A General Protocol for Determining the Structures of Molecularly Ordered but Noncrystalline Silicate Frameworks

被引:65
作者
Brouwer, Darren H. [1 ]
Cadars, Sylvian [2 ,3 ]
Eckert, Juergen [4 ]
Liu, Zheng [5 ]
Terasaki, Osamu [5 ]
Chmelka, Bradley F. [2 ]
机构
[1] Redeemer Univ Coll, Dept Chem, Ancaster, ON L9K 1J4, Canada
[2] Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 93106 USA
[3] Univ Orleans, CNRS, CEMHTI, UPR3079, F-45071 Orleans 2, France
[4] Univ S Florida, Dept Chem, Tampa, FL 33620 USA
[5] Stockholm Univ, Dept Struct Chem, S-10691 Stockholm, Sweden
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
SOLID-STATE NMR; 3-DIMENSIONAL LATTICE CONNECTIVITIES; AB-INITIO CALCULATIONS; C-13-C-13; J-COUPLINGS; BRONSTED ACID SITES; CRYSTAL-STRUCTURE; 1ST-PRINCIPLES CALCULATION; POWDER CRYSTALLOGRAPHY; ZEOLITE FRAMEWORKS; DIPOLAR COUPLINGS;
D O I
10.1021/ja311649m
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A general protocol is demonstrated for determining the structures of molecularly ordered but noncrystalline solids, which combines constraints provided by X-ray diffraction (XRD), one- and two-dimensional solid-state nuclear magnetic resonance (NMR) spectroscopy, and first-principles quantum chemical calculations. The approach is used to determine the structure(s) of a surfactant-directed layered silicate with short-range order in two dimensions but without long-range periodicity in three-dimensions (3D). The absence of long-range 3D molecular order and corresponding indexable XRD reflections precludes determination of a space group for this layered silicate. Nevertheless, by combining structural constraints obtained from solid-state Si-29 NMR analyses, including the types and relative populations of distinct Si-29 sites, their respective Si-29-O-Si-29 connectivities and separation distances, with unit cell parameters (though not space group symmetry) provided by XRD, a comprehensive search of candidate framework structures leads to the identification of a small number of candidate structures that are each compatible with all of the experimental data. Subsequent refinement of the candidate structures using density functional theory calculations allows their evaluation and identification of "best" framework representations, based on their respective lattice energies and quantitative comparisons between experimental and calculated Si-29 isotropic chemical shifts and (2)J(Si-29-O-Si-29) scalar couplings. The comprehensive analysis identifies three closely related and topologically equivalent framework configurations that are in close agreement with all experimental and theoretical structural constraints. The subtle differences among such similar structural models embody the complexity of the actual framework(s), which likely contain coexisting or subtle distributions of structural order that are intrinsic to the material.
引用
收藏
页码:5641 / 5655
页数:15
相关论文
共 117 条
[11]   Synthesis and characterization of the layered sodium silicate ilerite [J].
Brenn, U ;
Ernst, H ;
Freude, D ;
Herrmann, R ;
Jähnig, R ;
Karge, HG ;
Kärger, J ;
König, T ;
Mädler, B ;
Pingel, UT ;
Prochnow, D ;
Schwieger, W .
MICROPOROUS AND MESOPOROUS MATERIALS, 2000, 40 (1-3) :43-52
[12]   A structure refinement strategy for NMR crystallography:: An improved crystal structure of silica-ZSM-12 zeolite from 29Si chemical shift tensors [J].
Brouwer, Darren H. .
JOURNAL OF MAGNETIC RESONANCE, 2008, 194 (01) :136-146
[13]   Probing local structure in zeolite frameworks:: Ultrahigh-field NMR measurements and accurate first-principles calculations of zeolite 29Si magnetic shielding tensors [J].
Brouwer, Darren H. ;
Enright, Gary D. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (10) :3095-3105
[14]   NMR crystallography of zeolites:: Refinement of an NMR-solved crystal structure using ab initio calculations of 29Si chemical shift tensors [J].
Brouwer, Darren H. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (20) :6306-+
[15]   Structure solution of network materials by solid-state NMR without knowledge of the crystallographic space group [J].
Brouwer, Darren H. .
SOLID STATE NUCLEAR MAGNETIC RESONANCE, 2013, 51-52 :37-45
[16]   A solid-state NMR method for solution of zeolite crystal structures [J].
Brouwer, DH ;
Darton, RJ ;
Morris, RE ;
Levitt, MH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (29) :10365-10370
[17]   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
[18]   The 2D MAS NMR spin-echo experiment:: the determination of 13C-13C J couplings in a solid-state cellulose sample [J].
Brown, SP ;
Emsley, L .
JOURNAL OF MAGNETIC RESONANCE, 2004, 171 (01) :43-47
[19]   Determining hydrogen-bond strengths in the solid state by NMR:: the quantitative measurement of homonuclear J couplings [J].
Brown, SP ;
Pérez-Torralba, M ;
Sanz, D ;
Claramunt, RM ;
Emsley, L .
CHEMICAL COMMUNICATIONS, 2002, (17) :1852-1853
[20]   Advanced solid-state NMR methods for the elucidation of structure and dynamics of molecular, macromolecular, and supramolecular systems [J].
Brown, SP ;
Spiess, HW .
CHEMICAL REVIEWS, 2001, 101 (12) :4125-4155