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Synthesis and Pyrolytic Studies of Schiff Base Derivatives of Heterotrinucleic[AlIII-SnII-BIII]-µ-oxoisopropoxide

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1TitleTitle of DocumentSynthesis and Pyrolytic Studies of Schiff Base Derivatives of Heterotrinucleic[AlIII-SnII-BIII]-µ-oxoisopropoxide
2CreatorAuthor's name, affiliation, country RAJESH KUMAR
Department of Chemistry, Haryana Institute of Engineering & Technology, Kaithal-136027, Haryana, India
3SubjectDicipline(s) Chemical Science
3SubjectKeywords Heteronucleic-µ-oxoalkoxides, Aluminium, Tin, Boron, Schiff bases, TG analysis
4DescriptionAbstract New Schiff base derivatives of heteronucleic-µ-oxoisopropoxide[SnO2AlB(Opri)4] have been synthesized by thermal condensation of µ-oxoisopropoxide with salicylidene-aniline (HSB1), salicylidene-o-toluidene (HSB2), salicylidene-p-toluidene (HSB3) and salicylidene-p-chloroaniline (HSB4) in different molar ratios (1:1-1:2) yielded the compounds of the type [SnO2AlB(Opri)4-n (SB)n] (where n is 1-2 and SB = Schiff base anion). The Schiff base derivatives have been characterized by elemental, spectral (IR, 1H, 13C, 27Al, 119Sn and 11B NMR), thermal and molecular weight measurement. Hydrothermally assisted sol-gel process gives the hydrolyzed product and thermal study of these products favors the formation of multi-component oxides. The studies reveal that Schiff base derivatives are polymeric in nature and low susceptible to hydrolysis as compared to parent compound and may prove excellent precursors for the mixed metal oxides.
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  1 , Number  (2), (2012)
12LanuguageEnglish=en en
13RelationSupp.files
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