Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1132
Title: Phenylene-bridged cross-conjugated 1,2,3-trisilacyclopentadienes
Authors: Zhao, Hui
Klemmer, Lukas
Cowley, Michael J.
MAJUMDAR, MOUMITA
Huch, Volker
Zimmer, Michael
Scheschkewitz, David
Dept. of Chemistry
Keywords: Group 14 elements
Molecular-Orbital Methods
Double-Bonds
Disilenyl silylene
Crystal-Structure
Stable disilenes
Multiple bonds
SI=SI Bonds
Basis-sets
TOC-AUG-2018
2018
Issue Date: Aug-2018
Publisher: Royal Society of Chemistry
Citation: Chemical Communications. Vol. 54(60).
Abstract: 1,2,3-Trisilacyclopentadienes are obtained from the reactions of cyclotrisilene c-Si3R4 (R = iPr3C6H2) with phenyl and diphenyl acetylene, respectively. With 1,4-diethynyl benzene the crossconjugated bridging of two of the Si3C2 cycles by a paraphenylene linker is achieved. UV/ vis spectroscopy indicates a small but significant effect of cross-conjugation, which is confirmed by TD-DFT calculations. The formation mechanism of the 1,2,3trisilacyclopentadienes is elucidated by VT NMR.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1132
https://doi.org/10.1039/c8cc03297a
ISSN: 1364-548X
Appears in Collections:JOURNAL ARTICLES

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