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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 Spectroscopic Studies of Halocuprate(I) and Haloargentate(I) Complexes [M2XnX′4−n]2−

TL;DR: In this paper, the properties of the bis(triphenylphosphoranylidene)ammonium (Ph3PNPPh3]- = PNP+) complexes were characterized by single crystal structural determinations.
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The Alkaloids of Ophiorrhiza cf. ferruginea

TL;DR: In this paper, the aerial parts of Ophiorrhiza cf. ferruginea (Rubiaceae) have been extracted and the tertiary indole alkaloids dihydrocycloakagerine (1), 3,14-dihydrodecussine (mostuenine) (3) and tetrahydroakagerine(4), and the quaternary indole acid isomalindine (5) are confirmed by the X-ray method.
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Cu/Cd heterometallic solids with the [Cu(Hdea)(H2dea)]22+ motif (H2dea = diethanolamine): Exchange interactions through hydrogen bonding

TL;DR: The hybrid composites [Cu(Hdea)(H2dea)]2[CdX4], X=Br (1), I (2) have been prepared in reactions of zero-valent copper with cadmium halide in air-exposed solution containing the corresponding ammonium salt and diethanolamine (H 2dea), and X-ray crystallographic analysis reveals ionic solids of non-symmetric H-bonded dimeric [ Cu ( Hdea ) ( H 2 dea ) ] 2 2 +
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NMR spectroscopy, x-ray crystallographic, and molecular modeling studies on a new pyranone from Haloxylon salicornicum

TL;DR: A new pyranone, 5-hydroxy-3-methoxy-4H-pyran-4-one, was isolated from the aerial parts of the desert shrub Haloxylon salicornicum by X-ray structural analysis, NMR spectroscopy, and mass spectrometry.
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Coordination and Rearrangement of Organic Chalcogenides on a Rhodium-Rhodium Bond: Reactions with Strained-Ring Cyclic Thioethers and with Selenium and Tellurium Ligands

TL;DR: When the cyclic thioethers were added to [(η5-C5H5)2Rh2(CO)(μ-η1:η2-CF3C2CF3)L] (2a−c) were formed reversibly as mentioned in this paper.