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179Michael N. R. Ashfold, Graeme A. King, Daniel Murdock, Michael G. D. NixCurrent address: School of Chemistry, University of Leeds, Leeds, UK LS2 9JT, Thomas A. A. Oliver and Alan G. Sage.
πσ* excited states in molecular photochemistry, Phys. Chem. Chem. Phys., 2010, 12, 1218. Ingo Dauster, Corey A. Rice, Philipp Zielke and Martin A. Suhm.
N–H⋯π interactions in pyrroles: systematic trends from the vibrational spectroscopy of clusters, Phys. Chem. Chem. Phys., 2008, 10, 2827. Olivier Alévêque, Pierre Frère, Philippe Leriche, Tony Breton, Antonio Cravino and Jean Roncali.
Effects of aromatic spacers on the properties of organic field effect transistors based on π-extended tetrathiafulvalene derivatives, J. Mater. Chem., 2009, 19, 3648. Simon Lotz, Chantelle Crause, Andrew J. Olivier, David C. Liles, Helmar Görls, Marilé Landman and Daniela I. Bezuidenhout.
Synthesis and reactivity of metal carbene complexes with heterobiaryl spacer substituents, Dalton Trans., 2009, 697. Alexandra Zamboulis, Nirmalya Moitra, Joël J. E. Moreau, Xavier Cattoën and Michel Wong Chi Man.
Hybrid materials: versatile matrices for supporting homogeneous catalysts, J. Mater. Chem., 2010, 20, 9322. Philip J. Bustard, Guorong Wu, Rune Lausten, Dave Townsend, Ian A. Walmsley, Albert Stolow and Benjamin J. Sussman.
From molecular control to quantum technology with the dynamic Stark effect, Faraday Discuss., 2011, 153, 321. Yujie Ding, Michael A. Invernale, Donna M. D. Mamangun, Amrita Kumar and Gregory A. Sotzing.
A simple, low waste and versatile procedure to make polymer electrochromic devices, J. Mater. Chem., 2011, 21, 11873. Yiyong Huang, Satoru Suzuki, Guokai Liu, Etsuko Tokunaga, Motoo Shiro and Norio Shibata.
Asymmetric synthesis of chiral trifluoromethylated heliotridane via highly catalytic asymmetric Friedel–Crafts alkylation with β-trifluoromethylated acrylates and pyrroles, New J. Chem., 2011, 35, 2614. Stanislav A. Amelichev, Lidia S. Konstantinova, Konstantin A. Lyssenko, Oleg A. Rakitin and Charles W. Rees.
Direct synthesis of fused 1,2,3,4,5-pentathiepins, Org. Biomol. Chem., 2005, 3, 3496.