PREPARATION AND CATALYTIC BEHAVIOUR OF POLYMER-BOUND METALLOPORPHYRIN IN HYDROGENATION OF OLEFIN
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PREPARATION AND CATALYTIC BEHAVIOUR OF POLYMER-BOUND METALLOPORPHYRIN IN HYDROGENATION OF OLEFIN
Vol. 16, Issue 1, Pages: 91-96(1998)
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Published:20 March 1998
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WANG Rongmin, HE Yufeng, LEI Ziqiang, et al. PREPARATION AND CATALYTIC BEHAVIOUR OF POLYMER-BOUND METALLOPORPHYRIN IN HYDROGENATION OF OLEFIN[J]. 1998, 16(1): 91-96.
DOI:
WANG Rongmin, HE Yufeng, LEI Ziqiang, et al. PREPARATION AND CATALYTIC BEHAVIOUR OF POLYMER-BOUND METALLOPORPHYRIN IN HYDROGENATION OF OLEFIN[J]. 1998, 16(1): 91-96.DOI:
PREPARATION AND CATALYTIC BEHAVIOUR OF POLYMER-BOUND METALLOPORPHYRIN IN HYDROGENATION OF OLEFIN
The meso- tetraarylporphyrin has been anchored to styrene- divinylbenzenecopolymers by reaction of meso- tetra (4-hydroxylphenyl ) porphyrin with chloromethylatedresin under mild condition. A number of polymer transition metal complexes have beenprepared with the polymer ligand and metal salts. The polymeric ligand and its complexeshave been characterized by electronic spectra
and vibrational spectra. Cyclohexene can behydrogenated 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 intro groups
carbonyl groups and olefins with steric hindrance substityents
and showed no activity for aromatic rings under these conditions.
Abstract
The meso- tetraarylporphyrin has been anchored to styrene- divinylbenzenecopolymers by reaction of meso- tetra (4-hydroxylphenyl ) porphyrin with chloromethylatedresin under mild condition. A number of polymer transition metal complexes have beenprepared with the polymer ligand and metal salts. The polymeric ligand and its complexeshave been characterized by electronic spectra
and vibrational spectra. Cyclohexene can behydrogenated 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 intro groups
carbonyl groups and olefins with steric hindrance substityents
and showed no activity for aromatic rings under these conditions.
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