-2010 Chemistry University of Calgary, Calgary, Alberta, Canada 
 2017- Chemistry York University, Toronto, Ontario, Canada 
Area:
Main-group, Organic Materials Chemistry, and Sustainable Energy
Website:
http://www.yorku.ca/tbaumgar/people/tbaumgar/
Google:
"Thomas Baumgartner"
Bio:

http://www.yorku.ca/tbaumgar/people/tbaumgar/
http://www.chem.ucalgary.ca/research/groups/ttbaumga/

Mean distance: 8.88
 
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Parents

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Edgar Niecke grad student 1998 Universität Bonn
 (C-functionalized bis(methylene)phosphoranes: Interesting building blocks for the stabilization of reactive intermediates.)
Ian Manners post-doc 2002 University of Toronto
Jun Okuda research scientist RWTH Aachen University
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Publications

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Yang Z, Li X, Yang K, et al. (2022) Tailored Solvatochromic NIR Phosphorus-Chromophores via Selective P-N and P-C Chemistry in P-Heteropines. Organic Letters. 24: 2045-2049
Bridges CR, Borys AM, Béland VA, et al. (2020) Phosphoryl- and phosphonium-bridged viologens as stable two- and three-electron acceptors for organic electrodes. Chemical Science. 11: 10483-10487
Bridges CR, Borys AM, Béland VA, et al. (2020) Phosphoryl- and phosphonium-bridged viologens as stable two- and three-electron acceptors for organic electrodes Chemical Science
Bridges CR, Baumgartner T. (2020) Lewis acids and bases as molecular dopants for organic semiconductors Journal of Physical Organic Chemistry. 33
Gaffen JR, Bentley JN, Torres LC, et al. (2019) A Simple and Effective Method of Determining Lewis Acidity by Using Fluorescence Chem. 5: 1567-1583
Berville M, Richard J, Stolar M, et al. (2018) A Highly Stable Organic Radical Cation. Organic Letters
Stolar M, Baumgartner T. (2018) Functional conjugated pyridines via main-group element tuning. Chemical Communications (Cambridge, England)
Grenon N, Baumgartner T. (2018) Exploration of Hypervalent Lewis Acid/Base Interactions in 2-(2'-Thiazolyl)-3-thienylphosphanes. Inorganic Chemistry
Wang Z, Spasyuk D, Baumgartner T. (2018) On the reactivity of P-chloro dithieno[3,2-b:2′,3′-d]phosphole oxide Canadian Journal of Chemistry. 96: 555-560
Welsh TA, Laventure A, Baumgartner T, et al. (2018) Dithienophosphole-based molecular electron acceptors constructed using direct (hetero)arylation cross-coupling methods Journal of Materials Chemistry C. 6: 2148-2154
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