Reduction of Terphenyltrifluorosilanes: C−C Insertion Products and Possible Formation of a Disilyne
Author:
Affiliation:
1. Lehrstuhl für Anorganische Chemie I, Ruhr-Universität-Bochum, Universitätsstrasse 150, D-44780 Bochum, Germany
2. Department of Chemistry, University of WisconsinMadison, 1101 University Avenue, Madison, Wisconsin 53706
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om990924z
Reference22 articles.
1. Element Derivatives of Sterically Encumbering Terphenyl Ligands
2. Synthesis and Characterization of [Sn2{C6H3-2,6(2,4,6-i-Pr3C6H2)2}2]-•: A Singly Reduced Valence Isomer of a “Distannyne”
3. Reduction of Ge(Cl)C6H3mes2-2,6 to give the cyclotrigermenyl radical (GeC6H3mes2-2,6)3· and the trigermenyl anion salt K(GeC6H3mes2-2,6)3
4. The Syntheses and Characterization of the Bulky Terphenyl Silanes and Chlorosilanes 2,6-Mes2C6H3SiCl3, 2,6-Trip2C6H3SiCl3, 2,6-Mes2C6H3SiHCl2, 2,6-Trip2C6H3SiHCl2, 2,6-Mes2C6H3SiH3, 2,6-Trip2C6H3SiH3and 2,6-Mes2C6H3SiCl2SiCl3
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