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具有延长烷基链的固定界面:通过固态核磁共振光谱对链序的比较研究。

Stationary interphases with extended alkyl chains: a comparative study on chain order by solid-state NMR spectroscopy.

作者信息

Pursch M, Brindle R, Ellwanger A, Sander L C, Bell C M, Händel H, Albert K

机构信息

Institut für Organische Chemie der Universität Tübingen, Germany.

出版信息

Solid State Nucl Magn Reson. 1997 Dec;9(2-4):191-201. doi: 10.1016/s0926-2040(97)00058-1.

Abstract

Stationary interphases with long n-alkyl chains (n = 18, 22, 30, 34) have been examined by solid-state NMR spectroscopy. The determination of the silane functionality and the degree of cross-linking of silane ligands on the silica surface was performed by 29Si CP/MAS NMR spectroscopy. High-speed 1H MAS and 13C CP/MAS NMR spectroscopy were utilized to assess alkyl chain order and mobility of the different bonded phases. For this purpose, 1H NMR line widths and 13C chemical shifts have been evaluated. It is shown that stationary phase order and rigidity increase with alkyl chain length. In addition, the temperature-dependent trans/gauche conformational change occurs at higher temperatures for a polymeric C34 phase compared with a C30 sorbent. This behaviour is discussed in the context of previously reported chromatographic (HPLC) shape selectivity differences.

摘要

通过固态核磁共振光谱对具有长正烷基链(n = 18、22、30、34)的固定相进行了研究。通过29Si CP/MAS核磁共振光谱测定了二氧化硅表面硅烷配体的硅烷官能度和交联度。利用高速1H MAS和13C CP/MAS核磁共振光谱评估了不同键合相的烷基链有序度和流动性。为此,对1H NMR线宽和13C化学位移进行了评估。结果表明,固定相的有序度和刚性随烷基链长度的增加而增加。此外,与C30吸附剂相比,聚合物C34相的反式/gauche构象变化在更高温度下发生。在先前报道的色谱(HPLC)形状选择性差异的背景下讨论了这种行为。

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