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烷氧基硅烷化环硅氧烷的水解和分子内缩合合成多环和笼状硅氧烷。

Synthesis of Polycyclic and Cage Siloxanes by Hydrolysis and Intramolecular Condensation of Alkoxysilylated Cyclosiloxanes.

机构信息

Department of Applied Chemistry, Faculty of Science and Engineering, Waseda University, Okubo-3, Shinjuku-ku, Tokyo, 169-8555, Japan.

Kagami Memorial Research Institute, for Materials Science and Technology, Nishiwaseda-2, Shinjuku-ku, Tokyo, 169-0051, Japan.

出版信息

Chemistry. 2019 Feb 21;25(11):2764-2772. doi: 10.1002/chem.201805942. Epub 2019 Jan 25.

Abstract

The controlled synthesis of oligosiloxanes with well-defined structures is important for the bottom-up design of siloxane-based nanomaterials. This work reports the synthesis of various polycyclic and cage siloxanes by the hydrolysis and intramolecular condensation of monocyclic tetra- and hexasiloxanes functionalized with various alkoxysilyl groups. An investigation of monoalkoxysilylated cyclosiloxanes revealed that intramolecular condensation occurred preferentially between adjacent alkoxysilyl groups to form new tetrasiloxane rings. The study of dialkoxy- and trialkoxysilylated cyclotetrasiloxanes revealed multistep intramolecular condensation reactions to form cubic octasiloxanes in relatively high yields. Unlike conventional methods starting from organosilane monomers, intramolecular condensation enables the introduction of different organic substituents in controlled arrangements. So-called Janus cubes have been successfully obtained, that is, Ph R Si O , in which R=Me, OSiMe , and OSiMe Vi (Vi=vinyl). These findings will enable the creation of siloxane-based materials with diverse functions.

摘要

具有明确结构的低聚硅氧烷的可控合成对于基于硅氧烷的纳米材料的自下而上设计非常重要。本工作报道了通过各种烷氧基硅烷基官能化的单环四硅氧烷和六硅氧烷的水解和分子内缩合来合成各种多环和笼状硅氧烷。对单烷氧基硅烷基环硅氧烷的研究表明,分子内缩合优先在相邻的烷氧基硅烷基之间发生,形成新的四硅氧烷环。对二烷氧基和三烷氧基硅烷基环四硅氧烷的研究揭示了多步分子内缩合反应,以较高的产率形成立方八硅氧烷。与从有机硅烷单体开始的传统方法不同,分子内缩合能够以受控的方式引入不同的有机取代基。已经成功获得了所谓的 Janus 立方烷,即 PhRSiO ,其中 R=Me、OSiMe 和 OSiMeVi(Vi=乙烯基)。这些发现将能够创造具有多种功能的基于硅氧烷的材料。

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