Abstract

Abstract The oxidative addition reactions of selenocyanogen with [M(P(C6H5)3)4] (M [dbnd] Pd, Pt) in ethyl ether: pentane:ethanol (5:5:2 by volume) at −78°C under nitrogen lead to the formation of the complexes trans-[M(P(C6H5)3)2 (SeCN)2]. Although the selenocyanates are Se-bound in both complexes in the solid state, dissolution of the Pt(II) complex in methylene chloride or DMF leads to partial isomerization to the N-bonded form.

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