| Literature DB >> 22730141 |
Kazuhiko Nagura1, Shohei Saito, Roland Fröhlich, Frank Glorius, Shigehiro Yamaguchi.
Abstract
Give and take: The introduction of NHC-borane moieties to thiophene-based π skeletons endows a zwitterionic character, which makes the π system electron-donating, while the NHC ring acts as an electron-accepting moiety. The NHC-borane-substituted thiophene underwent a clean photoisomerization with a drastic color change, however, the expanded bithiophene derivatives were inert to this photoreaction, showed low oxidation potentials, and formed a slipped π-stacked array in the crystal.Entities:
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Year: 2012 PMID: 22730141 DOI: 10.1002/anie.201204050
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336