Conley Matthew P, Rossini Aaron J, Comas-Vives Aleix, Valla Maxence, Casano Gilles, Ouari Olivier, Tordo Paul, Lesage Anne, Emsley Lyndon, Copéret Christophe
Department of Chemistry and Applied Biosciences, Vladimir Prelog Weg 2 ETH Zürich, CH-8093 Zürich, Switzerland.
Phys Chem Chem Phys. 2014 Sep 7;16(33):17822-7. doi: 10.1039/c4cp01973c.
Grafting reactive molecular complexes on dehydroxylated amorphous silica is a strategy to develop "single-site" heterogeneous catalysts. In general, only the reactivity of isolated silanols is invoked for silica dehydroxylated at 700 °C ([SiO(2-700)]), though ca. 10% of the surface silanols are in fact geminal Q2-silanols. Here we report the reaction of allyltributylstannane with [SiO(2-700)] and find that the geminal Q2-silanols react to form products that would formally arise from vicinal Q3-silanols that are not present on [SiO(2-700)], indicating that a surface rearrangement occurs. The reorganization of the silica surface is unique to silica dehydroxylated at 700 °C or above. The findings were identified using Dynamic Nuclear Polarization Surface Enhanced NMR Spectroscopy (DNP SENS) combined with DFT calculations.
将反应性分子络合物接枝到脱羟基无定形二氧化硅上是开发“单中心”多相催化剂的一种策略。一般来说,对于在700℃脱羟基的二氧化硅([SiO(2 - 700)]),通常仅考虑孤立硅醇的反应性,尽管实际上约10%的表面硅醇是孪位Q2 - 硅醇。在此我们报道烯丙基三丁基锡与[SiO(2 - 700)]的反应,并发现孪位Q2 - 硅醇反应形成的产物,形式上应由[SiO(2 - 700)]上不存在的邻位Q3 - 硅醇产生,这表明发生了表面重排。二氧化硅表面的这种重组是700℃及以上脱羟基二氧化硅所特有的。这些发现是通过动态核极化表面增强核磁共振光谱(DNP SENS)结合密度泛函理论计算确定的。