The first excited state of conjugated donor-acceptor molecules of C3 symmetry (octupolar molecules) is doubly degenerate. Such a doublet is known to be isomorphic to a spin 1/2. It is shown that a large electric dipole moment is associated with this spin. Since the mean value of the electric dipole moment of an octupolar molecule is a measure of the symmetry breaking charge transfer, a dimensionless dipole moment called the dissymmetry vector is introduced. The dissymmetry vector operator is constructed. A linear tensor connection between this operator and the Pauli matrices is found. The tensor character is due to the two-dimensionality of the dipole moment. The dipole moment can rotate freely in the plane of the molecule as long as the C3 symmetry is maintained. The rotation is associated only with the rearrangement of the electronic subsystem of the molecule and does not affect the spatial position of the nuclei. This opens up the possibility of changing the dipole moment state on a subpicosecond time scale. The Jahn-Teller effect on the dissymmetry vector is considered in detail. It is shown that the dissymmetry vector can be controlled using electric fields in the same way as three-dimensional spin if both static and alternating electric fields are in the plane of the molecule. The conducted studies indicate that the dipole moment of excited octupolar molecules is a promising candidate for the physical implementation of a qubit.
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http://dx.doi.org/10.1063/5.0243375 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Guangzhou University, Center for Advanced Analytical Science, c/o School of Chemistry and Chemical Engineering, 230 Wai Huan Xi Road, Guangzhou Higher Education Mega Center, Guangzhou 510006 P, 510006, Guangzhou, CHINA.
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January 2025
Department of Chemistry, Graduate School of Science, Kyoto University, Kitashirakawa-Oiwakecho, Sakyo-ku, Kyoto 606-8502, Japan.
We investigated the gas-liquid interface of aqueous solutions containing phenol and related aromatic compounds using extreme ultraviolet laser photoelectron spectroscopy and molecular dynamics simulations. The interfacial densities of protonated and deprotonated forms of phenol, aniline, and 4-nitrophenol were found to be primarily determined by their surface affinities and exhibit similar concentration dependences to their respective bulk densities. Despite the distinct interfacial orientations of their permanent dipole moments, these compounds monotonically decreased the surface potential at higher concentrations.
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Department of Chemistry, Aarhus University, Langelandsgade 140, DK-8000 Aarhus, Denmark.
The minimal basis iterative Stockholder (MBIS) decomposition of molecular electron densities into atomic quantities is an attractive approach for deriving electrostatic parameters in force fields. The MBIS-derived atomic charges, however, in general tend to overestimate the molecular dipole and quadrupole moments by ∼10%. We show that it is possible to derive a constrained MBIS model where the atomic charges or a combination of atomic charges and dipoles exactly reproduce the molecular dipole and quadrupole moments for molecules.
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Microsoft Research AI for Science, 21 Station Road, Cambridge CB1 2FB, United Kingdom.
Variational ab initio methods in quantum chemistry stand out among other methods in providing direct access to the wave function. This allows, in principle, straightforward extraction of any other observable of interest, besides the energy, but, in practice, this extraction is often technically difficult and computationally impractical. Here, we consider the electron density as a central observable in quantum chemistry and introduce a novel method to obtain accurate densities from real-space many-electron wave functions by representing the density with a neural network that captures known asymptotic properties and is trained from the wave function by score matching and noise-contrastive estimation.
View Article and Find Full Text PDFOrg Lett
January 2025
School of Pharmacy, Yantai University, Yantai 264005, P. R. China.
Compared with the energetically favorable 5- or 6-membered fluoro-functionalized heterocycles, the construction of medium-sized fluoro-heterocycles is relatively under-researched because of their inherently unfavorable enthalpic and entropic nature. Based on rational design and DFT calculations, a novel photocatalytic difluoromethyl radical-initiated intramolecular 7--trig cyclization was realized, thus affording a sustainable route for the synthesis of challenging fluoro-functionalized medium-sized -heterocycles. Depending on atomic dipole moment corrected Hirshfeld population (ADCH) charge calculations, the chemoselective 6--trig radical cyclizations were further replenished.
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