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二苄基锡N,N-二甲基氨荒酸酯的合成及晶体结构
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作者 尹汉东 王传华 马春林 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2004年第3期316-319,共4页
利用二苄基二氯化锡和N, N-二甲基氨荒酸钠反应, 合成了二苄基锡N, N-二甲基氨荒酸酯(C20H26N2S4Sn, Mr = 541.36)。通过元素分析、红外光谱、核磁共振氢谱和质谱对其结构进行了表征。用X-射线单晶衍射测定了该化合物的晶体结构。化合... 利用二苄基二氯化锡和N, N-二甲基氨荒酸钠反应, 合成了二苄基锡N, N-二甲基氨荒酸酯(C20H26N2S4Sn, Mr = 541.36)。通过元素分析、红外光谱、核磁共振氢谱和质谱对其结构进行了表征。用X-射线单晶衍射测定了该化合物的晶体结构。化合物为单斜晶系, 空间群P21/n, a = 1.3926(5), b = 0.9832(4), c = 1.7080(7) nm, b = 103.541(6), V = 2.274(2) nm3, Z = 4, Dc = 1.581 g/cm3, m(MoKa) = 1.500 mm-1, F(000) = 1096, R = 0.0482, wR = 0.1162. 在化合物的晶体中, 锡原子为六配位的畸变八面体构型。 展开更多
关键词 二苄基锡n n-二甲基氨荒酸酯 合成 晶体结构 二苄基二氯化锡 n n-二甲基氨荒酸钠
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二苄基N,N二甲基荒酸锡的合成及晶体结构研究(英文)
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作者 朱德中 张如芬 +1 位作者 尹汉东 马春林 《合成化学》 CAS CSCD 2002年第2期126-130,共5页
用二苄基二氯化锡与N ,N 二甲基荒酸钠反应合成了化合物 (PhCH2 ) 2 Sn[S2 CN(CH3) 2 ]2 ,通过X 射线确定了其晶体结构 ,晶胞参数为 :单斜晶系 ,空间群P2 1/n ,a =13.92 6 (5 ) ,b =9.832 (4) ,c =17.0 80 (7) ,β =10 3.5 41(6 )... 用二苄基二氯化锡与N ,N 二甲基荒酸钠反应合成了化合物 (PhCH2 ) 2 Sn[S2 CN(CH3) 2 ]2 ,通过X 射线确定了其晶体结构 ,晶胞参数为 :单斜晶系 ,空间群P2 1/n ,a =13.92 6 (5 ) ,b =9.832 (4) ,c =17.0 80 (7) ,β =10 3.5 41(6 )° ,V =2 2 73.7(15 ) 3,Z 展开更多
关键词 晶体结构 合成 二苄基n n-二甲基荒酸锡 有机锡化合物
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Synthesis,Crystal Structure and Characterization of a New Mixed-valence Cu(Ⅰ)/Cu(Ⅱ) Complex [Cu(bipy)(Me_2dtc)CuI_2]_n
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作者 范乐庆 吴季怀 +1 位作者 黄昀昉 林建明 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2011年第3期340-345,共6页
A new one-dimensional mixed-valence Cu(Ⅰ)/Cu(Ⅱ) complex [Cu(bipy)(Me2dtc)CuI2]n 1 (bipy = 2,2′-bipyridine and Me2dtc = N,N-dimethyldithiocarbamate) has been synthesized under solution condition, and chara... A new one-dimensional mixed-valence Cu(Ⅰ)/Cu(Ⅱ) complex [Cu(bipy)(Me2dtc)CuI2]n 1 (bipy = 2,2′-bipyridine and Me2dtc = N,N-dimethyldithiocarbamate) has been synthesized under solution condition, and characterized by elemental analysis, IR spectrum, single-crystal X-ray diffraction and magnetic property. The crystal belongs to the tetragonal system, space group P4122 with a = b = 11.6504(16), c = 13.466(3) A, V = 1827.8(5) A^3, Z = 4, Dc = 2.389 g/cm^3, Mr = 657.27, λ(MoKa) = 0.71073 , μ = 5.931 mm·1, F(000) = 1236, the final R = 0.0483 and wR = 0.1245. A total of 2102 unique reflections were collected, of which 2009 with I 〉 2σ(I) were observed. 1 consists of polymeric [Cu^II2]nn^- anions and [Cu^II(bipy)(Me2dtc)]^+ cations. It is interesting that the cations of 1 interact through π-π stacking interactions after rotating 90° to form one-dimensional chains parallel to the anion chains. The magnetic study indicates antiferromagnetic behavior for this complex. 展开更多
关键词 Cu(I)/Cu(II) n n-dimethyldithiocarbamate 2 2'-bipyridine crystal structure π-π packing interactions magnetic study
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Synthesis,Structure and Biological Activities of S-[α-(4-Methoxyphenylcarbonyl)-2-(1,2,4-triazole-1-yl)] ethyl-N,N-dime-thyldithiocarbamate
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作者 许良忠 建方方 +1 位作者 高红荣 朱崇毅 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2003年第12期1615-1618,共4页
The title compound was prepared by reaction of N,N -dimethyldithiocarbamate sodium with 1-bromo-1-(4-meth^oxy^phenylcarbonyl)-2-( 1,2,4 -triazole-1-yl)ethane. Its crystal structure has been determined by X-ray diff... The title compound was prepared by reaction of N,N -dimethyldithiocarbamate sodium with 1-bromo-1-(4-meth^oxy^phenylcarbonyl)-2-( 1,2,4 -triazole-1-yl)ethane. Its crystal structure has been determined by X-ray diffraction analysis. The crystal belongs to triclinic with space group P1-,a=0.7339(2) nm,b=1.1032(2) nm,c=1.1203(2) nm,α=90.27(3)°,β=102.03(3)°,γ=104.91(3)°,Z=2,V=0.8556(3) nm 3,D_c=1.360 g/cm 3,μ=0.325 mm -1 ,F(000)=368,final R_1=0.0475. The planes of 4-methoxybenzyl group and triazole ring are nearly perpendicular to each other. The dihedral angle is 83.97°. There is an obvious π-π stacking interaction between the molecules in the crystal lattice. The results of biological test show that the title compound has fungicidal and plant growth regulating activities. 展开更多
关键词 n n-dimethyldithiocarbamate 1 2 4 -triazole crystal structure biological activity
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