Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4444
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dc.contributor.authorMAURYA, DEVESHen_US
dc.contributor.authorKarmakar, Joyen_US
dc.contributor.authorSAHOO, PADMINIen_US
dc.contributor.authorRAUT, RAVINDRA K.en_US
dc.contributor.authorMAJUMDAR, MOUMITAen_US
dc.date.accessioned2020-02-26T06:33:36Z
dc.date.available2020-02-26T06:33:36Z
dc.date.issued2020-04en_US
dc.identifier.citationInorganica Chimica Acta, 503.en_US
dc.identifier.issn0020-1693en_US
dc.identifier.issn1873-3255en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4444-
dc.identifier.urihttps://doi.org/10.1016/j.ica.2019.119380en_US
dc.description.abstractThe compliance of three acyclic flexible ligands of the type N2X2 with CH2CH2 linker in the backbone: diiminodi(furan) L1, diiminodi(thiophene) L2 and diiminodiphosphine L3 have been employed for the coordination of chlorogermyliumylidene and gold(I) chloride units. The chlorogermyliumylidenes have been stabilized by the two imino nitrogen coordinating sites present in L1 and L2 yielding compounds 1 and 2 respectively. Based on metal:ligand stoichiometry used, the phosphino groups present in L3 can coordinate to either one AuCl unit giving compound 3 or to two AuCl units forming compound 4. All the compounds have been characterized by NMR techniques and single crystal X-ray crystallography.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectChlorogermyliumylideneen_US
dc.subjectAmbiphilicen_US
dc.subjectElectronic stabilizationen_US
dc.subjectTetradentate liganden_US
dc.subjectGold(I)en_US
dc.subjectTOC-FEB-2020en_US
dc.subject2020en_US
dc.titleVersatile binding modes of acyclic N2X2 (X = O, S and P) ligands towards [GeCl]+ and AuCl unitsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleInorganica Chimica Actaen_US
dc.publication.originofpublisherForeignen_US
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