ISSN:
0009-2940
Schlagwort(e):
Silylgallanes
;
Gallium compounds
;
Hydroxygallium compounds
;
Gallium alkoxides
;
Chemistry
;
Inorganic Chemistry
Quelle:
Wiley InterScience Backfile Collection 1832-2000
Thema:
Chemie und Pharmazie
Notizen:
Reaction of lithium tris(trimethylsilyl)silanide · 3 THF with R2GaCl (R = 2,2,6,6-tetramethylpiperidino, Me, Cl) yields tmp2GaSi(SiMe3)3 (3) and R2Ga(THF)Si(SiMe3)3 (R = Me, Cl) (7, 9). Both gallium nitrogen bonds in 3 are cleaved by protic reagents. Depending on the acidity of these agents, either oligomeric gallanes [(RO)2GaSi(SiMe3)3]n (R = Et, H, n = 2, 3) (11, 12) or tetramethylpiperidinium gallates [X3GaSi-(SiMe3)3]- (X = OPh, Cl) (13, 14) are formed. Hydroxide 11 adds lithium hydroxide to afford the mixed lithium gallium hydroxide 15. Single-crystal X-ray diffraction studies confirm the suggested constitutions. The gallium-silicon bond can adopt values between 236 and 247 pm. Here electronic influences of the substituents on the gallium center are of great importance as well as their steric demand. This is underlined by quantum chemical calculations on the ab initio (SCF) level.
Zusätzliches Material:
7 Ill.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1002/cber.19961290514
Permalink