| Literature DB >> 26118362 |
Andrew J Keane1, Wesley S Farrell1, Brendan L Yonke1, Peter Y Zavalij1, Lawrence R Sita2.
Abstract
A highly efficient and versatile chemical cycle has been developed for the production of isocyanates through the molecular fixation of N2 , CO2 and R3 ECl (E=C, Si, and Ge). Key steps include a 'one-pot' photolytic N-N bond cleavage of a Group 6 dinuclear dinitrogen complex with in situ trapping by R3 ECl to provide a metal terminal imido complex that can engage in simultaneous nitrene-group transfer and oxygen-atom transfer to generate an intermediate metal terminal oxo complex with release of the isocyanate product. Reaction of the oxo complex with additional equivalents of R3 ECl regenerates a metal dichloride that is the precursor for dinuclear dinitrogen starting material.Entities:
Keywords: nitrene-group transfer; nitrogen fixation; oxygen-atom transfer; small-molecule activation
Year: 2015 PMID: 26118362 DOI: 10.1002/anie.201502293
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336