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Free Radical Chemistry of Phosphasilenes.


ABSTRACT: Understanding the characteristics of radicals formed from silicon-containing heavy analogues of alkenes is of great importance for their application in radical polymerization. Steric and electronic substituent effects in compounds such as phosphasilenes not only stabilize the Si=P double bond, but also influence the structure and species of the formed radicals. Herein we report our first investigations of radicals derived from phosphasilenes with Mes, Tip, Dur, and NMe2 substituents on the P atom, using muon spin spectroscopy and DFT calculations. Adding muonium (a light isotope of hydrogen) to phosphasilenes reveals that: a)?the electron-donor NMe2 and the bulkiest Tip-substituted phosphasilenes form several muoniated radicals with different rotamer conformations; b)?bulky Dur-substituted phosphasilene forms two radicals (Si- and P-centred); and c)?Mes-substituted phosphasilene mainly forms one species of radical, at the P centre. These significant differences result from intramolecular substituent effects.

SUBMITTER: Samedov K 

PROVIDER: S-EPMC7540504 | biostudies-literature | 2020 Sep

REPOSITORIES: biostudies-literature

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Free Radical Chemistry of Phosphasilenes.

Samedov Kerim K   Heider Yannic Y   Cai Yuanjing Y   Willmes Philipp P   Mühlhausen Daniel D   Huch Volker V   West Robert R   Scheschkewitz David D   Percival Paul W PW  

Angewandte Chemie (International ed. in English) 20200709 37


Understanding the characteristics of radicals formed from silicon-containing heavy analogues of alkenes is of great importance for their application in radical polymerization. Steric and electronic substituent effects in compounds such as phosphasilenes not only stabilize the Si=P double bond, but also influence the structure and species of the formed radicals. Herein we report our first investigations of radicals derived from phosphasilenes with Mes, Tip, Dur, and NMe<sub>2</sub> substituents o  ...[more]

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