Schulz J, Roucoux A, Patin H
Laboratoire de Chimie Organique et des Substances Naturelles--CNRS ESA 6052, Ecole Nationale Superieure de Chimie de Rennes, France.
Chemistry. 2000 Feb 18;6(4):618-24. doi: 10.1002/(sici)1521-3765(20000218)6:4<618::aid-chem618>3.0.co;2-a.
A colloidal system based on an aqueous suspension of rhodium(o) nanoparticles proved to be an efficient catalyst for the hydrogenation of arene derivatives under biphasic conditions. The rhodium nanoparticles (2-2.5 nm) were synthesized by the reduction of RhCl3 x 3H2O with sodium borohydride and were stabilized by highly water-soluble N-alkyl-N-(2-hydroxyethyl)ammonium salts (HEA-Cn). These surfactant molecules were characterized by measurements of the surface tension and the aqueous dispersions with rhodium were observed by transmission electron cryomicroscopy. The catalytic system is efficient under ultramild conditions, namely room temperature and 1 atm H2 pressure. The aqueous phase which contains the protected rhodium(0) colloids can be reused without significant loss of activity. The microheterogeneous behavior of this catalytic system was confirmed on a mercury poisoning experiment.
基于铑(0)纳米颗粒水悬浮液的胶体体系被证明是在双相条件下芳烃衍生物氢化反应的高效催化剂。铑纳米颗粒(2 - 2.5纳米)通过硼氢化钠还原三水合氯化铑合成,并由高度水溶性的N - 烷基 - N -(2 - 羟乙基)铵盐(HEA - Cn)稳定。通过表面张力测量对这些表面活性剂分子进行了表征,并通过透射电子低温显微镜观察了铑在水中的分散情况。该催化体系在超温和条件下,即室温及1个大气压氢气压力下是有效的。含有被保护的铑(0)胶体的水相可以重复使用而活性无显著损失。该催化体系的微非均相行为在汞中毒实验中得到了证实。