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dc.contributor.authorGuo, Dan Danen
dc.contributor.authorWang, Dunen
dc.contributor.authorFan, Zhi Jinen
dc.contributor.authorLi, Juan Juanen
dc.contributor.authorSong, Hai Binen
dc.contributor.authorFan, Qianen
dc.contributor.authorKalinina, Tatiana A.en
dc.contributor.authorMorzherin, Y. Y.en
dc.contributor.authorBelskaya, N. P.en
dc.contributor.authorBakulev, V. A.en
dc.date.accessioned2017-09-04T14:45:45Z-
dc.date.available2017-09-04T14:45:45Z-
dc.date.issued2012-
dc.identifier.citationSynthesis, X-ray structure and bioactivity of N-4-methyl-1,2,3-thiadiazole- 5-carbonyl-N'-3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxyl)phenyl urea / Dan Dan Guo, Dun Wang, Zhi Jin Fan, Juan Juan Li, Hai Bin Song, Qian Fan, Tatiana A. Kalinina, Y. Y. Morzherin, N. P. Belskaya, V. A. Bakulev // Jiegou Huaxue. — 2012. — Vol. 31. — № 12. — P. 1721-1728.en
dc.identifier.issn0254-5861-
dc.identifier.other3good_DOI
dc.identifier.other0ea3e63b-c1ff-4b6b-91b8-12c4b3690255pure_uuid
dc.identifier.otherhttp://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=84870941837m
dc.identifier.urihttp://elar.urfu.ru/handle/10995/51344-
dc.description.abstractThe title compound N-4-methyl-1,2,3-thiadiazole-5-carbonyl-N'-3,5-dichloro- 4- (1,1,2,2- tetrafluoroethoxyl)phenyl urea (C13H8Cl 2F4N4O3S, Mr = 447.19) has been synthesized from 4-methyl- 1,2,3-thiadiazole-5-carbonyl chloride as the starting material, and its structure was characterized by proton Nuclear Magnetic Resonance (1H NMR), Infra Red Spectroscopy (IR), high-resolution mass spectroscopy (HRMS), and single-crystal X-ray diffraction. The crystal of the title compound belongs to triclinic, space group P1 with a = 6.0780(8), b = 11.3760(14), c = 12.1440(18) Å, α = 96.887(7), β = 91.027(12), γ = 104.252(13)°, Z = 2, V = 806.98(19) Å3, Dc = 1.840 g/cm3, μ = 0.601 mm-1, F(000) = 448, R = 0.0450 and wR = 0.0869. X-ray analysis indicates that the 1,2,3-thiadiazole ring is not coplanar with the phenyl ring, and the dihedral angle is 33.57°. Two intermolecular hydrogen bonds N(2)-H···O(1), S(1)·H-C(11), and three weak intermolecular interactions, C(11) ·O(1), N(1) ·O(2) and S·O(1), are observed. The bioassay results indicate that the title compound has good insecticidal activity against Culex pipiens pallens and good induction activity for tobacco against tobacco mosaic virus which is equal to that of TDL.en
dc.language.isoenen
dc.sourceJiegou Huaxueen
dc.subject1,2,3-THIADIAZOLEen
dc.subjectBIOLOGICAL ACTIVITYen
dc.subjectCRYSTAL STRUCTUREen
dc.subjectSYNTHESISen
dc.titleSynthesis, X-ray structure and bioactivity of N-4-methyl-1,2,3-thiadiazole- 5-carbonyl-N'-3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxyl)phenyl ureaen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.typeinfo:eu-repo/semantics/articleen
dc.identifier.scopus84870941837-
local.affiliationState Key Laboratory of Elemento Organic Chemistry, Nankai University, Tianjin 300071, Chinaen
local.affiliationSichuan Functional Heterocyclic Compounds Engineering Technology Research Center, Lier Chemicals Co., Ltd., No.97 Mianxingdonglu, Mianyang, Sichuan 621000, Chinaen
local.affiliationUral Federal University Named after the First President of Russia B. N. Yeltsin, Yeltsin UrFU, 620002, Ekaterinburg, Russian Federationen
local.contributor.employeeКалинина Татьяна Андреевнаru
local.contributor.employeeМоржерин Юрий Юрьевичru
local.contributor.employeeБельская Наталия Павловнаru
local.contributor.employeeБакулев Василий Алексеевичru
local.description.firstpage1721-
local.description.lastpage1728-
local.issue12-
local.volume31-
dc.identifier.wos000313530200005-
local.contributor.departmentХимико-технологический институтru
local.identifier.pure1071188-
local.identifier.eid2-s2.0-84870941837-
local.identifier.wosWOS:000313530200005-
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