P
Peter S. White
Researcher at University of North Carolina at Chapel Hill
Publications - 641
Citations - 36290
Peter S. White is an academic researcher from University of North Carolina at Chapel Hill. The author has contributed to research in topics: Crystal structure & Ligand. The author has an hindex of 72, co-authored 637 publications receiving 34509 citations. Previous affiliations of Peter S. White include National Park Service & University of Chicago.
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Nativity and seed dispersal mode influence species’ responses to habitat connectivity and urban environments
TL;DR: It is demonstrated that urbanization influences plant species composition via its effects on both habitat connectivity and environmental conditions, however, the strength of these effects varies somewhat predictably across seed dispersal modes and between native and exotic species.
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Electrophilic behaviour of nitrosyls: the Boedeker reaction, the reactions of sulphite with nitrosyls, and the crystal and molecular structure of cis-bis(2,2′-bipyridine)chloro(nitrosylsulphito)ruthenium
TL;DR: In this paper, the structure of cis-[RuCl(bipy)2{N(O)SO3}] has been determined by X-ray diffraction and it is best regarded as a ruthenium(II) complex containing the hitherto unknown ligand [ONSO3] which is N-coordinated to RuII.
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Reactions of phenylaluminium compounds with E(SiMe3)3 (E = P or AS): X-ray crystal structures of Ph3Al·E(SiMe3)3 (E = P or As) and Ph2(Cl)Al·P(SiMe3)3
TL;DR: In this paper, the dehalosilylation reactions between Ph 2 AlCl and E(SiMe 3 ) 3 (E = P or As) in 1:1 mole ratios yielded only the adducts Ph 2 (Cl)Al·E(SiME 3 )3 [E = p( III ) and As( IV )].
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The preparation and crystal structure of 5SbF3•3SbF5
TL;DR: In this article, a single-crystal X-ray diffraction study of SbF3·SbF5 was performed and the structure was refined to a final R of 0.057 for 3 718 reflections.
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Electrophilic behaviour of nitrosyls: the reactions of ketones with nitrosyls and the crystal and molecular structure of the product of the reaction between trans-chloro(nitrosyl)tetra(pyridine)ruthenium and acetone
TL;DR: In this paper, the PF6− salt was characterized by i.m.r and n.r. spectroscopies and by X-ray diffraction, and it was shown that the predominant tautomer in the ligand is the delocalised form N([graphic omitted])CH3.