Matthew Rosseinsky

Professor of Inorganic Chemistry at the University of Liverpool.

Biography

​Matthew Rosseinsky obtained a degree and a D. Phil in Chemistry from the University of Oxford in 1990. He was a Postdoctoral Member of Technical Staff at A.T.&T. Bell Laboratories then in 1992 was appointed University Lecturer in Chemistry at the University of Oxford. In 1999 he moved to the University of Liverpool as Professor of Inorganic Chemistry. He was elected a Fellow of the Royal Society in 2008, and was awarded the Hughes Medal of the Royal Society in 2011. In 2013 he became a Royal Society Research Professor. He was awarded the inaugural de Gennes Prize for Materials Chemistry (a lifetime achievement award open internationally) by the Royal Society of Chemistry in 2009, the C.N.R. Rao Award of the Chemical Research Society of India in 2010 and gave the Muetterties Lectures at UC Berkeley and Lee Lectures at the University of Chicago in 2017. He was awarded the Davy Medal of the Royal Society in 2017. He was a member of the governing Council of the Engineering and Physical Sciences Research Council from 2015 - 2019. His work addresses the synthesis of new functional materials in bulk and thin film form for energy and information storage applications, and has been characterised by extensive collaboration with many academic and industrial colleagues. Current areas of interest include materials for batteries and solid oxide fuel cells, multiferroics, thermoelectrics, superconductivity, materials for separations and catalysis, high-throughput materials discovery, and materials for solar energy conversion. His group is developing an integrated computational and experimental approach to materials discovery, including new tools for crystal structure prediction.

All sessions by Matthew Rosseinsky

Porous materials and rotation about single bonds
02:00 AM

One of the distinguishing features of metal-organic frameworks and other non-traditional porous materials, such as interlocked cage molecules, is their ability to respond flexibly to changes in their environment by changing their structures. There are a variety of mechanisms for this, including the relative displacement of two rigid networks and the repositioning of a linker with respect to an inorganic building unit. We have concentrated on rotations about single bonds in organic linkers as a route to change structures that has some similarities with the restructuring mechanisms adopted by biological molecules. This presentation will both review progress and cover recent results that include a new system that adopts multiple distinct crystal structures by this single bond rotation mechanism.(1)

Matthew Rosseinsky

Professor of Inorganic Chemistry at the University of Liverpool.

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