Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9361
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dc.contributor.authorMathur, Pradeepen_US
dc.contributor.authorMobin, Shaikh M.en_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:32:33Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:32:33Z-
dc.date.issued2014-
dc.identifier.citationMathur, P., Tauqeer, M., Torubaev, Y. V., Shaikh, M. M., Lahiri, G. K., Pasynskii, A. A., & Pavlova, A. V. (2014). Step-by-step transformations of ferrocenyltellurium complexes of group VIB metal carbonyls. Journal of Organometallic Chemistry, 758, 55-59. doi:10.1016/j.jorganchem.2014.02.004en_US
dc.identifier.issn0022-328X-
dc.identifier.otherEID(2-s2.0-84896765538)-
dc.identifier.urihttps://doi.org/10.1016/j.jorganchem.2014.02.004-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9361-
dc.description.abstractStepwise interactions of photochemically generated M(CO)5(THF) (M = Cr, Mo, W) with diferrocenylditelluride initially generated mononuclear M(CO)5(Fc2Te2) followed by the bimetallic [M(CO)5]2(μ-Fc2Te2), with terminal and bridged Fc2Te2 moieties, respectively. On photolysis, [M(CO)5]2(μ-Fc2Te2) transformed to FcTe bridged and M-M bonded "butterfly" complexes [(CO)4M(μ-FcTe)]2 via the elimination of two carbonyl groups. The solid state structures and 125Te NMR spectral data of the new complexes and a new polymorphic form of Fc2Te2 having remarkable intermolecular Te⋯π-Cp short contacts (av. 3.5 Å) are discussed. © 2014 Elsevier B.V. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.sourceJournal of Organometallic Chemistryen_US
dc.subjectCarbonylationen_US
dc.subjectChemical bondsen_US
dc.subjectPhotolysisen_US
dc.subjectFerrocenylen_US
dc.subjectMetal carbonylen_US
dc.subjectMetal-metal bondsen_US
dc.subjectOrganotelluriumen_US
dc.subjectShort contactsen_US
dc.subjectMetalsen_US
dc.titleStep-by-step transformations of ferrocenyltellurium complexes of Group VIB metal carbonylsen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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