When Dihedral Angles Mask Denticity in Molecular Conductance

Stronger molecule-electrode coupling is associated with higher conductance in single-molecule junctions. This has been taken to imply that more coordination-what will be referred to here as higher denticity-between the molecule and the electrode is expected to impart higher conductance to the overall junction. Herein, this assumption using a single molecule construct, a rigid N-heterohexacene molecule with tetradentate ethyl sulfide (-SEt) anchors, is examined. Thus, rather than comparing a series of molecules with different anchoring groups, it is investigated how variations in effective denticity arise naturally within one molecule. Using the nonequilibrium Green's function technique in conjunction with density functional theory and mechanically controlled break-junction (MCBJ) experiments, it is found that increasing the denticity between the molecule and the electrode does not yield the expected higher conductance. Instead, simulated break-junction traces reveal a strong correlation between conductance and the dihedral angle between the electrode and the molecular core, with changes to dihedral angles providing far more variation in conductance values than denticity alone. In fact, it is shown that counter to naïve expectations, different denticities cannot be distinguished by conductance, merging instead into a single conductance feature. This is supported by MCBJ experiments on this molecule, where only a single conductance state is identified, suggesting that the expected denticity-dependent multistate conductance behavior is dominated by the effect of dihedral angles. By restricting dihedral angles to more favorable values by molecular design, the calculations show that significantly higher conductance values can still be achieved despite the limitations imposed by dihedral-denticity coupling. The work demonstrates that mere denticity may not be sufficient to design highly conductive molecular junctions, and that the association of conductance features with different denticities should be treated with caution.

Authors

Institutions

Publication Details

Journal
ChemPhysChem
Published
2025-11-28
DOI
https://doi.org/10.1002/cphc.202500816
Primary Topic
Molecular Junctions and Nanostructures
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

When Dihedral Angles Mask Denticity in Molecular Conductance

Oliver L. A. Monti, Rashmi Yohani Amarakoon Arachchige, Manuel Smeu, Dylan Dyer et al.
ChemPhysChem
Molecular Junctions and Nanostructures
article

When Dihedral Angles Mask Denticity in Molecular Conductance

Oliver L. A. Monti, Rashmi Yohani Amarakoon Arachchige, Manuel Smeu, Dylan Dyer, Tarek H. El‐Assaad, Dominic V. McGrath, M. Peiris, Kevin Batzinger, Sophie Lamotte
article en

Abstract

Stronger molecule-electrode coupling is associated with higher conductance in single-molecule junctions. This has been taken to imply that more coordination-what will be referred to here as higher denticity-between the molecule and the electrode is expected to impart higher conductance to the overall junction. Herein, this assumption using a single molecule construct, a rigid N-heterohexacene molecule with tetradentate ethyl sulfide (-SEt) anchors, is examined. Thus, rather than comparing a series of molecules with different anchoring groups, it is investigated how variations in effective denticity arise naturally within one molecule. Using the nonequilibrium Green's function technique in conjunction with density functional theory and mechanically controlled break-junction (MCBJ) experiments, it is found that increasing the denticity between the molecule and the electrode does not yield the expected higher conductance. Instead, simulated break-junction traces reveal a strong correlation between conductance and the dihedral angle between the electrode and the molecular core, with changes to dihedral angles providing far more variation in conductance values than denticity alone. In fact, it is shown that counter to naïve expectations, different denticities cannot be distinguished by conductance, merging instead into a single conductance feature. This is supported by MCBJ experiments on this molecule, where only a single conductance state is identified, suggesting that the expected denticity-dependent multistate conductance behavior is dominated by the effect of dihedral angles. By restricting dihedral angles to more favorable values by molecular design, the calculations show that significantly higher conductance values can still be achieved despite the limitations imposed by dihedral-denticity coupling. The work demonstrates that mere denticity may not be sufficient to design highly conductive molecular junctions, and that the association of conductance features with different denticities should be treated with caution.

ChemPhysChemVol. 27(4)
Binghamton University (US), University of Arizona (US)
National Science Foundation, Alfred P. Sloan Foundation, University of Arizona, Division of Materials Research, Division of Electrical, Communications and Cyber Systems
Openalex Percentile: Top 63%
Molecular Junctions and Nanostructures
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.