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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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Correlation and prediction of critical micelle concentration using polar surface area and LFER methods

TL;DR: In this article, the linear free energy relationship of Abraham and a modified polar surface area approach were used to calculate critical micelle concentration (CMC) for anionic, non-ionic and structurally diverse molecules, including many commercially important drugs such as analgesics, anaesthetic and antibiotics.
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Tuning the Electronics of Phosphorescent, Amide‐Functionalized, Cyclometalated IrIII Complexes: Syntheses, Structures, Spectroscopy and Theoretical Studies

TL;DR: In this paper, single crystal X-ray diffraction studies were undertaken on two Iridium(III) complexes, which showed that each adopts a distorted octahedral coordination geometry with retention of the expected trans-N, cis-C arrangement of the cyclometalated ligands.
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Aryl azide photochemistry in defined protein environments.

TL;DR: A genetically encoded precursor to an aryl nitrene, para-azidophenylalanine, was introduced site specifically into proteins to deduce if distinct environments were capable of caging a reactive organic intermediate.
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A combined NMR and molecular dynamics simulation study to determine the conformational properties of agonists and antagonists against experimental autoimmune encephalomyelitis.

TL;DR: A robust method, which is based on a combination of molecular dynamics and energy minimization, is proposed for identifying the putative bioactive conformations of the EAE inducing epitope MBP and the structural motif for the agonist-antagonist activity is discussed.
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Design and Synthesis of Non-Peptide Mimetics Mapping the Immunodominant Myelin Basic Protein (MBP83-96) Epitope to Function as T-Cell Receptor Antagonists.

TL;DR: These studies show that lead compounds 15 and 16 may be used for immunotherapy against MS and are able to inhibit to some extent the stimulation of T cells by the immunodominant MBP83–99 peptide from immunized mice.