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<title>Chemistry</title>
<link>http://hdl.handle.net/10468/178</link>
<description/>
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<rdf:li rdf:resource="http://hdl.handle.net/10468/946"/>
<rdf:li rdf:resource="http://hdl.handle.net/10468/992"/>
<rdf:li rdf:resource="http://hdl.handle.net/10468/922"/>
<rdf:li rdf:resource="http://hdl.handle.net/10468/993"/>
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<dc:date>2013-05-19T12:16:07Z</dc:date>
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<item rdf:about="http://hdl.handle.net/10468/946">
<title>Investigating the influence of the sulfur oxidation state on solid state</title>
<link>http://hdl.handle.net/10468/946</link>
<description>Investigating the influence of the sulfur oxidation state on solid state
Daly, Carla A.; Eccles, Kevin S.; Bateman, Lorraine M.; O'Boyle, Noel M.; Lawrence, Simon E.; Maguire, Anita R.
Design, synthesis and structural characterization of a series of diphenylacetylene derivatives bearing organosulfur, amide and amine moieties has been achieved in which the molecular conformation is controlled through variation of the hydrogen bond properties on alteration of the oxidisation level of sulfur.
</description>
<dc:date>2012-12-01T00:00:00Z</dc:date>
</item>
<item rdf:about="http://hdl.handle.net/10468/992">
<title>Nanostructured ferroelectric materials</title>
<link>http://hdl.handle.net/10468/992</link>
<description>Nanostructured ferroelectric materials
Varghese, Justin Manjaly
Nanostructured materials are central to the evolution of future electronics and&#13;
information technologies. Ferroelectrics have already been established as a&#13;
dominant branch in the electronics sector because of their diverse application range&#13;
such as ferroelectric memories, ferroelectric tunnel junctions, etc. The on-going&#13;
dimensional downscaling of materials to allow packing of increased numbers of&#13;
components onto integrated circuits provides the momentum for the evolution of&#13;
nanostructured ferroelectric materials and devices. Nanoscaling of ferroelectric&#13;
materials can result in a modification of their functionality, such as phase transition&#13;
temperature or Curie temperature (TC), domain dynamics, dielectric constant,&#13;
coercive field, spontaneous polarisation and piezoelectric response. Furthermore,&#13;
nanoscaling can be used to form high density arrays of monodomain ferroelectric&#13;
nanostructures, which is desirable for the miniaturisation of memory devices.&#13;
This thesis details the use of various types of nanostructuring approaches to fabricate&#13;
arrays of ferroelectric nanostructures, particularly non-oxide based systems. The&#13;
introductory chapter reviews some exemplary research breakthroughs in the&#13;
synthesis, characterisation and applications of nanoscale ferroelectric materials over&#13;
the last decade, with priority given to novel synthetic strategies. Chapter 2 provides&#13;
an overview of the experimental methods and characterisation tools used to produce&#13;
and probe the properties of nanostructured antimony sulphide (Sb2S3), antimony&#13;
sulpho iodide (SbSI) and lead titanate zirconate (PZT). In particular, Chapter 2&#13;
details the general principles of piezoresponse microscopy (PFM). Chapter 3&#13;
highlights the fabrication of arrays of Sb2S3 nanowires with variable diameters using&#13;
newly developed solventless template-based approach. A detailed account of&#13;
domain imaging and polarisation switching of these nanowire arrays is also&#13;
provided. Chapter 4 details the preparation of vertically aligned arrays of SbSI&#13;
nanorods and nanowires using a surface-roughness assisted vapour-phase deposition&#13;
method. The qualitative and quantitative nanoscale ferroelectric properties of these&#13;
nanostructures are also discussed. Chapter 5 highlights the fabrication of highly&#13;
ordered arrays of PZT nanodots using block copolymer self-assembled templates and&#13;
their ferroelectric characterisation using PFM. Chapter 6 summarises the&#13;
conclusions drawn from the results reported in chapters 3, 4 and 5 and the future&#13;
work.
</description>
<dc:date>2012-12-01T00:00:00Z</dc:date>
</item>
<item rdf:about="http://hdl.handle.net/10468/922">
<title>Accommodating curvature in a highly ordered functionalized metal oxide nanofiber: synthesis, characterization and multi-scale modeling of layered nanosheets</title>
<link>http://hdl.handle.net/10468/922</link>
<description>Accommodating curvature in a highly ordered functionalized metal oxide nanofiber: synthesis, characterization and multi-scale modeling of layered nanosheets
O'Dwyer, Colm; Gannon, G.; McNulty, D.; Buckley, D. Noel; Thompson, Damien
A key element in the rational design of hybrid organic-inorganic nanostructures, is control of surfactant packing and adsorption onto the inorganic phase in crystal growth and assembly. In layered single crystal nanofibers and bilayered 2D nanosheets of vanadium oxide, we show how the chemisorption of preferred densities of surfactant molecules can direct formation of ordered, curved layers. The atom-scale features of the structures are described using molecular dynamics simulations that quantify surfactant packing effects and confirm the preference for a density of 5 dodecanethiol molecules per 8 vanadium attachment sites in the synthesised structures. This assembly maintains a remarkably well ordered interlayer spacing, even when curved. The assemblies of interdigitated organic bilayers on V2O5 are shown to be sufficiently flexible to tolerate curvature while maintaining a constant interlayer distance without rupture, delamination or cleavage. The accommodation of curvature and invariant structural integrity points to a beneficial role for oxide-directed organic film packing effects in layered architectures such as stacked nanofibers and hybrid 2D nanosheet systems.
</description>
<dc:date>2012-10-01T00:00:00Z</dc:date>
</item>
<item rdf:about="http://hdl.handle.net/10468/993">
<title>Optimisation of chemoenzymatic processes in asymmetric synthesis</title>
<link>http://hdl.handle.net/10468/993</link>
<description>Optimisation of chemoenzymatic processes in asymmetric synthesis
Deasy, Rebecca E.
This thesis describes the optimisation of chemoenzymatic methods in asymmetric synthesis. Modern synthetic organic chemistry has experienced an enormous growth in biocatalytic methodologies; enzymatic transformations and whole cell bioconversions have become generally accepted synthetic tools for asymmetric synthesis. Biocatalysts are exceptional catalysts, combining broad substrate scope with high regio-, enantio- and chemoselectivities enabling the resolution of organic substrates with superb efficiency and selectivity. In this study three biocatalytic applications in enantioselective synthesis were explored and perhaps the most significant outcome of this work is the excellent enantioselectivity achieved through optimisation of reaction conditions improving the synthetic utility of the biotransformations.&#13;
In the first chapter a summary of literature discussing the stereochemical control of baker’s yeast (Saccharomyces Cerevisae) mediated reduction of ketones by the introduction of sulfur moieties is presented, and sets the work of Chapter 2 in context.&#13;
The focus of the second chapter was the synthesis and biocatalytic resolution of (±)-trans-2-benzenesulfonyl-3-n-butylcyclopentanone. For the first time the practical limitations of this resolution have been addressed providing synthetically useful quantities of enantiopure synthons for application in the total synthesis of both enantiomers of 4-methyloctanoic acid, the aggregation pheromone of the rhinoceros beetles of the genus Oryctes. The unique aspect of this enantioselective synthesis was the overall regio- and enantioselective introduction of the methyl group to the octanoic acid chain. This work is part of an ongoing research programme in our group focussed on baker’s yeast mediated kinetic resolution of 2-keto sulfones.&#13;
The third chapter describes hydrolase-catalysed kinetic resolutions leading to a series of 3-aryl alkanoic acids. Hydrolysis of the ethyl esters with a series of hydrolases was undertaken to identify biocatalysts that yield the corresponding acids in highly enantioenriched form. Contrary to literature reports where a complete disappearance of efficiency and, accordingly enantioselection, was described upon kinetic resolution of sterically demanding 3-arylalkanoic acids, the highest reported enantiopurities of these acids was achieved (up to &gt;98% ee) in this study through optimisation of reaction conditions. Steric and electronic effects on the efficiency and enantioselectivity of the biocatalytic transformation were also explored. Furthermore, a novel approach to determine the absolute stereochemistry of the enantiopure 3-aryl alkanoic acids was investigated through combination of co-crystallisation and X-ray diffraction linked with chiral HPLC analysis.&#13;
The fourth chapter was focused on the development of a biocatalytic protocol for the asymmetric Henry reaction. Efficient kinetic resolution in hydrolase-mediated transesterification of cis- and trans- β-nitrocyclohexanol derivatives was achieved. Combination of a base-catalysed intramolecular Henry reaction coupled with the hydrolase-mediated kinetic resolution with the view to selective acetylation of a single stereoisomer was investigated. While dynamic kinetic resolution in the intramolecular Henry was not achieved, significant progress in each of the individual elements was made and significantly the feasibility of this process has been demonstrated.&#13;
The final chapter contains the full experimental details, including spectroscopic and analytical data of all compounds synthesised in this project, while details of chiral HPLC analysis are included in the appendix. The data for the crystal structures are contained in the attached CD.
</description>
<dc:date>2012-09-01T00:00:00Z</dc:date>
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