Single-Molecule Conductance Behavior of Molecular Bundles.



Bara-Estaún, Alejandro, Planje, Inco J, Almughathawi, Renad, Naghibi, Saman, Vezzoli, Andrea ORCID: 0000-0002-8059-0113, Milan, David C, Lambert, Colin, Martin, Santiago, Cea, Pilar, Nichols, Richard J ORCID: 0000-0002-1446-8275
et al (show 5 more authors) (2023) Single-Molecule Conductance Behavior of Molecular Bundles. Inorganic chemistry, 62 (51). pp. 20940-20947.

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Abstract

Controlling the orientation of complex molecules in molecular junctions is crucial to their development into functional devices. To date, this has been achieved through the use of multipodal compounds (i.e., containing more than two anchoring groups), resulting in the formation of tri/tetrapodal compounds. While such compounds have greatly improved orientation control, this comes at the cost of lower surface coverage. In this study, we examine an alternative approach for generating multimodal compounds by binding multiple independent molecular wires together through metal coordination to form a molecular bundle. This was achieved by coordinating iron(II) and cobalt(II) to 5,5'-bis(methylthio)-2,2'-bipyridine (<b>L</b><sup><b>1</b></sup>) and (methylenebis(4,1-phenylene))bis(1-(5-(methylthio)pyridin-2-yl)methanimine) (<b>L</b><sup><b>2</b></sup>) to give two monometallic complexes, <b>Fe-1</b> and <b>Co-1</b>, and two bimetallic helicates, <b>Fe-2</b> and <b>Co-2</b>. Using XPS, all of the complexes were shown to bind to a gold surface in a <i>fac</i> fashion through three thiomethyl groups. Using single-molecule conductance and DFT calculations, each of the ligands was shown to conduct as an independent wire with no impact from the rest of the complex. These results suggest that this is a useful approach for controlling the geometry of junction formation without altering the conductance behavior of the individual molecular wires.

Item Type: Article
Divisions: Faculty of Science and Engineering > School of Physical Sciences
Depositing User: Symplectic Admin
Date Deposited: 30 Jan 2024 10:13
Last Modified: 30 Jan 2024 10:59
DOI: 10.1021/acs.inorgchem.3c01943
Open Access URL: https://doi.org/10.1021/acs.inorgchem.3c01943
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URI: https://livrepository.liverpool.ac.uk/id/eprint/3178086