Tracking molecular resonance forms of donor-acceptor push-pull molecules by single-molecule conductance experiments

被引:38
|
作者
Lissau, Henriette [1 ]
Frisenda, Riccardo [2 ]
Olsen, Stine T. [1 ]
Jevric, Martyn [1 ]
Parker, Christian R. [1 ]
Kadziola, Anders [1 ]
Hansen, Thorsten [1 ]
van der Zant, Herre S. J. [2 ]
Nielsen, Mogens Brondsted [1 ]
Mikkelsen, Kurt V. [1 ]
机构
[1] Univ Copenhagen, Dept Chem, DK-2100 Copenhagen, Denmark
[2] Delft Univ Technol, Kavli Inst Nanosci, NL-2600 GA Delft, Netherlands
关键词
QUANTUM INTERFERENCE; TRANSPORT; ELECTRONICS; SIGNATURES; CONTINUUM; ANALOGS;
D O I
10.1038/ncomms10233
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ability of molecules to change colour on account of changes in solvent polarity is known as solvatochromism and used spectroscopically to characterize charge-transfer transitions in donor-acceptor molecules. Here we report that donor-acceptor-substituted molecular wires also exhibit distinct properties in single-molecule electronics under the influence of a bias voltage, but in absence of solvent. Two oligo(phenyleneethynylene) wires with donor-acceptor substitution on the central ring (cruciform-like) exhibit remarkably broad conductance peaks measured by the mechanically controlled break-junction technique with gold contacts, in contrast to the sharp peak of simpler molecules. From a theoretical analysis, we explain this by different degrees of charge delocalization and hence cross-conjugation at the central ring. Thus, small variations in the local environment promote the quinoid resonance form (off), the linearly conjugated (on) or any form in between. This shows how the conductance of donor-acceptor cruciforms is tuned by small changes in the environment.
引用
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页数:8
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