Please use this identifier to cite or link to this item: https://doi.org/10.1021/cg0499717
DC FieldValue
dc.titleIsomerism in 1D coordination polymers of Cu(II) complexes of N-(2-hydroxybenzyl)-L-valine: Influence of solvent and coordination sphere on the conformation
dc.contributor.authorYang, X.
dc.contributor.authorRanford, J.D.
dc.contributor.authorVittal, J.J.
dc.date.accessioned2014-10-16T08:48:20Z
dc.date.available2014-10-16T08:48:20Z
dc.date.issued2004-07
dc.identifier.citationYang, X., Ranford, J.D., Vittal, J.J. (2004-07). Isomerism in 1D coordination polymers of Cu(II) complexes of N-(2-hydroxybenzyl)-L-valine: Influence of solvent and coordination sphere on the conformation. Crystal Growth and Design 4 (4) : 781-788. ScholarBank@NUS Repository. https://doi.org/10.1021/cg0499717
dc.identifier.issn15287483
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/95478
dc.description.abstractThe reaction of the deprotonated N-(2-hydroxybenzyl)-L-valine ligand ("Sval") with Cu(II) salts afforded [Cu2(Sval) 2(H2O)3]n, 1, which has a 1D coordination polymeric structure cross-linked by strong hydrogen bonds to give 2D hydrogen-bonded coordination polymer in the solid state. Compound 1 can lose all the water molecules bonded to Cu(II) below 110°C. However, recrystallization from aqueous solution of anhydrous 1 gave a supramolecular isomer, [Cu2(Sval)2(H2O)]n· 2nH2O, 2. Interestingly, the thermal dehydration behavior of 2 is very similar to that of 1. Pseudo-supramolecular isomeric compounds of [Cu 2(Sval)2(H2O)n·0.5nC 3H7OH, 3, and [Cu4(SVal)4(H 2O)2(C4H9-OH)n· nC4H9OH, 4, were obtained when anhydrous 1 was recrystallized from 2-proponal and 1-butanol, respectively.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/cg0499717
dc.sourceScopus
dc.typeConference Paper
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/cg0499717
dc.description.sourcetitleCrystal Growth and Design
dc.description.volume4
dc.description.issue4
dc.description.page781-788
dc.identifier.isiut000222553800025
Appears in Collections:Staff Publications

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