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机构地区:[1]StateKeyLaboratoryforOxoSynthesisandSelectiveOxidation,LanzhouInstituteofChemicalPhysics,TheChineseAcademyofSciences,Lanzhou730000,China [2]ShanghaiInstituteofOrganicChemistry,TheC
出 处:《Chinese Journal of Structural Chemistry》2002年第5期489-492,共4页结构化学(英文)
基 金:This work was supported by the National Natural Science Foundation of China(29871061)
摘 要:The new chiral cluster [NiRuMo(CO)5(m3-S)(h5-C5H5)(h5-C5H4COCH3)] 3 was synthesized by the reaction of precursor [CoRuMo(CO)8(m3-S)(h5-C5H4COCH3)] 1 with NiCp2 2 in refluxing THF. It was characterized by C/H elemental analysis, IR and 1H NMR. Molecular structure of cluster 3 was determined by single-crystal X-ray analyses. Crystal data: triclinic, space group P with the following crystallographic parameters: a = 7.9606(8), b = 8.5604(9), c = 14.779(2) , a = 93.908(2), b = 105.057(2), g = 101.463(2)? C17H12O6MoNiRuS, Mr = 600.05, Z = 2, V = 945.5(2) 3, Dc = 2.108 g/cm3, m = 2.568 mm-1, (2q )max ≤ 56.48, F(000) = 584,the final R = 0.0380 and wR = 0.0674 for 2995 observed reflections with I > 2.00s(I).The new chiral cluster [NiRuMo(CO)5(m3-S)(h5-C5H5)(h5-C5H4COCH3)] 3 was synthesized by the reaction of precursor [CoRuMo(CO)8(m3-S)(h5-C5H4COCH3)] 1 with NiCp2 2 in refluxing THF. It was characterized by C/H elemental analysis, IR and 1H NMR. Molecular structure of cluster 3 was determined by single-crystal X-ray analyses. Crystal data: triclinic, space group P with the following crystallographic parameters: a = 7.9606(8), b = 8.5604(9), c = 14.779(2) , a = 93.908(2), b = 105.057(2), g = 101.463(2)? C17H12O6MoNiRuS, Mr = 600.05, Z = 2, V = 945.5(2) 3, Dc = 2.108 g/cm3, m = 2.568 mm-1, (2q )max ≤ 56.48, F(000) = 584,the final R = 0.0380 and wR = 0.0674 for 2995 observed reflections with I > 2.00s(I).
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