Abstract

The reaction of [CpMo(CO)3]2 with dicyclopentamethylenethiuram disulfide in refluxing xylene resulted a novel mono nuclear complex, cis-[(CpMo(CO)2{S2C-N(CH2)5}] as red crystals in moderate yield. The compound was formed by the oxidative cleavage of metal-metal bond in [CpMo(CO)3]2 together with a reductive sulfur-sulfur bond scission in the ligand.

Highlights

  • Dicyclopentamethylenethiuram Disulfide (Dcpmtd), Oxidation Number, Oxidative Cleavage, Coordination Number, Mononuclear Complex, X-Ray Crystal Structure

  • The compound is formed by oxidative cleavage of Mo-Mo triple bond together with a reductive S-S bond scission in tetramethylthiuram disulfide ligand (Scheme 1)

  • We carried out the analogous reaction of dicyclopentamethylenethiuram disulfide with [CpMo(CO)3]2 and reported the formation of a mononuclear cyclopentadienyl molybdenum dicarbonyl complex, cis-[(CpMo(CO)2{S2C-N(CH2)5}]

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Summary

Introduction

Dicyclopentamethylenethiuram Disulfide (Dcpmtd), Oxidation Number, Oxidative Cleavage, Coordination Number, Mononuclear Complex, X-Ray Crystal Structure Scientific Research Publishing Inc. This work is licensed under the Creative Commons Attribution International Http://creativecommons.org/licenses/by/4.0/ Dithiocarbamate ligands are versatile ligands with applications in industry [1], agri- Since these ligands contain nitrogen and sulfur donor atoms, they are capable of forming complexes with most of the elements [4].

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