...
首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Bio-inspired Mo(II) complexes as active catalysts in homogeneous and heterogeneous olefin epoxidation
【24h】

Bio-inspired Mo(II) complexes as active catalysts in homogeneous and heterogeneous olefin epoxidation

机译:受生物启发的Mo(II)配合物在均相和非均相烯烃环氧化中作为活性催化剂

获取原文
获取原文并翻译 | 示例

摘要

New hydrotalcite clay materials functionalized with molybdenum(II) complexes holding potential catalytic properties were prepared by a stepwise procedure. The material was first calcined at 823 K for 4 h, to. eliminate all the carbonate ions; the layered structure was reconstructed after treatment with a solution of either tryptophane (trpH) or phenylalanine (pheH) in a KOH aqueous solution of dmf at 343 K. Subsequent impregnation with a solution of the organometallic precursor [Mol2(CO)3(NCCH3)2] led to substitution of the nitriles by the ligands affording the organometallic derivatized clays. The equivalent homogeneous phase complexes [MoI2(CO)3L] (L=trpH or pheH) were also prepared for comparison purposes. All the materials were characterized by powder X-ray diffraction, FTIR and ~(13)C CP MAS-DD solid state NMR. The complexes were also characterized by FTIR, UV/vis, elemental analysis, and ~1H and ~(13)C solution NMR accordingly. Both the complexes and these new materials, the latter containing 3.90 wt.% and 5.42 wt.% of Mo, respectively for HT-trp-Mo and HT-phe-Mo materials, catalyzed the epoxidation of cyclooctene and styrene at 328 K. The heterogeneous catalytic systems performed better showing that the presence of the clay is not innocent. In addition, further oxidation of styrene yielding benzaldehyde has occurred. A possible mechanism is proposed based on the detection of two reaction intermediaries by GC/MS. The heterogeneous catalysts also show superior handling capabilities due to Mo increased resistance to moisture and to separation from reaction medium.
机译:通过逐步程序制备了具有潜在催化性能的钼(II)配合物官能化的新型水滑石粘土材料。首先将该材料在823 K下煅烧4 h。消除所有碳酸根离子;在色氨酸(trpH)或苯丙氨酸(pheH)在dmf的KOH水溶液中于343 K处理后,重建了层状结构。随后用有机金属前体[Mol2(CO)3(NCCH3) 2]导致腈被配体取代,得到有机金属衍生的粘土。还准备了等效的均相复合物[MoI2(CO)3L](L = trpH或pheH)用于比较。所有材料均通过粉末X射线衍射,FTIR和〜(13)C CP MAS-DD固态NMR表征。还通过FTIR,UV / vis,元素分析和〜1H和〜(13)C溶液NMR表征了配合物。配合物和这些新材料(对于HT-trp-Mo和HT-phe-Mo材料,后者分别包含3.90 wt。%和5.42 wt。%的Mo)都催化了328 K下环辛烯和苯乙烯的环氧化。非均相催化体系表现更好,表明粘土的存在不是无害的。此外,苯乙烯进一步氧化生成苯甲醛。根据GC / MS对两种反应中间体的检测,提出了一种可能的机理。由于Mo增强了对水分的抗性以及与反应介质的分离性,因此多相催化剂还显示出卓越的处理能力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号