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首页> 外文期刊>Acta Chimica Slovenica >The Synthesis of Novel 5-, 5,5-, 5,5,5-, S,O-, N,S-Substituted Halogenobuta-1,3-dienes
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The Synthesis of Novel 5-, 5,5-, 5,5,5-, S,O-, N,S-Substituted Halogenobuta-1,3-dienes

机译:新型5、5、5、5、5、5、5-,S,O-,N,S取代的Halobobuta-1,3-dienes的合成

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摘要

In this work, thiosubstituted nitrodiene compounds (3, 4a, 5a,b, 6c, 7a, 7c, 9) were obtained from the reactions of some thiols with 2-nitropentachloro-1,3-butadiene. N,S-Substituted nitrodiene compounds (11a-g, 13, 15) were obtained from 2-nitropentachloro-1,3-butadiene and some amines (morpholine and piperazine derivatives). The compound 4a was crystallized in the triclinic crystal system (space group P-1) with the unit cell parameters a = 6.6525(7) A, b = 10.7906(5) A, c = 10.8339(4) A, α = 72.57(3)°, β= 84.23(4)°, γ= 75.81(3)°, V= 719.03(9) A~3, Z = 2. The novel compounds were characterized by elemental analysis, UV-VIS, FT-IR,~1H-NMR, NMR (~(13)C or APT) and mass spectroscopy.
机译:在这项工作中,硫代取代的硝基二烯化合物(3、4a,5a,b,6c,7a,7c,9)是从一些硫醇与2-硝基五氯-1,3-丁二烯的反应中获得的。由2-硝基五氯-1,3-丁二烯和一些胺(吗啉和哌嗪衍生物)获得N,S取代的硝基二烯化合物(11a-g,13、15)。化合物4a在三斜晶系(空间群P-1)中晶格参数为a = 6.6525(7)A,b = 10.7906(5)A,c = 10.8339(4)A,α= 72.57( 3)°,β= 84.23(4)°,γ= 75.81(3)°,V = 719.03(9)A〜3,Z =2。通过元素分析,UV-VIS,FT-IR对这些新型化合物进行表征1 H-NMR,NMR(〜(13)C或APT)和质谱。

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