Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/66143
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dc.contributor.authorPanana Kitiphaisalnonten_US
dc.contributor.authorUpsorn Boonyangen_US
dc.contributor.authorJuttamanee Kowitthayaen_US
dc.contributor.authorSutatip Siripaisarnpipaten_US
dc.date.accessioned2019-08-21T09:18:22Z-
dc.date.available2019-08-21T09:18:22Z-
dc.date.issued2015en_US
dc.identifier.citationChiang Mai Journal of Science 42, 3 (July 2015), 712 - 717en_US
dc.identifier.issn0125-2526en_US
dc.identifier.urihttp://it.science.cmu.ac.th/ejournal/dl.php?journal_id=5956en_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/66143-
dc.description.abstractA reaction of a ligand 3,3´-(1,4-butanediyldinitrilo)bis(2-butanone)dioxime (BnH2) and CuCl yield green [Cu(H2dmg)Cl(μ-Cl)]2,1. The dimethylglyoxime (H2dmg) and CuIIions in 1 were in situ produced during the course of reaction and formed doubly chloro-bridged Cu(II) dimers. The geometry around copper ion is distorted square pyramidal. The weak intermolecular hydrogen bonds are observed in 1 giving 1D structure. The existence of two O–O distances of O2–O1= 2.922 Ǻ and O4–O3= 2.910 Ǻ indicates that these weak intermolecular hydrogen bonds are not equivalent. Hence doublet of the O-H stretching at 3302 and 3216 cm-1 are observed.en_US
dc.language.isoEngen_US
dc.publisherScience Faculty of Chiang Mai Universityen_US
dc.subjectdiiminedioximeen_US
dc.subjectcuprous chlorideen_US
dc.subjectdimethylglyoximeen_US
dc.subjecthydrogen bonden_US
dc.subjectdoubly chloro-bridged CuIIdimersen_US
dc.titleUnexpected Formation of Copper Dimethylglyoxime Dimer From the Reaction of Cuprous Chloride and Tetradentate Buthylene-Bridged Diiminedioxime Liganden_US
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