z-logo
Premium
Synthese, NMR‐Spektren und Molekülstruktur von [(CH 3 ) 2 Ga{μ‐P(H)Si(CH 3 ) 3 } 2 Ga(CH 3 ) 2 {μ‐P(Si(CH 3 ) 3 ) 2 }Ga(CH 3 ) 2 ]
Author(s) -
Schaller A.,
Hausen † H.D.,
Weidlein J.,
Fischer P.
Publication year - 2000
Publication title -
zeitschrift für anorganische und allgemeine chemie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.354
H-Index - 66
eISSN - 1521-3749
pISSN - 0044-2313
DOI - 10.1002/(sici)1521-3749(200003)626:3<616::aid-zaac616>3.0.co;2-4
Subject(s) - monoclinic crystal system , toluene , chemistry , crystallography , yield (engineering) , nmr spectra database , stereochemistry , crystallization , crystal structure , ring (chemistry) , nuclear magnetic resonance spectroscopy , spectral line , materials science , organic chemistry , physics , astronomy , metallurgy
Synthesis, NMR Spectra and Structure of [(CH 3 ) 2 Ga{μ‐P(H)Si(CH 3 ) 3 } 2 Ga(CH 3 ) 2 {μ‐P(Si(CH 3 ) 3 ) 2 }Ga(CH 3 ) 2 ] The title compound has been prepared in good yield by the reaction of [Me 2 GaOMe] 3 (Me = CH 3 ) with HP(SiMe 3 ) 2 in toluene (ratio 1 : 1,1) and purified by crystallization from pentane or toluene, respectively. This organogallium compound forms (Ga–P) 3 ring skeletons with one Ga–P(SiMe 3 ) 2 –Ga and two Ga–P(H)SiMe 3 –Ga bridges and crystallizes in the monoclinic space group C2/c. The known homologous Al‐compound is isotypic, both (M III –P) 3 heterocycles have twist‐conformations, the ligands of the monophosphane bridges have trans arrangements.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom