Trimetallaborides as starting points for the syntheses of large metal-rich molecular borides and clusters.

ABSTRACT: Treatment of an anionic dimanganaborylene complex ([{Cp(CO)₂Mn}₂B]^-) with coinage metal cations stabilized by a very weakly coordinating Lewis base (SMe₂) led to the coordination of the incoming metal and subsequent displacement of dimethylsulfide in the formation of hexametalladiborides featuring planar four-membered M₂B₂ cores (M = Cu, Au) comparable to transition metal clusters constructed around four-membered rings composed solely of coinage metals. The analogies between compounds consisting of B₂M₂ units and M₄ (M = Cu, Au) units speak to the often overlooked metalloid nature of boron. Treatment of one of these compounds (M = Cu) with a Lewis-basic metal fragment (Pt(PCy₃)

SUBMITTER: Braunschweig H 

PROVIDER: S-EPMC5950574 | biostudies-literature | 2016 Jan

REPOSITORIES: biostudies-literature