Radom is the leading practitioner in Australia, and one of the leaders internationally, in the application of molecular orbital theory to structure and mechanism in organic chemistry. His particular emphasis is on the structures and stabilities of species on which experiments are difficult (reactive intermediates, unstable molecules) or almost impossible (transition states). The wide acceptance of his term distonic for a class of radical cation intermediates follows his recent work showing that gas­phase radical cations with charge and radical sites on different atoms often display a stability which contrasts with that of their neutral parents. Radom's predictions preceded the now numerous observations of distonic radical cations.

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Hans Freeman is largely known for his numerous contributions to the structures and chemistry of transition metal complexes of amino acids and peptides. He is regarded as a world authority in this area and his work is widely quoted and used. This background has culminated more recently in the solution of the structure of the Copper protein plastocyanin, one of the proteins in the photosynthetic system. The structural analysis of the cupric form was a decisive experiment and it resolved some spectroscopic and redox anomalies of the entire class of "blue" copper proteins. The subsequent refinement at high resolution and the pH dependence of the structure of the reduced form have provided an important insight into the function of plastocyanin in photosynthesis.

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J. N. Israelachvili has made key contributions to experimental surface science and to theoretical membrane biology. Work with his unique apparatus, which measures forces between surfaces immersed in liquids with distance resolution of 1 Ångstrom, has not simply confirmed modern theories, but has revealed a hierarchy of new forces due to liquid structure at interfaces at distances below 50 Å separation. These forces are essential to an understanding of a wide variety of phenomena in industry and nature. Israelachvili also pioneered the theory of self-assembly of surfactant, liquid and protein molecules into structures like micelles, vesicles and membranes, bringing order to a broad field there.

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Bennett is distinguished for his sustained and original contributions in the field of organo-metallic chemistry. He is well known internationally for his work on the activation of organic and inorganic molecules by organo-transition metal complexes which has been definitive and leads directly to a better understanding of heterogeneous catalysis, especially in its application to the petrochemical industry. His imaginative studies range widely and include the formation of metal-carbon σ-bonds in oxidative additions, cyclo-metallation reactions with bidentate tertiary phosphines, the stabilization of short-lived organic molecules of transition metal centres, and the activation of aromatic hydrocarbons by arene complexes of ruthenium. He was awarded the H.G. Smith Medal of the Royal Australian Chemical Institute in 1977.

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Hush has contributed to chemical physics and theoretical chemistry. His Theory of homogenous and heterogenous electron transfer as a thermal rate process has become generally accepted. Later he identified a radiative process in electron transfer, and investigated a number of key examples. His theoretical work has been in the use of self-consistent field molecular orbital theory in electron transfer problems, particularily in the electron transfer systems of certain tetrapyrrole macrocyclics and their metal complexes. The combination of ingenious experimentation and convincing theoretical interpretation is a feature of his work, which has been notably original, and is in areas of real importance.

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Sargeson is distinguished for his sustained and original contributions to elucidating the mechanisms of inorganic reactions. His studies during the past 10-15 years have been central in raising inorganic synthesis from the doldrums of random ad hoc procedures by the disciplined and systematic application of fundamental mechanistic principles. His work on the mechanism of the base hydrolysis reactions of cobalt (III) has been definitive and leads directly to a new and deeper understanding of the likely mechanisms for reactions such as amino acid ester and peptide hydrolysis in carboxypeptidase A. He was among the first to appreciate the significance of the chiral coordinated amine centre for integrating synthesis with stereochemistry and mechanism through configurational relationships between reactant and product. His ensuing applications of inorganic conformational analysis to chemical and biological specificity have been pioneering. He is an international authority in his field.

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Craig developed experimental and theoretical methods for the interpretation of the spectra of molecular crystals which are now the bases of widely used procedures. He worked out the theory of second-order crystalline interactions in molecular crystals and made the first quantitative calculations of exciton energies in a molecular crystal. In valence theory he demonstrated the importance of configuration interaction for π-electrons in aromatic molecules. His early papers on this subject and one written in collaboration with R.G. Parr and I.G. Ross have become standard references in the field. He has also contributed to knowledge of aromatic character, especially in cyclic inorganic systems such as phosphonitrilic halides.

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Dr. Ninham's early work was in Statistical Mechanics and in this field he made significant contributions to the theory of phase transitions, to the Ising model, and to the theory of distribution functions. Ninham has been remarkable for the range of his interests, his inventiveness, and his originality in entering new fields and making significant contributions to these fields. His recent work on the calculation of Van der Waals forces in biological materials is considered a major advance in the understanding of cell biological phenomena.

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Dr. Barker has made major contributions to our knowledge of solutions and dense vapours by his work on the statistical mechanics of molecular interactions, especially of polar molecules. His studies of the effects of correlation between the motions of adjacent molecules have led to his important new "tunnel theory" of liquids, which in many respects constitutes a marked advance on previous "cell" theories. He has also done high-quality experimental work on alcohol solutions, and has contributed to the study of diffusion in graphite, counter-current distribution in liquids, and critical solution phenomena.

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Karl Glazebrook is a world-leading astronomer whose research has led to major advances in our understanding of how galaxies and the Universe evolve over time. His ground-breaking work includes, establishing the existence of massive galaxies only three billion years after the Big Bang, and discovering the local analogues of primordial galaxies. Glazebrook has also pioneered near-infrared surveys and developed new award-winning instrumental techniques for carrying out ultra-deep spectroscopic surveys on the world’s largest telescopes. He has also been at the vanguard in the application of new observational techniques for quantifying the effects of dark energy on the accelerating expansion of the Universe.

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