Electronic nature of zwitterionic alkali metal methanides, silanides and germanides – a combined experimental and computational approach
Author:
Affiliation:
1. Texas Tech University
2. Department of Chemistry and Biochemistry
3. Lubbock
4. USA
Abstract
Zwitterionic group 14 complexes of the alkali metals of formula [E(SiMe2OCH2CH2OMe)3M], where E = C, Si or Ge and M = Li, Na or K, have been prepared, structurally characterized and their electronic nature was investigated by computational methods.
Funder
National Science Foundation
Welch Foundation
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/SC/C6SC02390H
Reference109 articles.
1. Preparation and crystal structure of the novel internally solvated dimeric organolithium compound [{LiC(SiMe2OMe)3}2]
2. Synthesis, crystal structure and reactions of the dimeric organolithium compound [{[(MeO)Me2Si]3CLi}2]
3. Reaction of tris[(diphenylphosphino)dimethylsilyl]methane with molybdenum hexacarbonyl and deprotonation to give a salt with a planar carbanion. Crystal structures of (Ph2PMe2Si)3CH and [Li(tmen)2][C(SiMe2PPh2)3], tmen = N,N,N ′,N ′-tetramethylethane-1,2-diamine
4. Tris(triorganosilyl)methyl derivatives of potassium and lithium bearing dimethylamino or methoxy substituents at silicon. Crystal structures of KC(SiMe3)2(SiMe2NMe2), KC(SiMe2NMe2)3 and [LiC(SiMe3)(SiMe2OMe)2]2
5. Crowded organometallic compounds of the alkali metals with diphenylphosphino substituents in the organic group
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