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Trityl-Aryl-Nitroxide-Based Genuinely g-Engineered Biradicals, As Studied by Dynamic Nuclear Polarization, Multifrequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy, and Quantum Chemical Calculations. / Sato, Kazunobu; Hirao, Rei; Timofeev, Ivan и др.
в: Journal of Physical Chemistry A, Том 123, № 34, 27.07.2019, стр. 7507-7517.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Trityl-Aryl-Nitroxide-Based Genuinely g-Engineered Biradicals, As Studied by Dynamic Nuclear Polarization, Multifrequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy, and Quantum Chemical Calculations
AU - Sato, Kazunobu
AU - Hirao, Rei
AU - Timofeev, Ivan
AU - Krumkacheva, Olesya
AU - Zaytseva, Elena
AU - Rogozhnikova, Olga
AU - Tormyshev, Victor M.
AU - Trukhin, Dmitry
AU - Bagryanskaya, Elena
AU - Gutmann, Torsten
AU - Klimavicius, Vytautas
AU - Buntkowsky, Gerd
AU - Sugisaki, Kenji
AU - Nakazawa, Shigeaki
AU - Matsuoka, Hideto
AU - Toyota, Kazuo
AU - Shiomi, Daisuke
AU - Takui, Takeji
N1 - Publisher Copyright: Copyright © 2019 American Chemical Society.
PY - 2019/7/27
Y1 - 2019/7/27
N2 - Trityl and nitroxide radicals are connected by π-topologically controlled aryl linkers, generating genuinely g-engineered biradicals. They serve as a typical model for biradicals in which the exchange (J) and hyperfine interactions compete with the g-difference electronic Zeeman interactions. The magnetic properties underlying the biradical spin Hamiltonian for solution, including J's, have been determined by multifrequency CW-ESR and 1H ENDOR spectroscopy and compared with those obtained by quantum chemical calculations. The experimental J values were in good agreement with the quantum chemical calculations. The g-engineered biradicals have been tested as a prototype for AWG (Arbitrary Wave Generator)-based spin manipulation techniques, which enable GRAPE (GRAdient Pulse Engineering) microwave control of spins in molecular magnetic resonance spectroscopy for use in molecular spin quantum computers, demonstrating efficient signal enhancement of specific weakened hyperfine signals. Dynamic nuclear polarization (DNP) effects of the biradicals for 400 MHz nuclear magnetic resonance signal enhancement have been examined, giving efficiency factors of 30 for 1H and 27.8 for 13C nuclei. The marked DNP results show the feasibility of these biradicals for hyperpolarization.
AB - Trityl and nitroxide radicals are connected by π-topologically controlled aryl linkers, generating genuinely g-engineered biradicals. They serve as a typical model for biradicals in which the exchange (J) and hyperfine interactions compete with the g-difference electronic Zeeman interactions. The magnetic properties underlying the biradical spin Hamiltonian for solution, including J's, have been determined by multifrequency CW-ESR and 1H ENDOR spectroscopy and compared with those obtained by quantum chemical calculations. The experimental J values were in good agreement with the quantum chemical calculations. The g-engineered biradicals have been tested as a prototype for AWG (Arbitrary Wave Generator)-based spin manipulation techniques, which enable GRAPE (GRAdient Pulse Engineering) microwave control of spins in molecular magnetic resonance spectroscopy for use in molecular spin quantum computers, demonstrating efficient signal enhancement of specific weakened hyperfine signals. Dynamic nuclear polarization (DNP) effects of the biradicals for 400 MHz nuclear magnetic resonance signal enhancement have been examined, giving efficiency factors of 30 for 1H and 27.8 for 13C nuclei. The marked DNP results show the feasibility of these biradicals for hyperpolarization.
KW - SPIN NUTATION SPECTROSCOPY
KW - ELECTRONIC-STRUCTURES
KW - ENHANCED NMR
KW - RESONANCE
KW - EFFICIENT
KW - EXCHANGE
KW - EPR
KW - DIPOLAR
KW - ENDOR
KW - TRIRADICALS
UR - http://www.scopus.com/inward/record.url?scp=85071679850&partnerID=8YFLogxK
U2 - 10.1021/acs.jpca.9b07169
DO - 10.1021/acs.jpca.9b07169
M3 - Article
C2 - 31373818
AN - SCOPUS:85071679850
VL - 123
SP - 7507
EP - 7517
JO - Journal of Physical Chemistry A
JF - Journal of Physical Chemistry A
SN - 1089-5639
IS - 34
ER -
ID: 21464881