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Synthesis,Crystal Structure and Insecticidal Activity of N-(pyridin-2-ylmethyl)-1-phenyl-1,4,5,6,7,8-hexahydrocyclohepta[c]pyrazole-3-carboxamide

Synthesis,Crystal Structure and Insecticidal Activity of N-(pyridin-2-ylmethyl)-1-phenyl-1,4,5,6,7,8-hexahydrocyclohepta[c]pyrazole-3-carboxamide

作     者:邓希乐 周小毛 王赞永 芮昌辉 杨新玲 

作者机构:Hunan Agriculture Biotechnology Research InstituteHunan Academy of Agricultural Sciences Department of Applied Chemistry College of ScienceChina Agricultural University Laboratory of Integrated Pest Management in Crops Ministry of AgricultureInstitute of Plant ProtectionChinese Academy of Agricultural Sciences 

出 版 物:《Chinese Journal of Structural Chemistry》 (结构化学(英文))

年 卷 期:2018年第37卷第4期

页      面:551-556页

核心收录:

学科分类:090403[农学-农药学(可授农学、理学学位)] 09[农学] 0904[农学-植物保护] 0703[理学-化学] 

基  金:financially supported by the National Key Research and Development Plan(No.2017YFD0200504) Hunan Provincial Science and Technology Plan Project(No.2016RS2012) 

主  题:synthesis bicyclic pyrazole amide crystal structure insecticidal activity 

摘      要:The title compound N-(pyridin-2-ylmethyl)- 1-phenyl- 1,4,5,6,7,8-hexahydrocy-clohepta[c]pyrazole-3-carboxamide 5 (C21I-I22N40, Mr = 346.42) has been synthesized andstructurally characterized by IR, 1H NMR, 13C NMR, H RMS and single-crystal X-raydiffraction. The crystal crystallizes in monoclinic system, space group P21/n with a = 8.668(2),b = 22.236(4), c = 9.539(2) A, β = 108.68(3)°, V = 1786.4(7)/k3, Z = 4, Dx= 1.288 g/cm3,F(000) = 736,μ(MoKa) = 0.649 mm^-1, the final R = 0.0354 and wR = 0.0933 with 3234observed reflections with I 〉 2σ(/). The benzene and pyrazole rings are nearly coplanar with adihedral angle of 50.977(46)°. The dihedral angle between the central pyrazole and pyridinerings is 11.688(46)°. No classical hydrogen bonds were found in the molecules. Two adjacentmolecules in crystal packing of compound 5 were linked by two intramolecularhydrogen-bonding interactions C(15)-H(15)…O(1) to generate a stable structure. Compound 5had weak insecticidal activity against the diamondback moth (Plutella xylostella), butexhibited good activity against cotton bollworm (Helicoverpa armigera).

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