A solid-state NMR method for solution of zeolite crystal structures

被引:135
作者
Brouwer, DH
Darton, RJ
Morris, RE
Levitt, MH [1 ]
机构
[1] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England
[2] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
关键词
D O I
10.1021/ja052306h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Since zeolites are notoriously difficult to prepare as large single crystals, structure determination usually relies on powder X-ray diffraction (XRD). However, structure solution (i.e., deriving an initial structural model) directly from powder XRD data is often very difficult due to the diffraction phase problem and the high degree of overlap between the individual reflections, particularly for materials with the structural complexity of most zeolites. Here, we report a method for structure determination of zeolite crystal structures that combines powder XRD and nuclear magnetic resonance (NMR) spectroscopy in which the crucial step of structure solution is achieved using solid-state (29)Si double-quantum dipolar recoupling NMR, which probes the distance-dependent dipolar interactions between naturally abundant (29)Si nuclei in the zeolite framework. For two purely siliceous zeolite blind test samples, we demonstrate that the NMR data can be combined with the unit cell parameters and space group to solve structural models that refine successfully against the powder XRD data.
引用
收藏
页码:10365 / 10370
页数:6
相关论文
共 36 条
[1]   EXPO:: a program for full powder pattern decomposition and crystal structure solution [J].
Altomare, A ;
Burla, MC ;
Camalli, M ;
Carrozzini, B ;
Cascarano, GL ;
Giacovazzo, C ;
Guagliardi, A ;
Moliterni, AGG ;
Polidori, G ;
Rizzi, R .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1999, 32 :339-340
[2]  
Baerlocher C., 1978, DLS 76 PROGRAM SIMUL
[3]   Structure of ITQ-4, a new pure silica polymorph containing large pores and a large void volume [J].
Barrett, PA ;
Camblor, MA ;
Corma, A ;
Jones, RH ;
Villaescusa, LA .
CHEMISTRY OF MATERIALS, 1997, 9 (08) :1713-&
[4]   Symmetry-based 29Si dipolar recoupling magic angle spinning NMR spectroscopy:: A new method for investigating three-dimensional structures of zeolite frameworks [J].
Brouwer, DH ;
Kristiansen, PE ;
Fyfe, CA ;
Levitt, MH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (02) :542-543
[5]   An X-ray diffraction and MAS NMR study of the thermal expansion properties of calcined siliceous ferrierite [J].
Bull, I ;
Lightfoot, P ;
Villaescusa, LA ;
Bull, LM ;
Gover, RKB ;
Evans, JSO ;
Morris, RE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (14) :4342-4349
[6]   Structure solution of zeolites from powder diffraction data [J].
Burton, AW .
ZEITSCHRIFT FUR KRISTALLOGRAPHIE, 2004, 219 (12) :866-880
[7]   Synthesis of all-silica and high-silica molecular sieves in fluoride media [J].
Camblor, MA ;
Villaescusa, LA ;
Díaz-Cabañas, MJ .
TOPICS IN CATALYSIS, 1999, 9 (1-2) :59-76
[8]   Structure of a protein determined by solid-state magic-angle-spinning NMR spectroscopy [J].
Castellani, F ;
van Rossum, B ;
Diehl, A ;
Schubert, M ;
Rehbein, K ;
Oschkinat, H .
NATURE, 2002, 420 (6911) :98-102
[9]   Supramolecular self-assembled molecules as organic directing agent for synthesis of zeolites [J].
Corma, A ;
Rey, F ;
Rius, J ;
Sabater, MJ ;
Valencia, S .
NATURE, 2004, 431 (7006) :287-290
[10]   A large-cavity zeolite with wide pore windows and potential as an oil refining catalyst [J].
Corma, A ;
Díaz-Cabañas, M ;
Martínez-Triguero, J ;
Rey, F ;
Rius, J .
NATURE, 2002, 418 (6897) :514-517