Senior Research Associate (X-Ray Crystallography)
Chemical Crystallography
Crystallographic methods provide detailed atomic-level descriptions of crystalline solids, including molecular structure and geometrical information on intermolecular interactions.
Single-crystal and powder X-ray diffraction are core analytical techniques within the chemical sciences, which support and augment a broad range of research within the Department. Modern diffraction instruments, applied at both laboratory and synchrotron sources, enable complex chemical problems to be tackled using crystallographic methods: for example, characterizing and understanding the consequences of disorder in molecular crystals or monitoring chemical changes in single crystals or crystalline powders.
Publications
A general synthetic methodology to access magnesium aluminate electrolyte systems for Mg batteries
– Journal of Materials Chemistry A
(2019)
7,
2677
(doi: 10.1039/c8ta10295c)
On the kinetics of solvate formation through mechanochemistry
– Crystengcomm
(2019)
21,
2097
(doi: 10.1039/c8ce00871j)
Deprotonation, insertion and isomerisation in the post-functionalisation of tris-pyridyl aluminates
– Dalton Transactions
(2019)
48,
5692
(doi: 10.1039/c9dt00869a)
Use of a fluorinated probe to quantitatively monitor amino acid binding preferences of ruthenium(ii) arene complexes.
– Dalton Transactions
(2019)
48,
6910
(doi: 10.1039/c8dt05159c)
Synthesis of 1,2-Diphospholides Using a Main Group “Superbase”
– Organometallics
(2018)
37,
4465
Post-functionalisation of Tris-pyridyl Aluminate Ligands; Chirality, Coordination and Supramolecular Chemistry
– Chemistry (Weinheim an der Bergstrasse, Germany)
(2018)
24,
17019
(doi: 10.1002/chem.201803342)
Postfunctionalization of Tris(pyridyl) Aluminate Ligands: Chirality, Coordination, and Supramolecular Chemistry
– Chemistry – A European Journal
(2018)
24,
16929
(doi: 10.1002/chem.201804887)
Front Cover: Postfunctionalization of Tris(pyridyl) Aluminate Ligands: Chirality, Coordination, and Supramolecular Chemistry (Chem. Eur. J. 64/2018)
– Chemistry - A European Journal
(2018)
24,
16925
(doi: 10.1002/chem.201804886)
Semi-syntheses of the 11-hydroxyrotenoids sumatrol and villosinol.
– Organic & Biomolecular Chemistry
(2018)
16,
6395
(doi: 10.1039/c8ob01919c)
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