Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2498
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dc.contributor.authorKhullar, S.-
dc.contributor.authorGupta, Vijay-
dc.contributor.authorMandal, S.K.-
dc.date.accessioned2020-12-02T08:44:01Z-
dc.date.available2020-12-02T08:44:01Z-
dc.date.issued2016-
dc.identifier.citationChemistry - A European Journal, 22(3), pp. 1088-1096en_US
dc.identifier.otherhttps://doi.org/10.1002/chem.201503618-
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/chem.201503618-
dc.identifier.urihttp://hdl.handle.net/123456789/2498-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractThe dative‐bond representation (L→E) in compounds with main group elements (E) has triggered extensive debate in the recent past. The scope and limits of this nonclassical coordination bond warrant comprehensive exploration. Particularly compounds with (L→N←L′)+ arrangement are of special interest because of their therapeutic importance. This work reports the design and synthesis of novel chemical species with the general structural formula (L→N←L′)+ carrying the unusual ligand cyclohexa‐2,5‐diene‐4‐(diaminomethynyl)‐1‐ylidene. Four species belonging to the (L→N←L′)+ class carrying this unconventional ligand were synthesized. Quantum chemical and X‐ray diffraction analyses showed that the electronic and geometric parameters are consistent with those of already reported divalent NI compounds. The molecular orbital analysis, geometric parameters, and spectral data clearly support the L→N and N←L′ interactions in these species. The newly identified ligand has the properties of a reactive carbene and high nucleophilicity.en_US
dc.language.isoenen_US
dc.publisherWiley-VCH Verlagen_US
dc.subjectCarbene ligandsen_US
dc.subjectDensity functional calculationsen_US
dc.subjectLigand designen_US
dc.subjectNitrogenen_US
dc.titleDesign, Synthesis, and Structural Analysis of Divalent NI Compounds and Identification of a New Electron‐Donating Liganden_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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