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Yusuf Hamied Department of Chemistry

 

Materials Chemistry Group


Functional (pharmaceutical) molecular solids


The design of functional molecular materials has advanced tremendously through cocrystallisation: the assembly of multiple chemical species in the same crystal lattice. Underlying cocrystals formation are rules that guide molecular recognition and self-assembly. We are deciphering this "intermolecular language" by combining experimental work with data mining and molecular modelling. Our particular interest is constructing functional materials through weak supramolecular interactions, such as hydrogen and halogen bonds.



Surface dynamics of molecular solids


Properties of crystalline solids are usually measured as a bulk property, and the results interpreted in terms of crystal structure. However, such a description does not adequately describe the surface of molecular crystals, at which the distribution of forces on a molecule is non-symmetrical, resulting in high mobility and reactivity. The atomic force microscope (AFM) is a unique tool for studying such surface-related dynamics.


 


Teaching


 


Current teaching includes a third year undergraduate lecture course on the Chemistry of Materials.  The course examines a range of organic, metal-organic and inorganic materials and demonstrates their varied uses. We will, in particular, identify important structural features relevant to such areas as the pharmaceutical and petrochemical industries and to naturally occurring biomaterials such as bone. The underlying chemistry and properties will be shown to be often sensitive to the way that the constituent atoms and molecules are packed together. This aspect of solid state control will be examined in some detail.



The development and design of new materials, incorporating structural characteristics of inorganic solids and functionality of organic molecules will be described.



The control of crystal morphology is important in many applications, and this will be discussed in the context of templating crystal growth, both in Nature and in the laboratory, and of crystal engineering. Numerous important materials, including many found in Nature, are in fact inorganic-organic composites, and these will also be discussed in detail.



From paracetamol to petrol to proteins to bone – the importance of the Chemistry of Materials will be explored in these lectures.


Also, as part of the Cambridge fourth year program I teach a course on Organic Solids that builds on the lecture course Chemistry of Materials given in Part II (although it is not required that students have taken this course). The first six lectures of the course, given by me, will cover aspects of crystal chemistry, structure and reactivity of organic solids. Examples of lattice controlled reactions will be given, including photochemical and thermal. Particular emphasis will be placed on how solid state properties impact on the development of drug products in the pharmaceutical industry. Experimental approaches to understanding molecular packing will be described and will lead into the second part of the course, given by my colleague, Dr Graeme Day.

Publications

A Czerny‐Turner spectrograph incorporating a 2‐stage image intensifier for the study of very weak Raman spectra
DV Willetts, PA Freedman, WJ Jones
– Journal of Raman Spectroscopy
(2005)
2,
249
4-Methyl-3,5-dinitrobenzoic acid-dimethyl sulfoxide (1/1)
AV Trask, M Abthorpe, W Jones
– Acta Crystallographica Section E: Structure Reports Online
(2005)
61,
o1100
Crystal Engineering of Organic Cocrystals by the Solid-State Grinding Approach
AV Trask, W Jones
– Topics in Current Chemistry
(2005)
254,
41
3,5-Dinitrobenzoic acid–dimethyl sulfoxide (1/1)
M Abthorpe, AV Trask, W Jones
– Acta Crystallographica Section E: Crystallographic Communications
(2005)
61,
O609
Pharmaceutical cocrystallization: Engineering a remedy for caffeine hydration
AV Trask, WDS Motherwell, W Jones
– Crystal Growth & Design
(2005)
5,
1013
Beyond the Isotropic Atom Model in Crystal Structure Prediction of Rigid Molecules:  Atomic Multipoles versus Point Charges
GM Day, WDS Motherwell, W Jones
– Crystal Growth & Design
(2005)
5,
1023
Selective polymorph transformation via solvent -drop grinding
AV Trask, N Shan, WDS Motherwell, W Jones, S Feng, RBH Tan, KJ Carpenter
– Chemical Communications
(2005)
880
Hydrogen bonding preference of equatorial versus axial hydroxyl groups in pyran and cyclohexane rings in organic crystals
A Bonnet, J Chisholm, WDS Motherwell, W Jones
– CrystEngComm
(2005)
7,
71
Occurrence of Pharmaceutically Acceptable Anions and Cations in the Cambridge Structural Database
DA Haynes, W Jones, WD Samuel Motherwell
– Journal of Pharmaceutical Sciences
(2005)
94,
2111
A molecular dynamics simulation of the melting points and glass transition temperatures of myo- and neo-inositol.
SW Watt, JA Chisholm, W Jones, S Motherwell
– J Chem Phys
(2004)
121,
9565
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Research Group

Research Interest Groups

Telephone number

01223 336468

Email address

wj10@cam.ac.uk