Optimized synthesis of functional organosilicon monomers and polymers exploiting new types of CuAAC recoverable heterogeneous catalysts

被引:6
作者
Bezlepkina, Kseniya A. [1 ,3 ]
Belikova, Irina I. [1 ,2 ]
Aristova, Vasilissa A. [1 ,2 ]
Klokova, Kseniia S. [1 ]
Ardabevskaia, Sofia N. [1 ,3 ]
Pereyaslavtsev, Alexander Yu [4 ]
Migulin, Dmitry A. [1 ]
Milenin, Sergey A. [1 ,3 ]
机构
[1] Russian Acad Sci, Enikolopov Inst Synthet Polymer Mat, Moscow 117393, Russia
[2] Mendeleev Univ Chem Technol Russia, Moscow 125047, Russia
[3] Tula State Lev Tolstoy Pedag Univ, Res Lab New Silicone Mat & Technol, Tula 300026, Russia
[4] RAS, A N Nesmeyanov Inst Organoelement Cpds, Moscow 119991, Russia
基金
俄罗斯科学基金会;
关键词
CLICK-CHEMISTRY; SILICA; SILYLATION; DENDRIMERS; ROUTE; CU;
D O I
10.1039/d3re00532a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Organosilicon molecules of both individual and polymer structures are an integral part of modern high-tech industrial production and high technologies. The creation of simple methods for the synthesis of such molecules must meet modern environmental and economic standards. This work demonstrates for the first time the possibility of creating a number of functional organosilicon molecules from organoalkoxysilanes to polydimethylsiloxanes and carbosilane dendrimers using the reaction of Cu(i) catalyzed azide-alkyne cycloaddition (CuAAC) in its heterogeneous version. All processes were carried out until complete conversion of functional groups in the composition of organosilicon molecules without the use of solvents or amines and at a relatively low temperature - 60 degrees C. An important result of this work is the study of the leaching of copper from a heterogeneous catalyst into the final polysiloxanes and the assessment of their potential toxicity towards biological cells in comparison with polysiloxane modified by the CuAAC reaction catalyzed by a copper salt(i). Organosilicon molecules of both individual and polymer structures are an integral part of modern high-tech industrial production and high technologies.
引用
收藏
页码:448 / 460
页数:13
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