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Preparation and catalytic behaviour of polymer-bound metalloporphyrin in hydrogenation of olefin

机译:聚合物键合金属卟啉在烯烃加氢中的制备及催化性能

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摘要

The meso-tetraarylporphyrin has been anchored to styrene styrene-divinylbenzene copolymers by reaction of 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.
机译:通过使内消旋四(4-羟苯基)卟啉与氯甲基化树脂在温和的条件下反应,将内消旋四芳基卟啉锚定在苯乙烯-苯乙烯-二乙烯基苯共聚物上。已经用聚合物配体和金属盐制备了许多聚合物过渡金属配合物。聚合物配体及其配合物已通过电子光谱和振动光谱表征。环己烯可以用聚合卟啉钯配合物(P-THPPPd)进行氢化,其催化活性受溶剂的极性,乙醇中水的含量或反应温度的影响。然而,其对硝基,羰基和具有位阻取代基的烯烃的催化活性较低,在这些条件下对芳环没有活性。

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