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James Alexis Platts

Researcher at Cardiff University

Publications -  241
Citations -  7776

James Alexis Platts is an academic researcher from Cardiff University. The author has contributed to research in topics: Hydrogen bond & Density functional theory. The author has an hindex of 42, co-authored 231 publications receiving 7152 citations. Previous affiliations of James Alexis Platts include University of South Australia & Aarhus University.

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Experimental and theoretical charge density distribution in two ternary cobalt(III) complexes of aromatic amino acids.

TL;DR: The transferability between isomers of the charge density and derived parameters is investigated and found to be invalid for these structurally related systems.
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A putative bioactive conformation for the altered peptide ligand of myelin basic protein and inhibitor of experimental autoimmune encephalomyelitis [Arg91, Ala96] MBP87–99

TL;DR: NMR experiments coupled with theoretical calculations are found to be in agreement with X-ray crystallography data and open an avenue for the design and synthesis of novel peptide restricted analogues as well as peptide mimetics that rises as an ultimate goal.
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Experimental and theoretical charge-density study of a tetranuclear cobalt carbonyl complex.

TL;DR: Details of the complex bonding environment present in the molecular centre of an alkyne-bridged dicobalt complex have been examined using a combination of experimental and theoretical charge-density modelling for two compounds which share a central Co( 2)C(2) tetrahedral moiety as their common motif.
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Quaternary Ammonium Arylspiroborate Esters as Organo-Soluble, Environmentally Benign Wood Protectants

TL;DR: In this article, three related tetra-n-butylammonium spiroborates and four related borates have been examined for leach resistant wood preservatives, the anti-fungal and termiticidal activities, and the resistance to leaching from timber.
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A facile regioselective 1,3-dipolar cycloaddition protocol for the synthesis of new class of quinolinyl dispiro heterocycles

TL;DR: In this paper, the 1,3-dipolar cycloaddition reaction of azomethine ylides generated in situ from isatin and secondary amino acids with quinolinyl dipolarophiles in refluxing methanol afforded new class of quinoline dispiro heterocycles with multi hetero core units.