Reactivity of distibanes toward trialkylalanes and -gallanes: Syntheses and X-ray structures of bisadducts and heterocycles

Citation
A. Kuczkowski et al., Reactivity of distibanes toward trialkylalanes and -gallanes: Syntheses and X-ray structures of bisadducts and heterocycles, ORGANOMETAL, 20(10), 2001, pp. 2000-2006
Citations number
42
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANOMETALLICS
ISSN journal
02767333 → ACNP
Volume
20
Issue
10
Year of publication
2001
Pages
2000 - 2006
Database
ISI
SICI code
0276-7333(20010514)20:10<2000:RODTTA>2.0.ZU;2-P
Abstract
Reactions between distibanes of the type Sb2R4 and trialkylalanes and -gall anes R ' M-3 in 1:2 stoichiometry yield eight bisadducts of the type [Sb2R4 ] [MR ' (3)](2) (R = Me, R ' = t-Bu, M = Al 1, Ga 2; R = Et, M = Al, R ' = Me 3, Et 4, t-Bu 5; M = Ga, R ' = Me 6, Et 7, t-Bu 8), which were character ized by multinuclear NMR studies and elemental analysis. In addition, 1, 2, 5, and 8 are the first structurally characterized neutral main group Lewis acid-distibane bisadducts. 1-8 are unstable in solution toward the formati on of heterocycles of the type [R2SbMR ' (2)](x). [Me2SbGa(t-Bu)(2)](3) (9) and [Et2SbGa(t-Bu)(2)](2) (10) have been isolated and their solid state st ructures determined by single-crystal X-ray diffraction.