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Dmitry A. Cheshkov

Publications and source records attributed to Dmitry A. Cheshkov.

5 recordsLinked to original sources

Symmetry of Spin Systems as Automorphisms of Undirected Weighted Graphs: Realizability Criterion and Complete Taxonomy up to 14 Spins

Exact simulation of high-resolution NMR spectra requires block diagonalization of the spin Hamiltonian, whose dimension grows exponentially with the number of spins $N$; symmetry is the principal tool for taming this growth, yet which permutation groups can occur as the full symmetry group of a scalar-coupled spin system has lacked an exhaustive treatment. Formulating the spin system as an undirected edge-weighted complete graph, we prove an exact realizability criterion: a subgroup of $S_N$ is realizable if and only if it coincides with its symmetrized (undirected) Wielandt 2-closure. In particular, purely rotational symmetry of a single spin ring is impossible, yet chiral spin systems do exist as multi-orbit twisted stacks, and we determine the minimal spin count $μ^{*}(C_n)$ for every cyclic group, including the counter-intuitive realizations $C_8$ and $C_9$ at $N = 12$. A sequential symmetrization algorithm, completed by an orbit-partition decomposition, yields a provably exhaustive enumeration of all realizable symmetry types up to $N = 14$: the apparently new sequence $a(N) = 1, 1, 3, 8, 11, 27, 36, 90, 131, 282, 394, 948, 1316, 2866$ with the tower law $a(N) = a(N-1) + f(N)$ - a catalogue of 6112 entries in all, organized by canonical identifiers and a structural grammar extending the Pople nomenclature. Finally, we present a hierarchical methodology for exact block diagonalization without physical approximations: factorization by the conserved total spin projection, Schur-Weyl contraction of magnetically equivalent composites, orbit-weight deduplication of the spin configurations, and isotypic projection over the representations of the factor group, with a uniform treatment of non-abelian groups and complex characters.

physics.chem-ph↗

On the Connection of High-Resolution NMR Spectrum Mirror Symmetry With Spin System Properties

A correlation between the symmetry of NMR spectra, including higher-order spectra, and the properties of the spin system has been established. It is shown that for a spectrum to be symmetric about the mid-resonance frequency (ν0), two conditions must be satisfied: the resonant frequencies of the spins must be symmetrically positioned about ν0, and the J coupling matrix must be symmetric about the secondary diagonal. The results were validated by calculating theoretical spectra for 4-, 5-, and 6-spin systems.

physics.chem-ph↗

Mirror Symmetry of the NMR Spectrum and the Connection with the Structure of Spin Hamiltonian Matrix Representations

This work provides a comprehensive theoretical framework for understanding the symmetry properties of High-Resolution NMR spectra. We analyze the conditions under which a spectrum exhibits mirror symmetry (palindromicity). We demonstrate that such symmetry can arise from two distinct mechanisms: (1) the direct geometric bisymmetry of the Hamiltonian matrix in a generalized canonical basis (typical for balanced systems like $A_nB_n$ or $A_nX_n$), and (2) a more fundamental property of topological isospectrality (similarity) under parameter exchange induced by the internal symmetry of the spin system, which applies even when the matrix lacks geometric symmetry (as observed in $AA'BB'$ systems).

physics.chem-ph↗

Total lineshape analysis of α-tetrahydrofuroic acid $^{1}$H NMR spectra

The 1H NMR spectra of L-proline oxygen analogous, alpha-tetrahydrofuroic acid, 7-spins nonsymmetric spin system with strongly pronounced non-first order effects were analyzed by ANATOLIA total lineshape fitting. A close agreement of theoretical and experimental spectra (with R-Factor values bellow 5%) was achieved and accurate values of coupling constant were obtained. The carboxylic substituent disrupts tetrahydrofuran symmetry and allows to unambiguously determine the typical values of geminal coupling constants in oxygen-containing saturated five-membered ring systems.

physics.chem-ph↗

Photochemically induced dynamic nuclear polarization of heteronuclear singlet order

Photochemically induced dynamic nuclear polarization (photo-CIDNP) is a method to hyperpolarize nuclear spins using light. In most cases, CIDNP experiments are performed at a high magnetic field and the sample is irradiated by the light inside a nuclear magnetic resonance (NMR) spectrometer. Here we demonstrate photo-CIDNP hyperpolarization generated in the Earth magnetic field and under zero- to ultralow field (ZULF) conditions. Irradiating a sample for several seconds with inexpensive light-emitting diodes produces a strong hyperpolarization of 1H and 13C nuclear spins enhancing the NMR signals several hundred times. The hyperpolarized spin states at the Earth field and in ZULF are different. In the latter case, the state corresponds to the singlet order between scalar-coupled 1H-13C nuclear spins. This state has a longer lifetime than the state hyperpolarized at Earth field. The method is simple and cost-efficient and should be applicable to many molecular systems known to exhibit photo-CIDNP, including amino acids and nucleotides.

physics.chem-ph↗