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Updated: May 28, 2026

A Protocol for Safe Lithiation Reactions Using Organolithium Reagents
Published on: November 12, 2016
Vinylgallium and alkyllithium compounds: transmetalation and generation of oligolithium cages
Werner Uhl1, Dirk Kovert, Marcus Layh
1Institut für Anorganische und Analytische Chemie der Universität Münster, Corrensstrasse 30, 48149 Münster, Germany. uhlw@uni-muenster.de
Abstract:
Vinylgallium compounds [C(6)H(6-n){(H)C=C(SiR(2) R')-GaR''(2)}(n ] (3, R=Ph, Me; R'=Ph, Me; R''=tBu, Et; n=1, 2) are easily accessible by hydrogallation of the corresponding alkynylbenzene derivatives with H-GaCl(2) and subsequent reaction with alkyllithium derivatives. Treatment of 3 with an excess amount of tert-butyl- or ethyllithium yielded by transmetalation and ortho-deprotonation of the aromatic rings the unprecedented solvent-free oligolithium cluster compounds [{(C(6)H(4)Li)HC=C(SiPh(3))Li}(2)(tBuLi)(2)] (4), [{(C(6)H(4)Li)HC=C(SiPh(2)Me)Li}(4)] (5) and [{(C(6)H(3)Li){HC=C(SiMe(3))Li}(2)}(3)] (6) in moderate yields. Their solid-state structures revealed the presence of unique molecular lithium clusters with 6, 8, or 9 lithium atoms that may be derived from two edge-sharing Li(4) tetrahedra (4), three Li(4) tetrahedra in a chain joined by two common edges (5) or a tricapped trigonal prism of lithium atoms (6).
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