HYDROGENATION OF PHENOL AND CRESOLS CATALYZED BY CHITOSAN SUPPORTED PALLADIUM COMPLEX AT MILD CONDITIONS
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HYDROGENATION OF PHENOL AND CRESOLS CATALYZED BY CHITOSAN SUPPORTED PALLADIUM COMPLEX AT MILD CONDITIONS
Vol. 14, Issue 1, Pages: 57-62(1996)
Affiliations:
1. Institute of Chemistry
2. Academia Sinica
3. Beijing 100080
Author bio:
Funds:
DOI:
CLC:O643.3
Published:20 March 1996
Accepted:
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[1]唐黎明,黄美玉,江英彦.HYDROGENATION OF PHENOL AND CRESOLS CATALYZED BY CHITOSAN SUPPORTED PALLADIUM COMPLEX AT MILD CONDITIONS[J].Chinese Journal of Polymer Science,1996(01):57-62.
TANG Liming, HUANG Meiyu, JIANG Yingyan. HYDROGENATION OF PHENOL AND CRESOLS CATALYZED BY CHITOSAN SUPPORTED PALLADIUM COMPLEX AT MILD CONDITIONS[J]. 1996, 14(1): 57-62.
[1]唐黎明,黄美玉,江英彦.HYDROGENATION OF PHENOL AND CRESOLS CATALYZED BY CHITOSAN SUPPORTED PALLADIUM COMPLEX AT MILD CONDITIONS[J].Chinese Journal of Polymer Science,1996(01):57-62.DOI:
TANG Liming, HUANG Meiyu, JIANG Yingyan. HYDROGENATION OF PHENOL AND CRESOLS CATALYZED BY CHITOSAN SUPPORTED PALLADIUM COMPLEX AT MILD CONDITIONS[J]. 1996, 14(1): 57-62.DOI:
HYDROGENATION OF PHENOL AND CRESOLS CATALYZED BY CHITOSAN SUPPORTED PALLADIUM COMPLEX AT MILD CONDITIONS
-CS-Pd) was found to catalyze the hydrogenation of phenol and cresols to correspond-ing cyclohexanones in high yield and 100% selectivity at 70℃ and 1.01325×10
5
Pa mildconditions. N/Pd molar ratio in the complex
temperature and solvents have much infiuenceon the reaction. The reactivity order of reactants was found to be: phenol
>
m-
>
p-
>
o-cresol. The catalyst is stable during the reaction and could be repeatedly used for severaltimes without much decrease in its catalytic activity.
-CS-Pd) was found to catalyze the hydrogenation of phenol and cresols to correspond-ing cyclohexanones in high yield and 100% selectivity at 70℃ and 1.01325×10
5
Pa mildconditions. N/Pd molar ratio in the complex
temperature and solvents have much infiuenceon the reaction. The reactivity order of reactants was found to be: phenol
>
m-
>
p-
>
o-cresol. The catalyst is stable during the reaction and could be repeatedly used for severaltimes without much decrease in its catalytic activity.
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