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Please use this identifier to cite or link to this item: http://repository.iitr.ac.in/handle/123456789/3692
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dc.contributor.authorNath, Mala-
dc.contributor.authorSharma N.-
dc.contributor.authorSharma C.L.-
dc.date.accessioned2020-10-06T14:28:03Z-
dc.date.available2020-10-06T14:28:03Z-
dc.date.issued1990-
dc.identifier.citationSynthesis and Reactivity in Inorganic and Metal-Organic Chemistry(1990), 20(5): 623-643-
dc.identifier.issn945714-
dc.identifier.urihttps://doi.org/10.1080/00945719008048160-
dc.identifier.urihttp://repository.iitr.ac.in/handle/123456789/3692-
dc.description.abstractFive coordinated complexes of di- and triphenyltin (IV) moieties with semi- and thiosemicarbazones of furfuraldehyde, 2-methoxybenzaldehyde, 4-methoxybenzaldehyde, benzylmethylketone, benzil, salicylaldehyde, o-hydroxynaphthaldehyde and o-hydroxyacetophenone in 1:1 molar ratio have been synthesized and characterized on the basis of elemental analyses, conductance measurements, electronic, IR, Far IR, 1HNMR and mossbauer spectral studies. The non-electrolytic complexes are proposed to have distorted trigonal bipyramidal geometry around tin atoms with two equatorial and one axial phenyl groups in the triphenyltin complexes and with two axial phenyl groups in the diorganotin complexes. The ligands are coordinated through N and 0 or S and ONO or ONS donar sites. © 1990, Taylor & Francis Group, LLC. All rights reserved.-
dc.language.isoen_US-
dc.relation.ispartofSynthesis and Reactivity in Inorganic and Metal-Organic Chemistry-
dc.titleDi- and triphenyltin (iv) complexes of semi- and thiosemicarbazones-
dc.typeArticle-
dc.scopusid7103033909-
dc.scopusid57205972230-
dc.scopusid7202115093-
dc.affiliationNath, M., Department of Chemistry, University of Roorkee, ROORKEE, 247 667, India-
dc.affiliationSharma, N., Department of Chemistry, University of Roorkee, ROORKEE, 247 667, India-
dc.affiliationSharma, C.L., Department of Chemistry, University of Roorkee, ROORKEE, 247 667, India-
dc.description.fundingThe authors are highly thankful to the Head of the Chemistry Department, U .O .R . , Roorkee , for providing laboratory facilities. Thanks are also due to Prof. R.P. Ghandhi (I.I.T, New Delhi) for ‘HNMR spectra and to Dr. A.K. Singh (I,I.T., New Delhi) for microanalyses and far 1.K. spectra and Dr. Bhargava (B.A.R.C., Bombay) for recording the M6ssbauer spectra of one compound. One of the authors (N.S.) gratefully acknowledges U.P.C.S.T., Lucknow, for awarding a Junior Research Fellowship.-
Appears in Collections:Journal Publications [CY]

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