Unknown

Dataset Information

0

Well-Defined, Molecular Bismuth Compounds: Catalysts in Photochemically Induced Radical Dehydrocoupling Reactions.


ABSTRACT: A series of diorgano(bismuth)chalcogenides, [Bi(di-aryl)EPh], has been synthesised and fully characterised (E=S, Se, Te). These molecular bismuth complexes have been exploited in homogeneous photochemically-induced radical catalysis, using the coupling of silanes with TEMPO as a model reaction (TEMPO=(tetramethyl-piperidin-1-yl)-oxyl). Their catalytic properties are complementary or superior to those of known catalysts for these coupling reactions. Catalytically competent intermediates of the reaction have been identified. Applied analytical techniques include NMR, UV/Vis, and EPR spectroscopy, mass spectrometry, single-crystal X-ray diffraction analysis, and (TD)-DFT calculations.

SUBMITTER: Ramler J 

PROVIDER: S-EPMC7821184 | biostudies-literature | 2020 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Well-Defined, Molecular Bismuth Compounds: Catalysts in Photochemically Induced Radical Dehydrocoupling Reactions.

Ramler Jacqueline J   Krummenacher Ivo I   Lichtenberg Crispin C  

Chemistry (Weinheim an der Bergstrasse, Germany) 20201014 64


A series of diorgano(bismuth)chalcogenides, [Bi(di-aryl)EPh], has been synthesised and fully characterised (E=S, Se, Te). These molecular bismuth complexes have been exploited in homogeneous photochemically-induced radical catalysis, using the coupling of silanes with TEMPO as a model reaction (TEMPO=(tetramethyl-piperidin-1-yl)-oxyl). Their catalytic properties are complementary or superior to those of known catalysts for these coupling reactions. Catalytically competent intermediates of the re  ...[more]

Similar Datasets

| S-EPMC4832830 | biostudies-other
| S-EPMC5399632 | biostudies-literature
| S-EPMC4531818 | biostudies-other
| S-EPMC6071431 | biostudies-literature
| S-EPMC6695427 | biostudies-literature
| S-EPMC4464534 | biostudies-literature
| S-EPMC5656039 | biostudies-literature
| S-EPMC5341381 | biostudies-literature
| S-EPMC3366164 | biostudies-literature
| S-EPMC4195373 | biostudies-literature