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Understanding and controlling quantum interference (QI) in single molecules is fundamental to the development of QI-based single-molecule electronics. Simple rules such as counting rules, curly arrow rules (CARs), circuit rules, and more recently magic ratio rules have been developed to predict QI patterns in polycyclic aromatic hydrocarbons. CARs are widely used to predict destructive QI. Here we examine the validity of CARs in fully conjugated anthracene and dihydroxyanthracene, cross-conjugated anthraquinone, and broken conjugated dihydroanthracene attached to either graphene or gold electrodes through π-π stacking or thiol and Au-C anchors. For the first time, we demonstrate that CARs break down in molecular junctions formed by cross-conjugated anthraquinone. In contrast with the destructive QI predicted by CARs for a meta-connected anthraquinone core, we demonstrate that QI is constructive. This behavior is independent of the choice of electrode material or anchor groups. This is significant, because by changing the redox state of meta-connected dihydroxyanthracene to form meta-connected anthraquinone, the conductance of the junction increases by a couple of orders of magnitude due to the crossover from constructive to destructive QI. This opens new avenues for realization of QI-based single-molecule switches.
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http://dx.doi.org/10.1002/anie.201807257 | DOI Listing |
J Comput Chem
July 2025
Laboratory of Theoretical Chemistry (LCT) Namur Institute of Structured Matter (NISM), University of Namur, Namur, Belgium.
Using the framework of the bonding evolution theory (BET), we investigated the molecular mechanism of the [3+2] cycloaddition reaction of benzonitrile oxide (1) with five ethylenic derivatives (2a-e). The global mechanism consists in the concerted attack of one of the O lone pairs of 1 on one of the atoms of the C-X double or triple bond of 2 (X = C, O, N), the attack of the C-X double or triple bond of 2 on the C of the C-N triple bond of 1, and the conversion of C-N triple bond of 1 into a double bond and the creation of a lone pair on N. The reaction proceeds through a one-step mechanism, the creation and modification of the electron basins occur at different places along the intrinsic reaction coordinate, as unraveled by the BET study.
View Article and Find Full Text PDFChem Sci
October 2024
Department of Chemistry and Research Institute of Basic Sciences, Incheon National University Republic of Korea
An array of thiophene-based π-conjugated linkers in covalently linked pentacene dimers allow us to access diverse quantum interference (QI), modulating nonadiabatic coupling (NAC) in the singlet fission (SF) process. Simulations show that structural isomerism in terms of S atom orientation substantially alters NAC with relatively marginal impacts on energies. Extended curly arrow rules (ECARs) reveal sensitive dependence of QI on SF linker topologies and connectivity, categorizing regimes of constructive, destructive, and previously unrealized in SF research, shifted destructive QI.
View Article and Find Full Text PDFJ Phys Chem A
February 2022
ARC Centre of Excellence in Exciton Science, School of Chemistry, UNSW, Sydney, New South Wales 2052, Australia.
The electronic wave function of molecules is 3-dimensional and inseparable in the coordinates of the electrons. Whereas molecular orbitals are often invoked to visualize the electronic structure, they are nonunique, with the same 3-dimensional wave function being represented by an infinite number of 3-D, one-electron functions (orbitals). Furthermore, multireference wave functions cannot be described by an antisymmetrized product of a single set of occupied orbitals.
View Article and Find Full Text PDFJ Phys Chem C Nanomater Interfaces
August 2021
Department of Chemistry, Durham University, Lower Mountjoy, Stockton Road, Durham DH1 3LE, U.K.
Controlling charge transport through molecular wires by utilizing quantum interference (QI) is a growing topic in single-molecular electronics. In this article, scanning tunneling microscopy-break junction techniques and density functional theory calculations are employed to investigate the single-molecule conductance properties of four molecules that have been specifically designed to test extended curly arrow rules (ECARs) for predicting QI in molecular junctions. Specifically, for two new isomeric 1-phenylpyrrole derivatives, the conductance pathway between the gold electrodes must pass through a nitrogen atom: this novel feature is designed to maximize the influence of the heteroatom on conductance properties and has not been the subject of prior investigations of QI.
View Article and Find Full Text PDFNanoscale
January 2021
Department of Chemistry, Durham University, Lower Mountjoy, Stockton Road, Durham, DH1 3LE, UK.
The ability to easily and reliably predict quantum interference (QI) behaviour would facilitate the design of functional molecular wires with potential applications in switches, transistors and thermoelectric devices. A variety of predictive methods exist, but with the exception of computationally-expensive DFT-based charge transport simulations, these often fail to account for the experimentally observed behaviour of molecules that differ significantly in structure from alternant polycyclic aromatic hydrocarbons. By considering a range of prior studies we have developed an extension to predictive "curly arrow rules".
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