
Journal of Organometallic Chemistry p. C1 - C5 (1985)
Update date:2022-08-02
Topics:
Colbran, Stephen B.
Johnson, Brian F. G.
Lewis, Jack
Sorrell, Robert M.
Phosphine-substituted triosmium clusters Os3(CO)11PR1R2H (a: R1=R2=H; b: R1=Ph, R2=H; c: R1,R2=Ph) have been found to yield, via a deprotonation/protonation sequence, the phosphido-bridged clusters (μ-H)Os3(CO)10-(μ-PR1R2): the intermediate anions <(Os3(CO)10(μ-PR1R2))-> and <((μ-H)Os3(CO)10(μPR1))-> in this systematic synthesis are described.
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