Unconventional Single-Molecule Conductance Behavior for a New Heterocyclic Anchoring Group: Pyrazolyl
Author(s) -
Lucía Herrer,
Ali K. Ismael,
David C. Milán,
Andrea Vezzoli,
Santiago Martı́n,
Alejandro González Orive,
Iain Grace,
Colin J. Lambert,
José Luís Serrano,
Richard J. Nichols,
Pilar Ce�a
Publication year - 2018
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.8b02051
Subject(s) - anchoring , moiety , conductance , break junction , molecule , protonation , chemistry , electrode , group (periodic table) , crystallography , stereochemistry , materials science , condensed matter physics , organic chemistry , physics , ion , structural engineering , engineering
Electrical conductance across a molecular junction is strongly determined by the anchoring group of the molecule. Here we highlight the unusual behavior of 1,4-bis(1H-pyrazol-4-ylethynyl)benzene that exhibits unconventional junction current versus junction-stretching distance curves, which are peak-shaped and feature two conducting states of 2.3 × 10 -4 G 0 and 3.4 × 10 -4 G 0 . A combination of theory and experiments is used to understand the conductance of single-molecule junctions featuring this new anchoring group, i.e., pyrazolyl. These results demonstrate that the pyrazolyl moiety changes its protonation state and contact binding during junction evolution and that it also binds in either end-on or facial geometries with gold contacts. The pyrazolyl moiety holds general interest as a contacting group, because this linkage leads to a strong double anchoring of the molecule to the gold electrode, resulting in enhanced conductance values.
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