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dc.contributor.authorIbis, Cemil
dc.contributor.authorTuyun, AMAÇ FATİH
dc.contributor.authorDeniz, NAHİDE GÜLŞAH
dc.date.accessioned2021-03-04T08:08:19Z
dc.date.available2021-03-04T08:08:19Z
dc.date.issued2010
dc.identifier.citationIbis C., Deniz N. G. , Tuyun A. F. , "Crystal Structure of 4-Bromo-3,4-Dichloro-1-(1-Morpholinyl)-1-(Decylsulfanyl)-2-Nitro-Buta-1,3-Diene", JOURNAL OF CHEMICAL CRYSTALLOGRAPHY, cilt.40, sa.4, ss.353-356, 2010
dc.identifier.issn1074-1542
dc.identifier.otherav_61c4f828-a95e-4c6a-9ed3-abe41ca0c787
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/68135
dc.identifier.urihttps://doi.org/10.1007/s10870-009-9660-7
dc.description.abstractThe compound 4-bromo-3,4-dichloro-1-(1-morpholinyl)-1-(decylsulfanyl)-2-nitro-buta-3-diene was synthesized from the reaction of 4-bromo-1,3,4-trichloro-1(decylsulfanyl)-2-nitro-buta-1,3-diene with morpholine and characterized by elemental analysis, IR spectrum, UV spectra, H-1 NMR, C-13 NMR and X-ray single crystal determination. In the title compound, C18H29BrCl2N2O3S, crystallizes in the monoclinic space group P2(1)/c, a = 15.8326(4) angstrom, b = 8.9915(10) angstrom, c = 16.7528(5) angstrom, beta = 100.808(10)degrees, V = 2,342.6(3) angstrom(3), Z = 4, R-1 = 0.0590 and wR(2) = 0.0940. The morpholine ring adopts a chair conformation. The morpholine ring and the butadiene group are inclined at an angle of 113.4 (1)degrees. The butadiene unit is not planar as can be expected if the two double bonds are fully conjugated.
dc.language.isoeng
dc.subjectSpektroskopi
dc.subjectTemel Bilimler
dc.subjectSıvı Kristaller ve Sıvı Kristal Polimerler
dc.subjectFizikokimya
dc.subjectSPEKTROSKOPİ
dc.subjectTemel Bilimler (SCI)
dc.subjectKimya
dc.subjectKRİSTALLOGRAFİ
dc.titleCrystal Structure of 4-Bromo-3,4-Dichloro-1-(1-Morpholinyl)-1-(Decylsulfanyl)-2-Nitro-Buta-1,3-Diene
dc.typeMakale
dc.relation.journalJOURNAL OF CHEMICAL CRYSTALLOGRAPHY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume40
dc.identifier.issue4
dc.identifier.startpage353
dc.identifier.endpage356
dc.contributor.firstauthorID80599


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