Chemical Science Transactions | Chem Sci Trans | CST | Online Chemistry Journal | Open Access
Home | Table of Contents | Submit an article | Subscribe | Login | Register

Indexing Metadata

Synthesis, Structure and Characterization of Adducts of O-Propyldithiocarbonates with Substituted Pyridines

DUBLINCOREMETADATA ITEM METADATA FOR THIS DOCUMENT
1TitleTitle of DocumentSynthesis, Structure and Characterization of Adducts of O-Propyldithiocarbonates with Substituted Pyridines
2CreatorAuthor's name, affiliation, country INDERJEET KOUR*, GURPREET KOUR and RENU SACHAR
Department of Chemistry, University of Jammu, Jammu Tawi - 180006, India
3SubjectDicipline(s) Chemical Science
3SubjectKeywords Adducts, Xanthates (dithiocarbonates), Octahedrally coordinated, Direct methods, Crystal structure, π- π and C-H••• π interaction
4DescriptionAbstract A series of six coordinated Ni(II)complexes with general formula [Ni(C5H4NCl) 2 (S2COC3H7)2] was synthesized and characterized. All the complexes have 1:2 stoichiometry, are non ionic and paramagnetic in nature. TGA-DTA studies show the formation of NiS as the stable end product of the decomposition. One of the adducts bis(O-propyldithiocarbonato)bis (3-chloropyridine) nickel(II) crystallizes in the monoclinic space group P21/c. The Ni2+ ion is in an octahedral coordination environment formed by an N2S4 donor set, defined by two chelating dithiocarbonate anions as well as two 3-chloropyridine ligands with the Ni2+ ion located at the inversion centre. The packing of layers of molecules is stabilized by weak π - π and C-H•••π interactions. The asymmetric unit comprises of half molecule and Nickel(II) cation lies on an inversion centre
5PublishersOrganizing agency, location WWW Publications, India
6Contributor Sponsor(s) -
7DateDate (YYYY-MM-DD) -
8TypeStatus & genre Peer-reviewed Article
8TypeType
9FormateFile Formate PDF
10IdentifierUniform Resource Identifier Click Here
10IdentifierDigital Object Identifier
11SourceJournal/conference title; vol., no. (Year)Chemical Science Transactions, Volume  3 , Number  (3), (2014)
12LanuguageEnglish=en en
13RelationSupp.files
14Coverage -
15CopyrightCopyright and permissions
Chemical Science Transactions | Chem Sci Trans | CST | Online Chemistry Journal | Open Access
Home | Table of Contents | Submit an article | Subscribe | Login | Register