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      Single-molecule conductance of a chemically modified, {\pi}-extended tetrathiafulvalene and its charge-transfer complex with F4TCNQ

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          Abstract

          We describe the synthesis and single molecule electrical transport properties of a molecular wire containing a \({\pi}\)-extended tetrathiafulvalene (exTTF) group and its charge-transfer complex with F4TCNQ. We form single molecule junctions using the in-situ break junction technique using a home-built scanning tunneling microscope with a range of conductance between 10 G\(_{0}\) down to 10\(^{-7}\) G\(_{0}\). Within this range we do not observe a clear conductance signature of the neutral parent molecule, suggesting either that its conductance is too low or that it does not form stable junctions. Conversely, we do find a clear conductance signature in the experiments carried out on the charge-transfer complex. Due to the fact we expected this species to have a higher conductance than the neutral molecule, we believe this supports the idea that the conductance of the neutral molecule is very low, below our measurement sensitivity. This is further supported by our theoretical calculations. To the best of our knowledge, these are the first reported single molecule conductance measurements on a molecular charge-transfer species.

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          Most cited references36

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          Tetrathiafulvalenes, oligoacenenes, and their buckminsterfullerene derivatives: the brick and mortar of organic electronics.

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            Introduction:  Organic Electronics and Optoelectronics

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              Fullerene for organic electronics.

              This tutorial review surveys and highlights the integration of different molecular wires-in combination with chromophores that exhibit (i) significant absorption cross section throughout the visible part of the solar spectrum and (ii) good electron donating power-into novel electron donor-acceptor conjugates. The focus is predominantly on charge transfer and charge transport features of the most promising systems.
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                Author and article information

                Journal
                25 June 2015
                Article
                10.3762/bjoc.11.120
                1506.07748
                f55dbfe3-e371-442d-9b7f-3ef24613f90f

                http://arxiv.org/licenses/nonexclusive-distrib/1.0/

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                Custom metadata
                Beilstein J.Org.Chem.2015,11,1068-1078
                cond-mat.mes-hall cond-mat.mtrl-sci

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