• 文献标题:   Enhanced alkenes epoxidation reactivity of discrete bis(8-quinolinol)oxovanadium(IV) or bis(8-quinolinol)dioxomolybdenum(VI) tethered to graphene oxide by a metal-template/metal-exchange method
  • 文献类型:   Article
  • 作  者:   LI ZF, WU SJ, ZHENG DF, LIU H, HU J, SU HL, SUN J, WANG X, HUO QS, GUAN JQ, KAN QB
  • 作者关键词:   grapheme oxide, epoxidation, styrene, metaltemplate method, 8quinolinol complexe
  • 出版物名称:   APPLIED CATALYSIS AGENERAL
  • ISSN:   0926-860X EI 1873-3875
  • 通讯作者地址:   Jilin Univ
  • 被引频次:   17
  • DOI:   10.1016/j.apcata.2013.10.037
  • 出版年:   2014

▎ 摘  要

A series of imprinted catalysts were obtained by covalent attachment of discrete bis(8-quinolinol)oxovanadium(IV) or bis(8-quinolinol)dioxomolybdenum(VI) complex onto graphene oxide (GO) through the metal-template/metal-exchange method to control the distribution of covalently attached independent ligands, which were examined as catalysts in the epoxidation of alkenes using t-butylhydroperoxide (TBHP) or H2O2 as oxidant in comparison with their homogeneous counterparts and materials synthesized by random grafting of the ligand. The prepared catalysts were characterized by XRD, N-2 adsorption/desorption, TEM, FT-IR, diffusion reflection UV-visible, ICP-AES, TG, Raman, EPR, N element analysis and XPS. FT-IR, diffusion reflection UV-visible, ICP-AES, TG, N element analysis, Raman and XPS results showed that oxovanadium(IV) or dioxomolybdenum(VI) complexes were successfully grafted on GO. XRD, N-2 adsorption/desorption and TEM results indicated that the structures of the samples were well preserved. EPR results revealed that the materials synthesized by the metal-template method had better site-isolation compared with conventional materials. Furthermore, these imprinted oxovanadium(IV) or dioxomolybdenum(VI) complex catalysts are efficient and recyclable, which exhibit higher activity and higher selectivity to target product than either their homogeneous ones or randomly grafted analogues due to better site-isolation. (C) 2013 Elsevier B.V. All rights reserved.