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[Mn3O(O2CC6H5)6(C3H4N2)3]·C6H5CO2·0.5H2O的合成、晶体结构及磁性质
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作者 李君 张逢星 +1 位作者 唐宗薰 史启祯 《化学学报》 SCIE CAS CSCD 北大核心 2001年第7期1116-1120,共5页
Mn(O2CMe)2@4H2O、咪唑、苯甲酸和N(n-Bu)4MnO4在无水乙醇溶剂中反应,制备得到锰的三核μ3-O桥联配位化合物[Mn3O(O2CC6H5)6(C3H4N2)3]@C6H5CO2@0.5H2O.该配位化合物的X射线单晶衍射表明,其属于单斜晶系,空间群P21/C,晶胞参数:a=1.528 ... Mn(O2CMe)2@4H2O、咪唑、苯甲酸和N(n-Bu)4MnO4在无水乙醇溶剂中反应,制备得到锰的三核μ3-O桥联配位化合物[Mn3O(O2CC6H5)6(C3H4N2)3]@C6H5CO2@0.5H2O.该配位化合物的X射线单晶衍射表明,其属于单斜晶系,空间群P21/C,晶胞参数:a=1.528 32(19)nm,b=1.972 2(2)nm,c=2.102 3(3)nm,β=92.597(3)°,Z=4.变温磁化率(5~280 K)研究表明,该配位化合物中3个锰离子在低温下存在弱的反铁磁性耦合,交换积分J=-2.34cm-1. 展开更多
关键词 锰三核配位化合物 锰酶 [Mn3O(o2cc6h5)6(C3H4N2)3]·C6H5CO2·0.5H2O 绿色植物光系统Ⅱ 合成 晶体结构 磁化率 制备
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SYNTHESIS AND STRUCTURE OF TETRANUCLEAR MOLYBDENUM CLUSTER COMPOUND[Mo_4S_4(μ-O_2CC_6H_5)_2(dtp)_4]
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作者 Hong Hui ZHUANG Ding Ming WU Jian Quan HUANG Jin Ling HUANG Fuzhou Laboratory of Structure Chemistry and Fujian Institute of Research on the Structure of Matter,Chinese Academy of Sciences,Fuzhou 350002 《Chinese Chemical Letters》 SCIE CAS CSCD 1991年第7期553-554,共2页
The cluster compound[Mo_4S_4(μ-O_2CC_5H_5)_2(dtp)_4](dtp=S_2P(OEt)_2)was obtained by the ligand substitution reaction of tetranuclear molybdenum cluster [Mo_4S_4(μ-dtp)_2(dtp)_4]in the mixed solvent of acetone,ethan... The cluster compound[Mo_4S_4(μ-O_2CC_5H_5)_2(dtp)_4](dtp=S_2P(OEt)_2)was obtained by the ligand substitution reaction of tetranuclear molybdenum cluster [Mo_4S_4(μ-dtp)_2(dtp)_4]in the mixed solvent of acetone,ethanol and water in the presence of C_6H_5CO_2Na.It is monoclinic and crystallizes in space group C2/c, Mr=1495.09,a=12.175(5),b=22.01(1),c=20.875(9),β=99.04(4)°;V=5575(5);Z=4; Dc=1.78g/cm^3.Final R factor is 0.066.The result reveals that the[Mo_4S_4]cluster core and t-(dtp)^(-1)ligands are retained and only μ-bridged(dtp)^(-1)ligands are substituted by(C_6H_5CO_2)^(-1)in the substitution reaction,thus producing the new title cluster compound,the structure of which contains two species of bidentate ligand. 展开更多
关键词 MO DTP CO SYNTHESIS AND STRUCTURE OF TETRANUCLEAR MOLYBDENUM CLUSTER COMPOUND[Mo4S4 o2cc6h5 CC
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