Abstract
A mechanism for conversion of thiols into disulfides and dihydrogen catalyzed by CpMn(CO)3 was studied in detail with the aid of density functional theory computations. Four major steps are involved in both of the two possible pathways (path1 and path2): (1) a ligand substitution process (dissociation of one carbonyl ligand and subsequent addition of RSH to the metal center); (2) intermolecular hydride migration; (3) addition of RSH and release of dihydrogen; (4) production of S2R2 and regeneration of the catalyst. Migration of the hydrogen from RSH to Cp ring can not be completed in one step, but need to form the key intermediate CpMnH(CO)2SR first. Ligand substitution process is the rate-determined reaction step. Path1 is the dominant pathway compared with path2, which mainly results from difficult formation of the five-member transition state in path2.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
