[28-11-2016]

Understanding the transport of charge across non-covalently bonded  molecules is key to our understanding of many diverse systems, from  oxidative damage and repair of DNA to the efficiency of organic  electronic materials. Single-molecule break junctions are an important  stage on which to test and develop this understanding and they have now  been used by Delft researchers Ferdinand C. Grozema, Herre S. J. van der Zant and  colleagues to show that electronic transport through a π-stacked  dimer can be precisely controlled by mechanically manipulating its  conformation and thus turning destructive interference effects ON or  OFF. The cover shows the electrodes of a break junction connected by a π-stacked dimer, the molecular orbitals of which are also shown. 
Abstract
Recent observations of destructive quantum interference in  single-molecule junctions confirm the role of quantum effects in the  electronic conductance properties of molecular systems. These effects  are central to a broad range of chemical and biological processes and  may be beneficial for the design of single-molecule electronic  components to exploit the intrinsic quantum effects that occur at the  molecular scale. Here we show that destructive interference can be  turned on or off within the same molecular system by mechanically  controlling its conformation. Using a combination of ab initio  calculations and single-molecule conductance measurements, we  demonstrate the existence of a quasiperiodic destructive  quantum-interference pattern along the breaking traces of π-stacked  molecular dimers. The results demonstrate that it is possible to  control the molecular conductance over more than one order of magnitude  and with a sub-ångström resolution by exploiting the subtle  structure–property relationship of π-stacked dimers.
Full article: Riccardo Frisenda, Vera A. E. C. Janssen, Ferdinand C. Grozema, Herre S. J. van der Zant & Nicolas Renaud (2016): 'Mechanically controlled quantum interference in individual π-stacked dimers'. Nature Chemistry 8,1099–1104 doi:10.1038/nchem.2588