2019
DOI: 10.1039/c9py00036d
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One-pot strategy for synthesis of open-cage silsesquioxane monomers

Abstract: A novel synthetic strategy to access POSS monomers has been proposed; one reaction site of an open-cage POSS was capped, and the remaining two silanol groups were functionalized for polymerization. Importantly, the monomer can be obtained by one-pot synthesis without any troublesome isolation process.

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Cited by 31 publications
(22 citation statements)
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“…−68 ppm for T type Si atoms (see Supplementary Materials, Figure S1b). It is in accordance with the data of compounds described by Naka et al [11]. Additionally, the important aspect of the synthetic procedure to ensure effective product formation was the proper cooling of the reaction mixture in an ice bath and the sequence of chlorosilane and amine addition.…”
Section: Resultssupporting
confidence: 89%
See 1 more Smart Citation
“…−68 ppm for T type Si atoms (see Supplementary Materials, Figure S1b). It is in accordance with the data of compounds described by Naka et al [11]. Additionally, the important aspect of the synthetic procedure to ensure effective product formation was the proper cooling of the reaction mixture in an ice bath and the sequence of chlorosilane and amine addition.…”
Section: Resultssupporting
confidence: 89%
“…On the other hand, open-cage silsesquioxanes, i.e., not-completely condensed systems have recently attracted much attention. The silsesquioxane trisilanol precursors enable the introduction of three reactive substituents to the Si-O-Si core by means of stoichiometric (hydrolytic condensation), but also catalytic (e.g., hydrosilylation, arylation, O-silylation), processes using functional groups that are already attached to the SQ core [8][9][10][11][12][13][14][15][16]. The symmetry of their trifunctional T 7 open-cage derivatives is changed due to the lack of one vertex in the structure, which affects their physical properties (i.e., changes in molecular packing, melting points) [9,[17][18][19][20].…”
Section: Introductionmentioning
confidence: 99%
“…The EP-POSS resin was home-made in the laboratory; it was prepared by a condensation reaction with isopropanol (IPA), 5% tetramethylammonium hydroxide (TMAH) aqueous solution and γ-(2,3-glycidoxy) propyltrimethoxysilane (KH560), the specific preparation method is referred to in previous research [ 23 ]. The molecular structure of POSS is shown in Figure 1 .…”
Section: Methodsmentioning
confidence: 99%
“…[21][22][23] T7 can undergo corner-capping reaction with equal amount of R 0 SiX 3 which offers target functional groups, and finally generate mono-functional POSS. [24][25][26] This synthesis method ( Figure 3) has been widely used in the preparation of mono-functional POSS molecules. But the synthetic product of this method is mostly a mixture of various derivatives containing silicon hydroxyl groups, as well as diverse by-products, so it is difficult to separate and purify T7.…”
Section: Corner-capping Reactionmentioning
confidence: 99%