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Edward W. Abel

Researcher at Queen's University Belfast

Publications -  127
Citations -  1218

Edward W. Abel is an academic researcher from Queen's University Belfast. The author has contributed to research in topics: Crystal structure & Denticity. The author has an hindex of 19, co-authored 127 publications receiving 1210 citations. Previous affiliations of Edward W. Abel include University College London & University of Leicester.

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2,2′:6′,2″-Terpyridine (terpy) acting as a fluxional bidentate ligand. Part 4. cis-[M(C6F5)2(terpy)](M = Pd or Pt): nuclear magnetic resonance studies of their solution dynamics and crystal structure of cis-[Pd(C6F5)2(terpy)]

TL;DR: In this article, the rate of terpyridine fluxion was measured by NMR spectroscopy from the exchange effects on the 1H signals of the aromatic hydrogens and in the 19F signals of two C6F5 groups.
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2,2′:6′,2″-Terpyridine (terpy) acting as a fluxional bidentate ligand. Part 1. Trimethylplatinum(IV) halide complexes [PtXMe3(terpy)](X = Cl, Br or I): nuclear magnetic resonance studies of their solution dynamics and crystal structure of [PtIMe3(terpy)]

TL;DR: In this paper, the terpyridine (terpy) reacts with trimethylplatinum halides to form stable octahedral complexes fac-[PtXMe3(terpy)](X = Cl, Br or I) in which the terpy molecule is acting as a bidentate chelate ligand.
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[3]Ferrocenophane bridge reversal barriers

TL;DR: In this paper, the authors used dynamic NMR data for the bridge reversal fluxion of ferrocenophanes with Group VI bridging atoms and made estimates of the relative magnitudes of torsional barriers about single bonds involving like and unlike Group VI atoms.
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The first examples of 2,2′:6′,2″-terpyridine as a fluxional bidentate ligand

TL;DR: In this article, the ligand oscillates between equivalent bidentate forms by a mechanism involving a "tick-tock" twist of the metal moiety through an angle equal to the N-M-N angle of the octahedral centre and involving a seven-coordinate metal intermediate.