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Paul A Wright

Publications and source records attributed to Paul A Wright.

14 recordsLinked to original sources

Complex zeolite structure solved by combining powder diffraction and electron microscopy.

Many industrially important materials, ranging from ceramics to catalysts to pharmaceuticals, are polycrystalline and cannot be grown as single crystals. This means that non-conventional methods of structure analysis must be applied to obtain the structural information that is fundamental to the understanding of the properties of these materials. Electron microscopy might appear to be a natural approach, but only relatively simple structures have been solved by this route. Powder diffraction is another obvious option, but the overlap of reflections with similar diffraction angles causes an ambiguity in the relative intensities of those reflections. Various ways of overcoming or circumventing this problem have been developed, and several of these involve incorporating chemical information into the structure determination process. For complex zeolite structures, the FOCUS algorithm has proved to be effective. Because it operates in both real and reciprocal space, phase information obtained from high-resolution transmission electron microscopy images can be incorporated directly into this algorithm in a simple way. Here we show that by doing so, the complexity limit can be extended much further. The power of this approach has been demonstrated with the solution of the structure of the zeolite TNU-9 (|H9.3|[Al9.3Si182.7O384]; ref. 10) with 24 topologically distinct (Si,Al) atoms and 52 such O atoms. For comparison, ITQ-22 (ref. 11), the most complex zeolite known to date, has 16 topologically distinct (Si,Ge) atoms.

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The first route to large pore metal phosphonates.

The first large pore (free diameter > 7 A) metal phosphonates have been prepared as divalent metal N,N'-piperazinebis(methylenephosphonate)s that possess pores greater than ca. 10 A in free diameter, are stable up to 400 degrees C and offer a route to chiral adsorbents and catalysts.

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Generation of atomistic models of periodic mesoporous silica by kinetic Monte Carlo simulation of the synthesis of the material.

We have developed a molecular simulation method for the generation of realistic atomic-level models for periodic mesoporous silicas. Using simplified interaction potentials and simplified representations of the templating micelles, the simulation follows the reaction path of the hydrothermal synthesis and calcination of the silica material in a kinetic Monte Carlo (kMC) simulation. The only input to the simulation is the geometry of the micelle and the number of silicic acid monomers at the beginning of the synthesis. We simulated the adsorption properties of the PMS models using Grand Canonical Monte Carlo simulation. With use of MCM-41 materials of different pore sizes as a prototype material, experimental and simulated adsorption isotherms for nitrogen, ethane, and carbon dioxide were compared, showing good agreement between simulation and experiment.

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Motion of aromatic hydrocarbons in the microporous aluminum methylphosphonates AlMePO-alpha and AlMePO-beta.

(2)H wide-line NMR has been used, in conjunction with molecular dynamics simulations where appropriate, to follow the reorientation of the monoaromatic compounds benzene, toluene, and p-xylene within the one-dimensional channels of the alpha- and beta-polymorphs of aluminum methylphosphonate, Al(2)(CH(3)PO(3))(3). Variable-temperature, static, (2)H NMR spectra of adsorbed d(6)-benzene, d(3)-, d(5)-, and d(8)-toluenes, and d(3),d(3)-p-xylene were matched by line shape simulation. The motion of p-xylene in both polymorphs is approximated by the long axis of the molecule describing a cone within the channels, the half-angle of which is greater for the slightly wider channels in AlMePO-beta (27-30 degrees cf. 18-19 degrees). The (2)H NMR of d(3)-toluene is simulated using a similar model, whereas the signal from aromatic deuterons in d(5)- and d(8)-toluenes is simulated by a ring undergoing 2pi/3 flips around the para axis. The reorientation of benzene shows the largest differences between the two pore structures. In AlMePO-beta it tumbles with little restriction, although at low temperatures the spectral details are better matched by allowing the molecule to spend a greater proportion of its time closer to the wall. In AlMePO-alpha the much broader line shape arises from constrained motion within the strongly triangular channels. Molecular dynamics simulations of benzene in the two structures confirm the differences. They support a model for benzene in AlMePO-alpha where its motion is restricted to rotations about its 6-fold axis and 2pi/3 jumps between symmetry-related sites in the pores, so that the plane of the aromatic ring remains approximately parallel to the c-axis.

Aluminum↗

Synthesis and structure of the framework scandium methylphosphonates ScF(H2O)CH3PO3 and NaSc(CH3PO3)2.0.5H2O.

Two framework scandium methylphosphonates have been prepared hydrothermally and their structures solved. ScF(H(2)O)CH(3)PO(3) is a non-porous solid built up from -ScF- chains linked by methylphosphonate groups. The ScO(4)F(2) octahedra are completed by a coordinated water molecule. NaSc(CH(3)PO(3))(2).0.5H(2)O was solved ab initio from high-resolution synchrotron X-ray powder diffraction data. It has a fully connected, negatively charged scandium phosphonate framework where ScO(6) octahedra share vertices with PO(3)CH(3) groups. The solid contains charge balancing sodium cations, coordinated by a water molecule, which may be reversibly removed and adsorbed. The structure of the perdeuterated, dehydrated solid has been refined against neutron powder diffraction data collected at 2.5 K, showing the CD(3) groups in a fully staggered orientation with respect to the phosphonate oxygen atoms.

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The pH-controlled hydrothermal synthesis and crystal structures of two zinc N,N'-piperazinebis(methylenephosphonate) frameworks.

An exploration of the reactions of N,N'-piperazinebis(methylenephosphonic acid), H4L, with zinc salts has led to the isolation of two new framework zinc phosphonates. ZnLH2.H2O (I) is isostructural with previously reported manganese(II) and cobalt(II) analogues, and consists of infinite 'zinc phosphate' chains bridged into three dimensions via the organic moieties. The resulting framework encloses large channels in which the loosely bound H2O resides. The H2O is lost reversibly at around 160 degree C, without framework collapse. Zn2L (II) has a novel framework structure, prepared at an initial pH > 7, which consists of two-dimensional 'zinc phosphate' sheets, comprising both four- and eight-membered -Zn-O-P- rings, which are also linked into three dimensions via the organic groups. In both cases, the zinc centre is tetrahedral; in I coordination is by oxygen atoms from four different phosphonate groups, whereas in II the additional deprotonation of the ligand allows coordination via three oxygen atoms plus the amine nitrogen atom.

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Two closely related lanthanum phosphonate frameworks formed by anion-directed linking of inorganic chains.

Two novel three-dimensional lanthanum coordination polymers have been prepared with the phosphonic acid H2O3PCH2N(C2H4)2 NCH2PO3H2 (LH4). La2(LH2)2(LH4)Cl2 (I) and La2(LH2)2(LH3)Cl (II) arise from similar hydrothermal reactions but differing sources of La. A one-dimensional "lanthanum-phosphate" chain, comprising corner-linked LaO7 and PO3C polyhedra, forms the basis for the two different structures. The two structures differ in the mode of connectivity of the inorganic chains via the phosphonate groups. Both materials include extraframework chloride ions, the different amounts of which apparently direct the polytypic structures. In II, the chloride ions are incorporated in a noncentrosymmetric manner leading to a polar framework topology.

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Direct observation of growth defects in zeolite beta.

High-resolution transmission electron microscopy reveals linear, "double pore" defects in the important zeolite beta. Structural interpretation of these defects gives evidence for the mechanism by which the zeolite crystallizes.

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Structure of the mesoporous silica SBA-2, determined by a percolation analysis of adsorption.

We have carried out a percolation analysis of the adsorption of ethane and nitrogen in SBA-2, a structured mesoporous silica consisting of a hexagonal close-packed (hcp) array of spherical cavities connected by cylindrical channels. Our analysis explains the different uptakes of nitrogen and ethane in terms of the greater accessibility of the network to the smaller nitrogen molecule. The analysis also allows us to quantify the connectivity of the SBA-2 pore network. The effective coordination number of the cavities, defined as the average number of channels per cavity that are large enough to allow nitrogen to pass, is 4.9, much less than the theoretical maximum value of 12. Taking into account only the smaller set of channels large enough to admit ethane, the effective coordination number is 1.8, just above the percolation threshold of the network.

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Elucidation of the pore structure of SBA-2 using Monte Carlo simulation to interpret experimental data for the adsorption of light hydrocarbons.

We have measured the adsorption of methane and ethane to high pressure on SBA-2, a structured mesoporous silica composed of spheres connected by narrow channels. The experimental data were analyzed by carrying out Monte Carlo simulations of adsorption in pore structure models of different complexity and then adjusting the parameters of the models to match the Monte Carlo results to the experimental data. We found that a model based on single-sized spherical cavities was inadequate and that it is necessary to explicitly account for the interconnecting channels. Further, we found that despite the basic regularity of the SBA-2 structure, it is necessary to allow for a distribution of the sizes of both the cavities and the channels. These size distributions were obtained by fitting the parameters of the model to the experimental adsorption data, revealing detailed structural information not previously known for this material. The channels were found to be 5-15 A in diameter, while the cavities were 40-50 A in diameter. There is some evidence that the distribution of channel sizes leads to a percolation effect whereby the pore structure is not equally accessible to all adsorptives.

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Synthesis, structure solution, characterization, and catalytic properties of TNU-10: a high-silica zeolite with the STI topology.

A high-silica zeolite (Si/Al = 7.1) with the STI framework topology, denoted TNU-10, has been synthesized in the presence of 1,4-bis(N-methylpyrrolidinium)butane and Na(+) cations as structure-directing agents, and its structure in the proton form has been refined against laboratory powder X-ray data in space group Fmmm (a = 13.533(1) A, b = 17.925(2) A, c = 17.651(2) A). The space group symmetry is supported by electron diffraction and energy minimization studies. The as-made and proton form of TNU-10 are extensively characterized by elemental and thermal analyses, scanning electron microscopy, N(2) adsorption, multinuclear solid-state NMR, IR, and temperature-programmed desorption of ammonia, and the location of the organic structure-directing agent in the channel system is determined by molecular modeling. The catalytic properties of H-TNU-10 and Co-TNU-10 are evaluated for the skeletal isomerization of 1-butene to isobutene and the selective reduction of NO with methane, respectively. When compared to H-ferrierite, a low selectivity to isobutene is observed for H-TNU-10. However, it is found that Co-TNU-10 exhibits a maximum NO conversion of 93% at 823 K under conditions of high concentrations of methane (16,000 ppm) and water vapor (10%) and in the presence of 2.6% O(2), which is considerable higher than even the value (74%) obtained from Co-ferrierite, known as the best catalyst for this reaction, under the identical conditions.

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Structure solution of a novel aluminium methylphosphonate using a new simulated annealing program and powder X-ray diffraction data.

The structure of a novel layered aluminium methylphosphonate, formula Al2(CH3PO3)3, has been solved from laboratory X-ray powder diffraction data by simulated annealing of five independent structural sub-units, revealing a combination of four- and five-fold coordinated aluminiums within the inorganic lamellae that is unique for this kind of solid.

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