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机构地区:[1]Department of Chemistry, Northwest Normal University, Lanzhou 730070 China OSSO Key State Laboratory, Lanzhou Institute of Chemical Physics, The Chinese Academy of Sciences, Lanzhou, 730000, China [2]Department of Chemistry, Northwest Normal University, Lanzhou 730070 China [3]OSSO Key State Laboratory, Lanzhou Institute of Chemical Physics, The Chinese Academy of Sciences, Lanzhou, 730000, China
出 处:《Chinese Journal of Polymer Science》1998年第1期91-96,共6页高分子科学(英文版)
基 金:This work was supported by the National Natural Science Foundation of China.
摘 要:The meso-tetraarylporphyrin has been anchored to styrene-divinylbenzene copolymers by reaction or meso-tetra(4-hydroxylphenyl) porphyrin with chloromethylated resin under mild condition. A number of polymer transition metal complexes have been prepared with the polymer ligand and metal salts. The polymeric ligand and its complexes have been characterized by electronic spectra, and vibrational spectra. Cyclohexene can be hydrogenated with the polymeric porphyrin palladium complex(P-THPPPd) as catalyst, and its catalytic activity was influenced by the polarity of solvents, the contents of water in ethanol or reaction temperature. However, its catalytic activity was lower for nitro groups, carbonyl groups and olefins with steric hindrance substituents, and showed no activity for aromatic rings under these conditions.The meso-tetraarylporphyrin has been anchored to styrene-divinylbenzene copolymers by reaction or meso-tetra(4-hydroxylphenyl) porphyrin with chloromethylated resin under mild condition. A number of polymer transition metal complexes have been prepared with the polymer ligand and metal salts. The polymeric ligand and its complexes have been characterized by electronic spectra, and vibrational spectra. Cyclohexene can be hydrogenated with the polymeric porphyrin palladium complex(P-THPPPd) as catalyst, and its catalytic activity was influenced by the polarity of solvents, the contents of water in ethanol or reaction temperature. However, its catalytic activity was lower for nitro groups, carbonyl groups and olefins with steric hindrance substituents, and showed no activity for aromatic rings under these conditions.
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