Synthesis, Characterization, and Electrochemical Properties of Bisosmabenzenes Bridged by Diisocyanides.

Treatment of osmabenzene [Os(CHC(PPh3)CHC(PPh3)CH)Cl2(PPh3)2]OH (3) with various diisocyanides in the presence of NH4PF6afforded a series of diisocyanide-bridged bisosmabenzenes [(μ-CN−R−NC){Os(CHC(PPh3)CHC(PPh3)CH)Cl2(PPh3)}2][PF6]2(R = 4,4′-C6H4-C6H4(5a), 4,4′-C6H4CH2C6H4(5b), 4,4′-C6H4OC6H4(5c), 1,4-C6H4(5d)) in good yields through ligand substitution reactions. Similarly, reaction of osmafuran [Os(CHC(PPh3)C(OEt)O)Cl2(PPh3)2] (6) with 1,4-phenylenediisocyanide produced the diisocynide-bridged bisosmafuran [μ-(1,4-phenylenediisocyanide){Os(CHC(PPh3)C(OEt)O)Cl(PPh3)2}2]Cl2(7). Bisosmabenzenes containing a chloro and a phosphonium substituent on each metallacycle [(μ-CN−R−NC){Os(CHC(PPh3)CHCClCH)Cl(PPh3)2}2]Cl2(R = 4,4′-C6H4-C6H4(9a), 4,4′-C6H4CH2C6H4(9b), 4,4′-C6H4OC6H4(9c), 1,4-C6H4(9d)) could be obtained in modest yields from the reactions of the osmacycle [Os(CHC(PPh3)CH(OH)-η2-CCH)Cl2(PPh3)2] (8) with corresponding diisocyanides in the presence of NH4PF6and NaCl via nucleophilic addition reactions. All of these complexes have been fully characterized by 1H, 31P{1H}, and 13C{1H} NMR spectrometry, IR spectrometry, and elemental analyses. Moreover, the structure of 9dhas been established by X-ray crystallography. The electrochemical properties of stable bisosmabenzenes 9a−dhave been investigated, which revealed that the two metal centers in 9cand 9dcan interact with each other through a diisocyanide bridge. [ABSTRACT FROM AUTHOR]