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Brian W. Skelton

Researcher at University of Western Australia

Publications -  1662
Citations -  33374

Brian W. Skelton is an academic researcher from University of Western Australia. The author has contributed to research in topics: Crystal structure & Ligand. The author has an hindex of 69, co-authored 1646 publications receiving 31889 citations. Previous affiliations of Brian W. Skelton include Monash University, Clayton campus & State University of Malang.

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Structural and stereochemical correlations of polypropionate metabolites from marine pulmonates: revision of the relative stereochemistry of pectinatone by X-ray structure analysis

TL;DR: In this article, the relative stereochemistry of pectinatone was revised to (14) by X-ray diffraction analysis, which revealed two major stereochemical types: polypropionate metabolites isolated from marine pulmonates of the genus Siphonaria.
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Cluster control in oligouranyl complexes of p-t-butylcalix[8]arene

TL;DR: In all, the calixarene hexa-anion is present in a virtually identical conformation, suggesting that conformational preferences of the ligand must be a major factor controlling the form of the bound oxo-metal complex.
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Lewis-base adducts of lead(II) complexes. Part 6. X-Ray structural characterisation of adducts of lead(II) bis(perchlorate) with dimethyl sulfoxide

TL;DR: In this article, the lead-II perchlorate (PbO2Pb) was analyzed as a 1:6 adduct and the structure was refined to a residual of 0.055 for 3526 independent observations.
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Synthesis and structure of alkynylplatinum(IV) complexes containing the pincer group [2,6-(dimethylaminomethyl)phenyl-N, C, N]-

TL;DR: In this article, the pincer group is present as a tridentate donor and the alkynyl group is located cis to pincers carbon donor, and the triflate (1a, 1b) and iodide groups (2a, 2b) are located trans-to pincher carbon; an X-ray structural analysis was completed for 2b.
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Coordinating Tectons: Bimetallic Complexes from Bipyridyl Terminated Group 8 Alkynyl Complexes

TL;DR: In this paper, a range of binuclear and heterometallic ruthenium-alkynyl complexes have been shown to undergo reversible one-electron oxidations centered on the alkynyl ligands, as has been observed previously for closely related complexes.