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dc.contributor.authorAygün , Muhittin
dc.contributor.authorÇetinkaya , Engin
dc.contributor.authorGök , Yetkin
dc.contributor.authorKendı ,Engin
dc.contributor.authorÇetinkaya , Bekir
dc.date.accessioned2019-12-13T06:35:43Z
dc.date.available2019-12-13T06:35:43Z
dc.date.issued2003
dc.identifier.issn0910-6340
dc.identifier.urihttps://doi.org/10.2116/analsci.19.1093
dc.identifier.urihttp://hdl.handle.net/11655/18597
dc.description.abstractIn the title compound, C23H32N4Se, was synthesized and its crystal structure was determined by single crystal X-ray diffraction. The compound crystallizes in orthorhombic system, space group Pbca, a = 10.9960(10)Angstrom, b = 14.9460(9)Angstrom, c = 27.565(5)Angstrom and Z = 2. According to X-ray crystallographic studies, the diazepine ring is observed to be in a disordered state. The site-occupancy of the major compenent refined to 0.53(1). The C=Se bond length of 1.862(4)Angstrom is a double bond character. The dihedral angle between the two phenyl rings is 37.7(2)degrees.
dc.language.isoen
dc.publisherJapan Soc Analytical Chemistry
dc.relation.isversionof10.2116/analsci.19.1093
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectChemistry
dc.titleSynthesis and Crystal Structure of Hexahydrobis[(1,3-P-Dimethylaminobenzyl)-1,3-Diazepinel]-2-Selenone, C23H32N4Setr_en
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalAnalytical Sciences
dc.contributor.departmentFizik Mühendisliği
dc.identifier.volume19
dc.identifier.issue7
dc.identifier.startpage1093
dc.identifier.endpage1094
dc.description.indexWoS
dc.description.indexScopus


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