首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >On the Use of CHClF2 as a Probe of Basic Sites in Zeolites:The Host-Guest Interactions Investigated by Multinuclear NMR
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On the Use of CHClF2 as a Probe of Basic Sites in Zeolites:The Host-Guest Interactions Investigated by Multinuclear NMR

机译:使用CHClF2作为沸石中基本位点的探针:多核NMR研究宿主与客体之间的相互作用

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摘要

The use of chlorodifluoromethane(CHClF2)as a probe molecule of zeolites basicity has been investigated by using infrared and multinuclear NMR spectroscopies and a series of alkali-exchanged faujasite with different Si/Al ratios(X and Y)and compensating cations of different nature.The ~1H NMR peak of adsorbed CHClF2 shifts to low fields and the CH stretching frequency(VCH)shifts to low wavenumbers as the zeolite basicity determined by the Sanderson method increases.Poorer linear correlation is observed for the v_(CH)band suggesting the occurrence of extra interactions of the fluorine atoms of the adsorbed chlorodifluoromethane with the nonframework cations.This interaction is evidenced for the first time by the spectroscopic modification of the probe molecule itself;~(19)F NMR chemical shifts and ~1J(C,F)spin-spin coupling constants are determined by the nature of the extraframework atoms and not by the framework basicity.The occurrence of the interactions between the fluoride atoms and the compensating cation does not allow quantifying the number of sites of similar basicity.
机译:通过红外和多核NMR光谱以及一系列具有不同Si / Al比(X和Y)和不同性质的补偿阳离子的碱交换八面沸石,研究了使用氯二氟甲烷(CHClF2)作为沸石碱度探针分子。随着桑德森法测定的沸石碱度增加,吸附的CHClF2的〜1H NMR峰移至低场,CH拉伸频率(VCH)移至低波数.v_(CH)谱带的线性相关性较差,表明发生了这种现象吸附的氯二氟甲烷中的氟原子与非骨架阳离子之间的额外相互作用,这种相互作用首次通过探针分子本身的光谱修饰得到证明;〜(19)F NMR化学位移和〜1J(C,F)自旋-自旋偶合常数是由骨架外原子的性质决定的,而不是由骨架的碱度决定的。补偿阳离子不允许量化相似碱性的位点数量。

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