Please use this identifier to cite or link to this item: https://repository.cihe.edu.hk/jspui/handle/cihe/1715
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dc.contributor.authorBligh, Annie Sim Wanen_US
dc.contributor.otherPatil, B. R.-
dc.contributor.otherMachakanur, S. S.-
dc.contributor.otherBadiger, D. S.-
dc.contributor.otherHunoor, R. S.-
dc.contributor.otherGudasi, K. B.-
dc.contributor.otherNethaji, M.-
dc.date.accessioned2021-11-12T06:49:25Z-
dc.date.available2021-11-12T06:49:25Z-
dc.date.issued2011-
dc.identifier.urihttps://repository.cihe.edu.hk/jspui/handle/cihe/1715-
dc.description.abstractA series of novel hexasubstituted cyclophosphazene hydrazones [N<sub>3</sub>P<sub>3</sub>(—OC<sub>6</sub>H<sub>4</sub>—p—CH═N—NH—C(O)—C<sub>6</sub>H<sub>4</sub>—p—X)<sub>6</sub>] (X = H, Br, Cl, F, OH, OCH<sub>3</sub>, CH<sub>3</sub>, NO<sub>2</sub>, NH<sub>2</sub>) were prepared by a sixfold condensation reaction of [N<sub>3</sub>P<sub>3</sub>(—OC<sub>6</sub>H<sub>4</sub>—p—CHO)<sub>6</sub>] with para-substituted benzoic hydrazides [NH2—NH—C(O)—C<sub>6</sub>H<sub>4</sub>—p—X] with excellent yields (91–98%). The structures of the compounds were confirmed by elemental analysis, FT-IR, <sup>1</sup>H, <sup>13</sup>C, <sup>31</sup>P, 2D-HSQC NMR and mass spectrometry (MALDI-TOF). All the synthesized cyclophosphazene hydrazones exhibit high thermal stability. The crystal structure of a homogeneously substituted hexakis(4-formylphenoxy)-cyclotriphosphazene was determined by X-ray diffraction analysis. The compound crystallizes in the monoclinic system, space group P2<sub>1</sub>/n with a = 16.558(3) Å, b = 10.250(2) Å, c = 23.429(5) Å, α = γ = 90.00°, β = 90.461(4)°, V = 3976.5(14) Å<sup>3</sup> and Z = 4. The R value is 0.0823 for 4290 observed reflections. The conformations of the 4-formylphenoxy-groups are different at the three phosphorus atoms.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofJournal of Molecular Structureen_US
dc.titleHexa-arm star shaped hydrazone derivatives from hexakis(4-formylphenoxy)-cyclotriphosphazene coreen_US
dc.typejournal articleen_US
dc.identifier.doi10.1016/j.molstruc.2011.07.020-
dc.contributor.affiliationSchool of Health Sciencesen_US
dc.relation.issn0022-2860en_US
dc.description.volume1003en_US
dc.description.issue1-3en_US
dc.description.startpage52en_US
dc.description.endpage61en_US
dc.cihe.affiliatedNo-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.cerifentitytypePublications-
item.openairetypejournal article-
item.languageiso639-1en-
crisitem.author.deptS.K. Yee School of Health Sciences-
crisitem.author.orcid0000-0002-4757-2159-
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