Solid-state 1H and 27Al NMR studies of DMSO-kaolinite intercalates

高岭石 插层(化学) 固态核磁共振 化学 魔角纺纱 核磁共振谱数据库 核磁共振波谱 离子键合 结晶学 八面体 质子核磁共振 分子 核磁共振 无机化学 晶体结构 立体化学 有机化学 离子 谱线 矿物学 物理 天文
作者
Jonathan Fafard,Victor V. Terskikh,Christian Detellier
出处
期刊:Clays and Clay Minerals [Cambridge University Press]
卷期号:65 (3): 206-219 被引量:14
标识
DOI:10.1346/ccmn.2017.064060
摘要

Abstract Nuclear magnetic resonance (NMR) provides a powerful tool to describe local nuclear environments. In this work, unique structural information on kaolinite and on kaolinite dimethylsulfoxide (DMSO) intercalate were provided by solid-state 1 H and 27 Al magic-angle spinning (MAS) NMR. The interlayer chemistry of kaolinite (K) was examined by intercalating a select group of highly polar organic molecules or salts into kaolinite as a first step. Once the interlayer space is expanded, the intercalated compounds can be replaced in a second step. Intercalating DMSO into kaolinite to form the DMSO-K intercalate is, thus, a particularly useful first step toward the intercalation of a large variety of molecules, including polymers and ionic liquids. Well developed characterization methods are essential to define the structural modifications of kaolinite, and MAS NMR is a useful complement to other techniques. The use of 1 H and 27 Al MAS NMR for this purpose has been relatively rare. 1 H NMR, nevertheless, can give unique information about kaolinite hydroxyls. Because quadrupolar interactions are sensitive to the local octahedral Al(III) geometry, solid-state 27 Al NMR can follow subtle structural modifications in the octahedral sheet. In the present work, the 1 H MAS NMR chemical shifts of KGa-1b were unambiguously attributed to the internal surface hydroxyls at 2.7 ppm and to the internal hydroxyls at 1.7 ppm. The 1 H MAS NMR chemical shifts of the two methyl groups in DMSO-K are not equivalent and can be attributed to the 2.9 and 4.2 ppm peaks. The 27 Al MAS NMR spectra of KGa-1b obtained under different magnetic fields revealed that most of the quadrupolar effects were highly reduced at 21.1 T, whereas the spectra at lower field, 4.7 T, were dominated by quadrupolar effects. The two octahedral Al(III) sites are not equivalent and can be distinguished in the low-field spectral simulation. Increased quadrupolar constants were observed and showed the major perturbations of the local Al symmetry that resulted from DMSO intercalation. Both the 1 H and 27 Al MAS NMR studies at different magnetic fields afforded important information about the local environments of the kaolinite hydroxyl groups and structural Al(III).
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