Website Banner Oxford University Department of Chemistry

Latest News

Congratulations to Patrik Neuhaus for the award of a Feodor Lynen Fellowship from the Alexander von Humboldt Foundation.



Rotaxane

University of Oxford Additional synthetic chemistry expertise is available through Oxford Synthesis Connections

Site Meter

 
Welcome!

Our Group does research in the areas of molecular materials synthesis, supramolecular chemistry, molecular recognition, polymers and dyes. Many of our projects are centred around the synthesis and subsequent physical investigation of porphyrins, rotaxanes and conjugated polymers. All work is directed towards the design and creation of new molecular materials with useful optical, electronic or biomedical properties. We believe that a better understanding of the relationship between molecular structure, molecular function and macroscopic properties will give us the ability to build functional materials on the molecular scale.

Group Images

Recent Publications

A Quaterthiophene-Based Rotaxane: Synthesis, Spectroscopy, and Self-Assembly at Surfaces
L. Zalewski, J. M. Mativetsky, S. Brovelli, M. Bonini, N. Crivillers, T. Breiner, H. L. Anderson, F. Cacialli, P. Samorì
Small 2012 Early View.
Engineering Conjugation in Para-Phenylene-Bridged Porphyrin Tapes
M. Pawlicki, M. Morisue, N. Davis, D. McLean, J. E. Haley, E. Beuerman, M. Drobijev, A. Rebane, A. L. Thompson , S. I. Pascu, G. Accorsi, N. Armaroli, H. L. Anderson
Chem. Sci. 2012, 3, 1541-1547.
Comparison of the Conductance of Three Types of Porphyrin-Based Molecular Wires: β,meso,β-Fused Tapes, meso-Butadiyne-Linked and Twisted meso-meso Linked Oligomers
G. Sedghi, L. J. Esdaile, H. L. Anderson, S. Martin, D. Bethell, S. J. Higgins, R. J. Nichols
Adv. Mater. 2012,, 24, 653-657.
Stepwise Effective Molarities in Porphyrin Oligomer Complexes: Preorganization Results in Exceptionally Strong Chelate Cooperativity
H. J. Hogben, J. K. Sprafke, M. Hoffmann, M. Pawlicki, H. L. Anderson
J. Am. Chem. Soc 2011, 133, 20962-20969.
Belt-Shaped π-Systems: Relating Geometry to Electronic Structure in a Six-Porphyrin Nanoring
J. K. Sprafke, D. V. Kondratuk, M. Wykes, A. L. Thompson, M. Hoffmann, R. Drevinskas, W.-H. Chen, C. K. Yong, J. Kärnbratt, J. E. Bullock, M. Malfois, M. R. Wasielewski, B. Albinsson, L. M. Herz, D. Zigmantas, D. Beljonne, H. L. Anderson
J. Am. Chem. Soc 2011, 133, 17262-17273.
Long-range electron tunnelling in oligo-porphyrin molecular wires
G. Sedghi, V. M. García-Suárez, L. J. Esdaile, H. L. Anderson, C. J. Lambert, S. Martin, D. Bethell, S. J. Higgins, M. Elliott, N. Bennett, J. E. Macdonald, R. J. Nichols
Nat. Nanotech. 2011, 6, 517-523.
Template-directed synthesis of π-conjugated porphyrin [2]rotaxanes and a [4]catenane based on a six-porphyrin nanoring
M. J. Langton, J. D. Matichak, A. L. Thompson, H. L. Anderson
Chem. Sci. 2011, 2, 1897-1901.


Copyright 2005-2012 © Anderson Research Group, University of Oxford, Department of Chemistry, Oxford, UK