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Y. X. Sun, Y. Guo, Q. Z. Lu, X. L. Meng, X. H. Wu, Y. L. Guo, Y. S. Wang, X. H. Liu and Z. G. Zhang, “Highly Selective Asymmetry Transfer Hydrogenation of Pro- chiral Acetophenone Catalyzed by Palladium-Chitosan on Silica,” Catalsis Letter, Vol. 100, No. 3-4, 2005, pp. 213-217. doi:10.1007/s10562-004-3458-1

has been cited by the following article:

• TITLE: Efficient and Clean Catalytic Hydrogenolysis of Aromatic Ketones by Silica Supported Schiff Base Modify Chitosan-Palladium Catalyst

  AUTHORS: Tingting Gu, Lijun Liu, Changqiu Zhao

  KEYWORDS: CS-Schiff-Base; Pd Catalyst; Hydrogen; Aromatic Ketones

  JOURNAL NAME: Modern Research in Catalysis, Vol.2 No.1, January 28, 2013

  ABSTRACT: An silica supported chitosan-Schiff base Pd(II) catalyst was prepared in a simple way and characterized by XRD, FT-IR, SEM-EDS, XPS and TG, and the ability of this complex to catalyze hydrogenolysis of 1-tetralone into 1,2,3,4-tetrahydronaphthalene was also investigated in the presence of hydrogen. It has been revealed that the catalyst had high catalytic activity for hydrogenolysis of 1-tetralone at ambient temperature and normal pressure of hydrogen. Especially, the hydrogenolysis of 1-tetralone in ethanol solvent gave excellent results and the 100% conversion of 1-tetralone and the 100% selectivity for 1,2,3,4-tetrahydronaphthalene were obtained under optimized reaction conditions. The influences of reaction temperature, reaction time and solvent on the hydrogenolysis of 1-tetralone were also investigated. It has been also revealed that the catalyst was efficient and eco-friendly for the hydrogenolysis of carbonyl that connected with a benzene ring to give corresponding aromatic hydrocarbons.