Matsumoto Kazuhiro, Oba Yuki, Nakajima Yumiko, Shimada Shigeru, Sato Kazuhiko
Interdisciplinary Research Center for Catalytic Chemistry (IRC3), National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba Central 5, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8565, Japan.
Angew Chem Int Ed Engl. 2018 Apr 16;57(17):4637-4641. doi: 10.1002/anie.201801031. Epub 2018 Mar 15.
Silicones (organopolysiloxanes) have found applications in a wide range of research areas, and their unique and valuable properties have rendered these materials virtually irreplaceable. Despite the fact that silicones have been employed industrially for more than 70 years, synthetic routes to generate silicones remain limited, and the sequence-controlled synthesis of oligo- and polysiloxanes still represents a major challenge in silicone chemistry. Described here is a highly selective sequence-controlled synthesis of linear, branched, and cyclic oligosiloxanes by simple iteration of two reactions, specifically, a B(C F ) -catalyzed dehydrocarbonative cross-coupling of alkoxysilanes with hydrosilanes and a B(C F ) -catalyzed hydrosilylation of carbonyl compounds, in a single flask. The sequence of the resulting oligosiloxanes can be controlled precisely by the order of addition of the hydrosilane monomers.
有机硅(聚有机硅氧烷)已在广泛的研究领域中得到应用,其独特且有价值的特性使得这些材料几乎不可替代。尽管有机硅已在工业上应用了70多年,但生成有机硅的合成路线仍然有限,并且低聚和聚硅氧烷的序列控制合成仍然是有机硅化学中的一个重大挑战。本文描述了一种通过在单个烧瓶中简单重复两个反应,即B(CF) -催化的烷氧基硅烷与氢硅烷的脱烃交叉偶联反应以及B(CF) -催化的羰基化合物的硅氢化反应,来高度选择性地合成线性、支化和环状低聚硅氧烷的方法。所得低聚硅氧烷的序列可以通过氢硅烷单体的添加顺序精确控制。