Please use this identifier to cite or link to this item: doi:10.22028/D291-37851
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Title: Phenylene-bridged cross-conjugated 1,2,3-trisilacyclopentadienes
Author(s): Zhao, Hui
Klemmer, Lukas
Cowley, Michael J.
Majumdar, Moumita
Huch, Volker
Zimmer, Michael
Scheschkewitz, David
Language: English
Title: Chemical Communications
Volume: 54
Issue: 60
Pages: 8399-8402
Publisher/Platform: Royal Society of Chemistry
Year of Publication: 2018
DDC notations: 500 Science
Publikation type: Journal Article
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 cross-conjugated bridging of two of the Si3C2 cycles by a para-phenylene 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 1,2,3-trisilacyclopentadienes is elucidated by VT NMR.
DOI of the first publication: 10.1039/c8cc03297a
URL of the first publication: https://pubs.rsc.org/en/content/articlelanding/2018/cc/c8cc03297a
Link to this record: urn:nbn:de:bsz:291--ds-378511
hdl:20.500.11880/34231
http://dx.doi.org/10.22028/D291-37851
Date of registration: 7-Nov-2022
Description of the related object: Supplementary files
Related object: https://www.rsc.org/suppdata/c8/cc/c8cc03297a/c8cc03297a1.pdf
Faculty: NT - Naturwissenschaftlich- Technische Fakultät
Department: NT - Chemie
Professorship: NT - Prof. Dr. David Scheschkewitz
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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