Institute for Molecular Science, Okazaki, Japan.
Dalton Trans. 2011 Mar 14;40(10):2338-47. doi: 10.1039/c0dt00950d. Epub 2010 Dec 17.
Molecularly imprinted Ru-complex catalysts acting in water were prepared on a SiO(2) surface by molecular imprinting of a SiO(2)-supported Ru-complex using organic polymers as surface matrix overlayers. (R)-1-(o-fluorophenyl)ethanol, which is one of the hydrogenated products of o-fluoroacetophenone, was imprinted on the supported Ru-complex as a template, and an active Ru-complex with a shape-selective reaction space (molecularly imprinted cavity) was prepared inside the wall of the hydrophobic organic polymer matrix overlayers. Structures of the SiO(2)-supported and molecularly imprinted Ru catalysts were characterized by means of solid-state NMR, XPS, XRF, ICP, UV/vis, XAFS, TGA, and SEM. The molecularly imprinted Ru catalysts exhibited fine shape selectivity and enantioselectivity for the asymmetric transfer hydrogenation of o-fluoroacetophenone and its derivatives.
通过使用有机聚合物作为表面基质覆盖层,在 SiO2 表面上通过 SiO2 负载的 Ru 配合物的分子印迹制备了在水中起作用的分子印迹 Ru 配合物催化剂。(R)-1-(邻氟苯基)乙醇是邻氟苯乙酮的氢化产物之一,被印迹在负载的 Ru 配合物上作为模板,并且在疏水性有机聚合物基质覆盖层的壁内制备了具有形状选择性反应空间(分子印迹腔)的活性 Ru 配合物。通过固态 NMR、XPS、XRF、ICP、UV/vis、XAFS、TGA 和 SEM 对 SiO2 负载和分子印迹 Ru 催化剂的结构进行了表征。分子印迹 Ru 催化剂对邻氟苯乙酮及其衍生物的不对称转移氢化表现出精细的形状选择性和对映选择性。