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Stolar M, Baumgartner T. Functional conjugated pyridines via main-group element tuning. Chem Commun (Camb). 2018;54(27):3311-3322doi: 10.1039/c8cc00373d.
Stolar, M., & Baumgartner, T. (2018). Functional conjugated pyridines via main-group element tuning. Chemical communications (Cambridge, England), 54(27), 3311-3322. https://doi.org/10.1039/c8cc00373d
Stolar, Monika, and Baumgartner, Thomas. "Functional conjugated pyridines via main-group element tuning." Chemical communications (Cambridge, England) vol. 54,27 (2018): 3311-3322. doi: https://doi.org/10.1039/c8cc00373d
Stolar M, Baumgartner T. Functional conjugated pyridines via main-group element tuning. Chem Commun (Camb). 2018 Mar 29;54(27):3311-3322. doi: 10.1039/c8cc00373d. PMID: 29517790.
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Chem Commun (Camb). 2018 Mar 29;54(27):3311-3322. doi: 10.1039/c8cc00373d.

Functional conjugated pyridines via main-group element tuning.

Chemical communications (Cambridge, England)

Monika Stolar, Thomas Baumgartner

Affiliations

  1. Department of Chemistry, York University, 4700 Keele St., Toronto, ON M3J 1P3, Canada. [email protected].

PMID: 29517790 DOI: 10.1039/c8cc00373d

Abstract

Pyridine-based materials have seen widespread attention for the development of n-type organic materials. In recent years, the incorporation of main-group elements has also explored significant advantages for the development and tunability of organic conjugated materials. The unique chemical and electronic structure of main-group elements has led to several enhancements in conventional organic materials. This Feature article highlights recent main-group based pyridine materials by discussing property enhancements and application in organic electronics.

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