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Nicola L. Bell

Researcher at University of Glasgow

Publications -  33
Citations -  661

Nicola L. Bell is an academic researcher from University of Glasgow. The author has contributed to research in topics: Chemistry & Computer science. The author has an hindex of 11, co-authored 27 publications receiving 405 citations. Previous affiliations of Nicola L. Bell include University of Edinburgh & University of St Andrews.

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Influence of Intracerebral Hemorrhage Location on Incidence, Characteristics, and Outcome Population-Based Study

Neshika Samarasekera, +162 more
- 01 Feb 2015 - 
TL;DR: The baseline characteristics and outcome of lobar ICH differ from other locations, and this population-based, prospective inception cohort study of ICH identified and validated ICH diagnoses in 2010 to 2011 in an adult population of 695 335.
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Thorium Mono- and Bis(imido) Complexes Made by Reprotonation of cyclo-Metalated Amides

TL;DR: X-ray and computational structural analyses show a "transition-metal-like" cis-bis(imido) geometry and polarized Th═N bonds with twice the Wiberg bond order of the formally single Th-N bond in the same molecule.
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Inner-sphere vs. outer-sphere reduction of uranyl supported by a redox-active, donor-expanded dipyrrin

TL;DR: In this article, the uranyl(vi) complex UO2Cl(L) of the redox-active, acyclic diimino-dipyrrin anion, L- is reported and its reaction with inner and outer-sphere reductants studied Voltammetric, EPR-spectroscopic and X-ray crystallographic studies.
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An Autonomous Chemical Robot Discovers the Rules of Inorganic Coordination Chemistry without Prior Knowledge.

TL;DR: A chemical discovery robot designed to search for areas of reactivity found through autonomous selection of the reagent types, amounts, and reaction conditions aiming for combinations that are reactive is presented.
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Uranyl to Uranium(IV) Conversion through Manipulation of Axial and Equatorial Ligands

TL;DR: The controlled manipulation of the axial oxo and equatorial halide ligands in the uranyl dipyrrin complex, UO2Cl(L), allows the Uranyl reduction potential to be shifted by 1.53 V into the range accessible to naturally occurring reductants that are present during uranium remediation and storage processes.