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John Meurig Thomas

Publications and source records attributed to John Meurig Thomas.

At least 19 recordsLinked to original sources
PubMed2006

Single-site photocatalytic solids for the decomposition of undesirable molecules.

Photocatalytic solids, in which the absorption occurs at isolated, spatially well-separated centres, are particularly useful catalysts for effecting reactions that are of prime importance in both remedial and preparative contexts. These are qualities that they share with single-site (thermally-activated) heterogeneous catalysts; but they have the added advantage of being more readily probed during the actual processes of catalytic turnover, since they generally function under ambient conditions, unlike most conventional solid catalysts which usually operate at elevated pressures and temperatures. Thus, they are amenable to investigation by (in situ) X-ray absorption (XAFS), FT-IR, UV-Vis, and EPR spectroscopic studies as well as to photoluminescence measurement. This affords greater insight into the mechanisms of the photocatalytic reactions as we illustrate in this short review. Open-structure solids such as mesoporous silica and zeolitic aluminosilicates offer a generally applicable strategy to design new single-site photocatalysts such as those described here for the decomposition of NO to N2 and O2 and for the selective oxidation of CO in the presence of H2.

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PubMed2006

Improved CO oxidation activity in the presence and absence of hydrogen over cluster-derived PtFe/SiO2 catalysts.

The catalytic performance of cluster-derived PtFe/SiO(2) bimetallic catalysts for the oxidation of CO has been examined in the absence and presence of H(2) (PROX) and compared to that of Pt/SiO(2). PtFe(2)/SiO(2) and Pt(5)Fe(2)/SiO(2) samples were prepared from PtFe(2)(COD)(CO)(8) and Pt(5)Fe(2)(COD)(2)(CO)(12) organometallic cluster precursors, respectively. FTIR data indicate that both clusters can be deposited intact on the SiO(2) support. The clusters remained weakly bonded to the SiO(2) surface and could be extracted with CH(2)Cl(2) without any significant changes in their structure. Subsequent heating in H(2) led to complete decarbonylation of the supported clusters at approximately 350 degrees C and the formation of Pt-Fe nanoparticles with sizes in the 1-2 nm range, as indicated by HRTEM imaging. A few larger nanoparticles enriched in Pt were also observed, indicating that a small fraction of the deposited clusters were segregated to the individual components following the hydrogen treatment. A higher degree of metal dispersion and more homogeneous mixing of the two metals were observed during HRTEM/XEDS analysis with the cluster-derived samples, as compared to a PtFe/SiO(2) catalyst prepared through a conventional impregnation route. Furthermore, the cluster-derived PtFe(2)/SiO(2) and Pt(5)Fe(2)/SiO(2) samples were more active than Pt/SiO(2) and the conventionally prepared PtFe/SiO(2) sample for the oxidation of CO in air. However, substantial deactivation was also observed, indicating that the properties of the Pt-Fe bimetallic sites in the cluster-derived samples were altered by exposure to the reactants. The Pt(5)Fe(2)/SiO(2) sample was also more active than Pt/SiO(2) for PROX with a selectivity of approximately 92% at 50 degrees C. In this case, the deactivation with time on stream was substantially slower, indicating that the highly reducing environment under the PROX conditions helps maintain the properties of the active Pt-Fe bimetallic sites.

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PubMed2006

Highly efficient one-step conversion of cyclohexane to adipic acid using single-site heterogeneous catalysts.

A solid source of 'active' oxygen (acetylperoxyborate, APB), when dissolved in aqueous solution in the presence of a single-site microporous catalyst containing redox centres (Fe(III)AlPO-31, Mn(III)AlPO-5, Fe(III)AlPO-5), converts cyclohexane with high efficiency (ca. 88%) and exceptionally high selectivity (ca. 81%) to adipic acid at 383 K; this procedure is also effective in converting styrene to styrene oxide and -pinene and (+)-limonene to their corresponding epoxides.

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PubMed2005

Direct visualisation, by aberration-corrected electron microscopy, of the crystallisation of bimetallic nanoparticle catalysts.

Using a scanning transmission electron microscope, corrected for aberration, ultra-high resolution images of the internal structure of nanoparticle clusters, as well as the number of atoms present per cluster, may be directly determined: it is shown that individual bimetallic clusters of Ru10Pt2 have a "molecular" structure and that when they coalesce into larger entities containing ca. 200 atoms they adopt the regular crystalline, and facetted, state of a bulk metal.

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PubMed2005

Single-site heterogeneous catalysts.

Intellectually, the advantages that flow from the availability of single-site heterogeneous catalysts (SSHC) are many. They facilitate the determination of the kinetics and mechanism of catalytic turnover-both experimentally and computationally-and make accessible the energetics of various intermediates (including short-lived transition states). These facts in turn offer a rational strategic principle for the design of new catalysts and the improvement of existing ones. It is generally possible to prepare soluble molecular fragments that circumscribe the single-site, thus enabling a direct comparison to be made, experimentally, between the catalytic performance of the same active site when functioning as a heterogeneous (continuous solid) as well as a homogeneous (dispersed molecular) catalyst. This approach also makes it possible to modify the immediate atomic environment as well as the central atomic structure of the active site. From the practical standpoint, SSHC exhibit very high selectivities leading to the production of sharply defined molecular products, just as do their homogeneous analogues. Given that mesoporous silicas with very large internal surface areas are ideal supports for SSHC, and that more than a quarter of the elements of the Periodic Table may be grafted as active sites onto such silicas, there is abundant scope for creating new catalytic opportunities.

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PubMed2005

Design of a "green" one-step catalytic production of epsilon-caprolactam (precursor of nylon-6).

The ever-increasing industrial demand for nylon-6 (polycaprolactam) necessitates the development of environmentally benign methods of producing its precursor, epsilon-caprolactam, from cyclohexanone. It is currently manufactured in two popular double-step processes, each of which uses highly aggressive reagents, and each generates substantial quantities of largely unwanted ammonium sulfate as by-product. Here we describe a viable laboratory-scale, single-step, solvent-free process of producing epsilon-caprolactam using a family of designed bifunctional, heterogeneous, nanoporous catalysts containing isolated acidic and redox sites, which smoothly convert cyclohexanone to epsilon-caprolactam with selectivities in the range 65-78% in air and ammonia at 80 degrees C. The catalysts are microporous (pore diameter 7.3 A) aluminophosphates in which small fractions of the Al(III)O4(5-) and P(V)O4(3-) tetrahedra constituting the 4-connected open framework are replaced by Co(III)PO4(5-) and Si(IV)O4(4-) tetrahedra, which become the loci of the redox and acidic centers, respectively. The catalysts may be further optimized, and already may be so designed as to generate selectivities of approximately 80% for the intermediate oxime, formed from NH2OH, which is produced in situ within the pore system. The advantages of such designed heterogeneous catalysts, and their application to a range of other chemical conversions, are also adumbrated.

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PubMed2005

Catalysis: principles, progress, prospects.

In this introductory paper, we endeavour to bridge the gaps that currently exist between the three main subdivisions of catalysis: enzymatic, homogeneous and heterogeneous. Hitherto, there has been a tendency for each of these three divisions to grow separately using their own concepts, phrases and techniques. However, there is much that unites them, not least the notion of the catalytically active site and, in particular, its often unusual (constrained) state of electronic or atomic environmental disposition. We identify many points of similarity between, for example, the mode of action of, metalloenzymes on the one hand and the recent generation of transition metal ions embedded within nanoporous (usually siliceous) solids on the other. Useful unifying principles emerge from considerations of free-energy/reaction-coordinate plots. We present a number of tabulations and comparisons designed to facilitate the understanding of the mode of operation of existing, and the performance of new, catalysts. In doing so, we have drawn on our own work as well as that of others, including contributions that are to be found in this volume, with the intention of covering the great variety of catalytic phenomena.

Catalysis↗
PubMed2004

High-resolution transmission electron microscopy: the ultimate nanoanalytical technique.

To be able to determine the elemental composition and morphology of individual nanoparticles consisting of no more than a dozen or so atoms that weigh a few zeptograms (10(-21) g) is but one of the attainments of modern electron microscopy. With slightly larger specimens (embracing a few unit cells of the structure) their symmetry, crystallographic phase, unit-cell dimension, chemical composition and often the valence state (from parallel electron spectroscopic measurements) of the constituent atoms may also be determined using a scanning beam of electrons of ca. 0.5 nm diameter. Nowadays electron crystallography, which treats the digital data of electron diffraction (ED) and high-resolution transmission electron microscope (HRTEM) images of minute (ca. 10(-18)g) specimens in a quantitatively rigorous manner, solves hitherto unknown structures just as X-ray diffraction does with bulk single crystals. In addition, electron tomography (see cover photograph and its animation) enables a three-dimensional picture of the internal structure of minute objects, such as nanocatalysts in a single pore, as well as structural faults such as micro-fissures, to be constructed with a resolution of 1 nm from an angular series of two-dimensional (projected) images. Very recently (since this article was first written) a new meaning has been given to electron crystallography as a result of the spatio-temporal resolution of surface phenomena achieved on a femtosecond timescale.

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PubMed2003

Constraining asymmetric organometallic catalysts within mesoporous supports boosts their enantioselectivity.

By constraining tethered asymmetric organometallic catalysts within the nanopores of silica supports so as to increase the interaction between the pore wall and the active center (and hence to restrict access of the reactant to the catalyst), a significant improvement in enantioselectivity is achieved. A schematic illustration of a cationic chiral, organometallic catalyst, [Rh(I)(COD)PMP] {(S)-(+)-1-(2-pyrrolidinylmethyl)-pyrrolidine and cyclooctadiene}, which is noncovalently anchored via a N-H...F hydrogen bond with the triflate ion, CF3SO3-, to the curved inner surface of a 38 A diameter pore of a silica support for the asymmetric hydrogenation of the C=O bond in methyl benzoylformate to the corresponding methyl mandelate is shown. Rh (purple); N (blue); H (white); F (green); C (gray); S (yellow); O (red).

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