CrystEngComm Blog

I recently attended the 30th annual Spring meeting of the British Crystallographic Association at the University of Warwick from 16th-19th April 2012. The program was chaired by Kirsten Christensen (University of Oxford), and included a broad range of lectures from all areas of crystallography.

The Young Crystallographers Group satellite opened the meeting. This is an excellent forum for early stage researchers to present their work in a relaxed and friendly environment. There were 14 students talks in total, all of a very high standard, and two plenaries by Kenneth Shankland and Robin Owen. The Parkin Lecture was awarded to Lynne Thomas (University of Bath) for her outstanding work in outreach and crystallography. Jessica Bland from the Royal Society also came and spoke about the challenges and rewards of science communication, and encouraged everyone to get involved!

Back row: Robin Owen, Claire Murray, Andrew Maloney, Ed Pyzer-Knapp, Karun Arachige. Middle row: Jessica Bland, Alexander Graham, Marco Llamas, Soshichiro Nagano, Thembaninkosi Gaulle, Alan Martin. Front row: Richard Martin, Ioana Sovago, Lynne Thomas, Callum Young, Karim Sutton. With thanks to Allan Pang for the photograph.

The main meeting opened on the second day with a biological group plenary by Laurence Pearl (University of Sussex) discussing his work on the structural biology of the DNA damage response. The subsequent sessions covered multidimensional materials and multidimensional approaches. A forum for opening dialogue between small molecule and macromolecular crystallographers proved to be very popular, with plenty of questions flying between the two communities. Throughout the day there was an art installation by Fevered Sleep called ‘Stilled’ in Warwick arts centre, which used pinhole cameras to capture images of dancers. This was originally commisioned by the Wellcome Trust in 2008, and was very well received at the conference. The evening poster session was very busy, and there was lots of exciting crystallography to be seen and discussed.

The third day of the conference started with a chemical plenary by Robin Taylor in honour of Frank Allen (CCDC), probing the redundancy of crystal structure data. Whilst larger, more complicated structures require a lot more work, the advances in computational chemistry mean it is possible to predict many low energy conformers for smaller organic materials. The morning sessions included awards for early stage scientists. Gareth Lloyd (University of Cambridge) received the CCG/CCDC prize for his work on supramolecular gels. Jon Wright (ESRF) received the physical crystallography prize for his work on the Verwey transition of magnetite. The final award was from the industrial group for the best student talk, and this was awarded to Andrew Maloney (a PhD student in the group of Simon Parsons), who discussed his work on modifying the PIXEL method to calculate intermolecular interaction energies for transition metal complexes. After two sessions on hydrogen bonding, the industrial plenary was given by Dan Shechtman who presented a lively and illuminating overview of his nobel prize winning work on quasi periodic crystals. See my recent interview with Dan here. 

Dan Shechtman pictured. With thanks to Allan Pang for the photograph.

The conference dinner included a ceili and the poster prizes. The CrystEngComm poster prize was awarded to Peter Galek (CCDC) for his poster on ‘H-Bonding landscapes for the assessment of polymorphs, co-crystals & hydrates’. Congratulations Peter!

CrystEngComm poster prize winner Peter Galek

The final day of the conference with the physical plenary by Branton Campbell (Brigham Young University) discussing his work on incommensurate structures using group theory enumeration. Sessions on phases transitions closed the conference. The next BCA Spring meeting will be held in Loughborough in 2014, and will be chaired by Lee Brammer (University of Sheffield).

The last ten years have seen a revolution in our understanding of the mechanisms of biological crystal growth.  Recent studies on crystal nucleation have found evidence of pre-nucleation clusters, a controversial result which apparently contradicts classical nucleation theory.

If you are working in the areas of biomineralisation, biomimetic crystallisation, nucleation or crystal growth then you are very likely to have some significant original research to share. Join a meeting where you can not only discuss your findings but also get them published.

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Crystallisation – A  Biological Perspective: Faraday Discussion 159 is the place to be this July.

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Why choose to come to a Faraday Discussion? They have a unique format – all papers are circulated in advance and all discussion contributions are recorded for publication in the abstract book after the event. You can also have your own poster space at the meeting, so submit yours now before the deadline of 25 May.

A few weeks ago, I attended the 6th annual meeting of the “Control and Prediction of the Organic Solid State” (CPOSS) project in the Old Refectory of University College London. The meeting was themed ‘Crystals or not – where do we go from here?’. There were over 100 delegates in attendance, with both academic and industrial members present.

Sally Price (University College London) opened the morning session with an outline of the CPOSS project achievements to date. Tackling the over-prediction of polymorphs, she issued a caution when deciding that unobserved thermodynamically feasible structures cannot appear. The case of the carbamazepine form V polymorph clearly demonstrated this, as it could in fact be isolated by seeded sublimation! Alastair Florence (University of Strathclyde) followed, focusing on the complementary nature of experimental and computational methods to characterise racemic and enantiopure naproxen. The calculated crystal energy landscape, binary melting point phase diagram, solubility measurements and limited solid-state screening, were all consistent with the racemic Pbca and enantiopure P2₁ compounds being the only practically relevant solid phases of the free acid naproxen.

A slight diversion in theme by Simon Gaisford (University College London) revealed a novel method for identifying polymorphs by thermal methods rather than crystallographic techniques. Different polymorphs have different melting temperatures and heats of fusion. By varying the rate of heating, it was possible to isolate a metastable carbamazepine-nicatinamide cocrystal polymorph. The final talk of the session was by Matthew Hapgood (University College London) who discussed the intriguing case of tetrolic acid, where the lowest global minima of the crystal energy landscape are not the actual alpha or beta polymorphs. By combining solution simulations and nanocrystalline molecular cluster stability calculations, it was possible to extract the actual crystal structures from predictions of energy landscapes.

From left to right: Professor Chick Wilson (University of Bath), Dr Philippe Fernandes (formerly University of Strathclyde), Dr Sharon Cooper (University of Durham), Professor Sally Price (UCL), Professor Jon Steed (University of Durham), Professor Derek Tocher (UCL), Dr Matthew Habgood (UCL), Dr Doris Braun (UCL), Professor Alastair Florence (University of Strathclyde). Photo courtesy of Louise Price.

Following lunch and a busy poster session, the afternoon session started with a presentation by Jon Steed (University of Durham) on crystallisation in anion-switchable supramolecular gels, with a particular focus on producing materials with switchable flow characteristics. Sharon Cooper (University of Durham) offered an interesting way to try to overcome kinetic control of metastable polymorphs (such as the infamous case of Ritonavir) through the use of microemulsions driven by thermodynamic control for polymorphic compounds like mefenamic acid and γ-glycine. Phillippe Fernandes provided a personal overview of his experience in solid-state chemistry, both from an academic and an industrial point of view.

Doris Braun (University College London) emphasized that contact with water cannot be avoided during the manufacturing process of pharmaceuticals. The already complex crystal structure predictions thus require the additional step of hydrate formation predication in order to more accurately predict polymorph formation, such as for 2,4-Dihydroxybenzoic acid and 2,5-Dihydroxybenzoic acid. The session was concluded by Chick Wilson (University of Bath) as a champion of the Directed Assembly of Extended Structures Network. He presented the activities and future plans of this network, which aims to foster collaborations in order to be able to design, engineer and control materials for applications in frontier manufacturing and other industries.

The meeting was enjoyed by all, and was an excellent overview of the current status of structure prediction, as well as highlighting challenges still facing solid-state chemists. Look out for my interview with Sally Price also on the blog!