化学
反应性(心理学)
丙酮
核磁共振波谱
硅氧烷
亚胺
质子核磁共振
光谱学
氟-19核磁共振
二维核磁共振波谱
水解
碳-13核磁共振卫星
高分子化学
有机化学
催化作用
立体化学
物理
病理
替代医学
聚合物
医学
量子力学
作者
Pierluigi Mazzei,L. Fusco,Alessandro Piccolo
摘要
We followed the reactivity of acetone with 3‐aminopropyltrimethoxysilane, a potential organosilane coupling agent, by 1 H, 13 C and 29 Si NMR spectroscopy. Selective 1D and 2D‐edited NMR experiments significantly contributed to simplify the spectral complexity of reaction solution and elucidated molecular structures within progressive reaction phases. The course of the 3‐aminopropyltrimethoxysilane reaction with acetone was shown by a progressive decrease of both reactants, and a concomitant appearance of water and methanol, due to formation of imine and hydrolysis of alkoxysilane groups, respectively. The occurrence of multiple siloxane linkages in a progressively larger cross‐linked macromolecular structure was revealed by DOSY‐NMR experiments and new signals in 29 Si‐NMR spectra at different reaction times. The NMR approach described here may be applied to investigate the reactivity of other γ‐aminopropylalkoxysilanes and contribute to define procedures for the preparation of silica‐based materials. Copyright © 2014 John Wiley & Sons, Ltd.
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