Diisobutyl(phosphaneyl)alane: a simple PH2-transfer reagent for the synthesis of polyphosphaneyl compounds of silicon and germanium

Citation
M. Driess et C. Monse, Diisobutyl(phosphaneyl)alane: a simple PH2-transfer reagent for the synthesis of polyphosphaneyl compounds of silicon and germanium, Z ANORG A C, 626(5), 2000, pp. 1091-1094
Citations number
20
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE
ISSN journal
00442313 → ACNP
Volume
626
Issue
5
Year of publication
2000
Pages
1091 - 1094
Database
ISI
SICI code
0044-2313(200005)626:5<1091:DASPRF>2.0.ZU;2-7
Abstract
Introduction of PH3 into a solution of diisobutylaluminium hydride in hexan e furnishes, under evolution of H-2, the title compound [iBu(2)AlPH(2)](3) (4) The alane 4 is probably trimer in noncoordinating solvents such as hydr ocarbons and shows only a marginal tendency in such solutions to undergo di ssociation. A nucleophilic transfer of the PH2 group in 4 onto E-X-compound s of group 14 elements (E = Si, Ge; X = Cl) succeeds only in the presence o f THF which transforms 4 to the corresponding monomeric, THF-solvated alane 5. The latter is a remarkable mild phosphaneylation reagent, which facilit ates access to Si(PH2)(4) (1), Ge(PH2)(4) (2), MeSi(PH2)(3) (6), and EtSi(P H2)(3) (7) more efficiently.