Can Remote N‐Heterocyclic Carbenes Coordinate with Main Group Elements? Synthesis, Structure, and Quantum Chemical Analysis of N+‐Centered Complexes

dc.contributor.authorMandal, S.K.
dc.date.accessioned2020-11-23T08:56:13Z
dc.date.available2020-11-23T08:56:13Z
dc.date.issued2018
dc.descriptionOnly IISERM authors are available in the record.
dc.description.abstractRemote N-heterocyclic carbenes (rNHCs), such as N-methyl-4-pyridylidene, are known to form coordination complexes with TMs. Herein, it is established that rNHCs can also coordinate to the N+ centre. Synthesis of some novel divalent NI complexes with the general formula (rNHC)→N+←(NHC) and (rNHC)→N+←(rNHC) was achieved, and X-ray diffraction studies supported the coordination bond character between the rNHCs and the N+ centre. Quantum chemical analysis established the presence of divalent NI character at the central nitrogen in these systemsen_US
dc.identifier.citationChemistry - A European Journal, 24(24), pp. 6418-6425en_US
dc.identifier.otherhttps://doi.org/10.1002/chem.201705999
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.201705999
dc.identifier.urihttp://hdl.handle.net/123456789/2050
dc.language.isoenen_US
dc.publisherWiley-VCH Verlagen_US
dc.subjectCarbene ligandsen_US
dc.subjectDivalent NI compoundsen_US
dc.subjectDonor–acceptor systemsen_US
dc.subjectQuantum chemical analysisen_US
dc.titleCan Remote N‐Heterocyclic Carbenes Coordinate with Main Group Elements? Synthesis, Structure, and Quantum Chemical Analysis of N+‐Centered Complexesen_US
dc.typeArticleen_US

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