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CMP
Credit: Jack Hobhouse

David Keen

Visiting Professor

Sub department

  • Condensed Matter Physics

Research groups

  • X-ray and neutron scattering
david.keen@physics.ox.ac.uk
Telephone: 01865 (2)72310
Clarendon Laboratory, room 106
  • About
  • Publications

Ball-milling-induced amorphization of zeolitic imidazolate frameworks (ZIFs) for the irreversible trapping of iodine.

Chemistry (Weinheim an der Bergstrasse, Germany) 19:22 (2013) 7049-7055

Authors:

Thomas D Bennett, Paul J Saines, David A Keen, Jin-Chong Tan, Anthony K Cheetham

Abstract:

The I2-sorption and -retention properties of several existing zeolitic imidazolate frameworks (ZIF-4, -8, -69) and a novel framework, ZIF-mnIm ([Zn(mnIm)2 ]; mnIm=4-methyl-5-nitroimidazolate), have been characterised using microanalysis, thermogravimetric analysis and X-ray diffraction. The topologically identical ZIF-8 ([Zn(mIm)2]; mIm=2-methylimidazolate) and ZIF-mnIm display similar sorption abilities, though strikingly different guest-retention behaviour upon heating. We discover that this guest retention is greatly enhanced upon facile amorphisation by ball milling, particularly in the case of ZIF-mnIm, for which I2 loss is retarded by as much as 200 °C. It is anticipated that this general approach should be applicable to the wide range of available metal-organic framework-type materials for the permanent storage of harmful guest species.
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Aminoff Prize in crystallography

Physica Scripta IOP Publishing 87:4 (2013) 048101
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Bifurcated Polarization Rotation in Bismuth‐Based Piezoelectrics

Advanced Functional Materials Wiley 23:2 (2013) 185-190

Authors:

Dean S Keeble, Emma R Barney, David A Keen, Matthew G Tucker, Jens Kreisel, Pam A Thomas
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Dynamic disorder and the α-β phase transition in quartz-type FePO4 at high temperature investigated by total neutron scattering, Raman spectroscopy, and density functional theory

Physical Review B American Physical Society (APS) 86:13 (2012) 134104

Authors:

GM Bhalerao, P Hermet, J Haines, O Cambon, DA Keen, MG Tucker, E Buixaderas, P Simon
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Inhibition of D-xylose isomerase by polyols: atomic details by joint X-ray/neutron crystallography.

Acta crystallographica. Section D, Biological crystallography 68:Pt 9 (2012) 1201-1206

Authors:

Andrey Kovalevsky, B Leif Hanson, Sax A Mason, V Trevor Forsyth, Zoe Fisher, Marat Mustyakimov, Matthew P Blakeley, David A Keen, Paul Langan

Abstract:

D-Xylose isomerase (XI) converts the aldo-sugars xylose and glucose to their keto analogs xylulose and fructose, but is strongly inhibited by the polyols xylitol and sorbitol, especially at acidic pH. In order to understand the atomic details of polyol binding to the XI active site, a 2.0 Å resolution room-temperature joint X-ray/neutron structure of XI in complex with Ni(2+) cofactors and sorbitol inhibitor at pH 5.9 and a room-temperature X-ray structure of XI containing Mg(2+) ions and xylitol at the physiological pH of 7.7 were obtained. The protonation of oxygen O5 of the inhibitor, which was found to be deprotonated and negatively charged in previous structures of XI complexed with linear glucose and xylulose, was directly observed. The Ni(2+) ions occupying the catalytic metal site (M2) were found at two locations, while Mg(2+) in M2 is very mobile and has a high B factor. Under acidic conditions sorbitol gains a water-mediated interaction that connects its O1 hydroxyl to Asp257. This contact is not found in structures at basic pH. The new interaction that is formed may improve the binding of the inhibitor, providing an explanation for the increased affinity of the polyols for XI at low pH.
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