Abstract

The cone angle of the phosphine ligands in the heteronuclear cluster compounds [Cu2Ru4(µ3-H)2(CO)12(PR3)2](R = alkyl or aryl) has a marked effect on the metal framework structure adopted; when R = CHMe2, two skeletal isomers, which interconvert at ambient temperature, are present in solution and when R = cyclo-C6H11, the cluster exhibits a previously unobserved type of Cu2Ru4 metal core structure.

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