The iterative synthesis of discrete dimethylsiloxane oligomers: A practical guide

被引:17
|
作者
Lamers, Brigitte A. G.
de Waal, Bas F. M.
Meijer, E. W. [1 ]
机构
[1] Tech Univ Eindhoven, Inst Complex Mol Syst, POB 513, NL-5600 MB Eindhoven, Netherlands
关键词
dimethylsiloxane; discrete oligomers; iterative synthesis; Karstedt' s catalyst; silicon NMR; CO-OLIGOMERS; SILANOLS; STRATEGY; HYDROSILYLATION; FABRICATION; MECHANISM; CATALYSIS; OLEFINS; PDMS;
D O I
10.1002/pol.20200649
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Discrete dimethylsiloxane oligomers are interesting building blocks for the synthesis of high chi-low N block co-oligomers (BCOs) forming highly organized nanostructures. Here, a practical guide to the synthesis of molecularly defined oligodimethylsiloxanes (oDMS) from 7-mer to 40-mer via a linear growth strategy is described. The iteration of a hydroxylation reaction and the condensation of mono- or bifunctional hydroxysiloxanes with chloro-octamethyltetrasiloxane results in asymmetric and symmetric siloxanes, respectively. The synthesis contains critical washing and purification steps to remove minor amounts of low and high-molecular weight byproducts, which are detected using Fourier transform infrared spectrometry, gas chromatography-mass spectrometry, and size-exclusion chromatography. The oligomers are obtained on a multigram scale in yields of 94-50% and in high purity with only one molar mass detected. The formation of the chloride, hydroxide or hydride functional groups is adequately analyzed using Si-29 NMR spectroscopy. The hydride terminated siloxane oligomers are used in Karstedt catalyzed hydrosilylation reactions with alkene-functional substrates to obtain oDMS-based oligomers and BCOs. Byproduct formation as a result of isomerization and reduction are followed by H-1 NMR spectroscopy and minimized using dry conditions and low-catalyst loadings.
引用
收藏
页码:1142 / 1150
页数:9
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