Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/42796
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dc.contributor.authorSarkar, Rupa-
dc.contributor.authorSinha, Debopam-
dc.contributor.authorMaity, Amit-
dc.contributor.authorRajak, Kajal Krishna-
dc.date.accessioned2017-09-19T05:52:56Z-
dc.date.available2017-09-19T05:52:56Z-
dc.date.issued2017-09-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/42796-
dc.description913-924en_US
dc.description.abstractThe red colored mononuclear rhenium(I) complex having fac-[Re(CO)3]+ moiety of general formula, [Re(CO)3(NN)Cl], has been synthesized in excellent yield by reacting [Re(CO)5Cl] with 2-(benzothiazol-2-yl) quinoline (1:1) in a boiling mixture of methanol+chloroform (3:1, v/v) under argon atmosphere. Elemental, 1H and 13C NMR analysis show the formation of the desired complex. The complex is also characterized by different spectroscopic techniques. The ground and excited-state geometries, NMR, absorption, and phosphorescence properties of the Re(I) complex are examined by DFT and TDDFT methods. The natural transition orbital and spin density difference map analysis reveals the nature of excitations. The lowest lying triplet excited state is associated with the 3MLCT/3ILCT excited state. The emission-like transition is consistent with the strong 3MLCT/ 3ILCT character.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.56A(09) [September 2017]en_US
dc.subjectCoordination chemistryen_US
dc.subjectDensity functional calculationsen_US
dc.subjectPhosphorescenceen_US
dc.subjectPhotophysical propertiesen_US
dc.subject3MLCT excited stateen_US
dc.subjectNatural transition orbitalsen_US
dc.subjectElectrochemical studiesen_US
dc.subjectQuinoline nitrogenen_US
dc.subjectRheniumen_US
dc.titleRhenium(I) complex with 2-(benzothiazol-2-yl) quinoline: Synthesis, characterization, spectral properties and DFT/TDDFT investigationsen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.56A(09) [September 2017]

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