Ionothermal 17O enrichment of oxides using microlitre quantities of labelled water

被引:50
作者
Griffin, John M. [1 ]
Clark, Lucy [1 ]
Seymour, Valerie R. [1 ]
Aldous, David W. [1 ]
Dawson, Daniel M. [1 ]
Iuga, Dinu [2 ]
Morris, Russell E. [1 ]
Ashbrook, Sharon E. [1 ]
机构
[1] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[2] Univ Warwick, Dept Phys, Coventry CV4 7AL, W Midlands, England
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
SOLID-STATE O-17; STRUCTURE DIRECTING AGENT; QUANTUM MAS NMR; 1ST-PRINCIPLES CALCULATIONS; QUADRUPOLAR NUCLEI; DOUBLE-ROTATION; IONIC LIQUIDS; RESOLUTION; ZEOLITE; PARAMETERS;
D O I
10.1039/c2sc20155k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We present an ionothermal-based method for the simple and low-cost enrichment in O-17 of oxide materials. This is demonstrated for the case of SIZ-4, an ionothermally-prepared aluminophosphate framework with the CHA topology. A preliminary study of unenriched samples of SIZ-4 highlights the importance of the careful choice of template in order to obtain an ordered structure. We then show how an ionothermal synthesis procedure incorporating microlitre quantities of O-17-enriched H2O enables as-prepared and calcined samples of SIZ-4 to be obtained with O-17 enrichment levels that are sufficient to enable the recording of high-quality O-17 solid-state NMR spectra. While second-order quadrupolar-broadened resonances are unresolved in O-17 MAS NMR spectra, O-17 double-rotation (DOR) and multiple-quantum (MQ) MAS NMR spectra reveal distinct resonances that are partially assigned by comparison with NMR parameters derived using first-principles calculations. The calculations also enable an investigation of the dependence of O-17 NMR parameters on the local structural environment. We find that both the O-17 isotropic chemical shift and quadrupolar coupling constant show clear dependencies on Al-O-P bond lengths, and angles and will therefore provide a sensitive probe of structure and geometry in aluminophosphate frameworks in future studies.
引用
收藏
页码:2293 / 2300
页数:8
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