Chemistry of low-valent molybdenum phosphite complexes: Models of seven-coordinate reaction intermediates

Abstract

A simple synthesis of the zerovalent complex Mo[P(OCH(3))(3)](6) has been devised from a potassium reduction of MoCl(4)(tetrahydrofuran)(2) followed by reaction with trimethyl phosphite at 70 degrees . Protonation of this octahedral complex gave only low yields of the expected seven-coordinate hydride, HMo[P(OCH(3))(3)](6) (+). The major product was an octahedral nonhydridic cation, Mo[P(OCH(3))(3)](5)P(OCH(3))(2) (+), derived from proton cleavage of the P-O phosphite ester bond. This octahedral cation was stereochemically nonrigid, apparently through facile methoxy group migration. Close packing by methoxy groups in this fluxional cation was established through an x-ray crystallographic study of Mo[P(OCH(3))(3)](5)P(OCH(3))(2) (+)-PF(6) (-). Extended reaction of trifluoroactic acid with Mo[P(OCH(3))(3)](6) yielded the seven-coordinate hydride, HMo[P(OCH(3))(3)](4)(O(2)CCF(3)), which was near pentagonal bipyramidal and was stereochemically nonrigid.