Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State

Bibliographische Detailangaben
Parent link:Journal of the American Chemical Society (JACS)
Vol. 143, iss. 21.— 2021.— [P. 8164–8176]
Körperschaft: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
Weitere Verfasser: Tretjyakov E. V. Evgeny Viktorovich, Petunin P. V. Pavel Vasilievich, Zhivetjeva S. I. Svetlana Ivanovna, Gorbunov D. E. Dmitry Evgenjevich, Gritsan N. P. Nina Petrovna, Fedin M. V. Matvey Vladimirovich, Stas D. V. Dmitry Vladimirovich, Samoylova R. I. Rimma Ivanovna, Bagryanskaya I. Yu. Irina Yurjevna, Shundrina I. K. Inna Kazimirovna, Bogomyakov A. S. Artem Stepanovich, Kazantsev M. S. Maksim Sergeevich, Postnikov P. S. Pavel Sergeevich, Trusova M. E. Marina Evgenievna, Ovcharenko V. I. Viktor Ivanovich
Zusammenfassung:Title screen
Thermally resistant air-stable organic triradicals with a quartet ground state and a large energy gap between spin states are still unique compounds. In this work, we succeeded to design and prepare the first highly stable triradical, consisting of oxoverdazyl and nitronyl nitroxide radical fragments, with a quartet ground state. The triradical and its diradical precursor were synthesized via a palladium-catalyzed cross-coupling reaction of diiodoverdazyl with nitronyl nitroxide-2-ide gold(I) complex. Both paramagnetic compounds were fully characterized by single-crystal X-ray diffraction analysis, superconducting quantum interference device magnetometry, EPR spectroscopy in various matrices, and cyclic voltammetry. In the diradical, the verdazyl and nitronyl nitroxide centers demonstrated full reversibility of redox process, while for the triradical, the electrochemical reduction and oxidation proceed at practically the same redox potentials, but become quasi-reversible. A series of high-level CASSCF/NEVPT2 calculations was performed to predict inter- and intramolecular exchange interactions in crystals of di- and triradicals and to establish their magnetic motifs. Based on the predicted magnetic motifs, the temperature dependences of the magnetic susceptibility were analyzed, and the singlet-triplet (135±10 cm-1) and doublet-quartet (17±2 and 152±19 cm-1) splitting was found to be moderate. Unique high stability of synthesized verdazyl-nitronylnitroxide triradical opens new perspectives for further functionalization and design of high-spin systems with four or more spins.
Режим доступа: по договору с организацией-держателем ресурса
Sprache:Englisch
Veröffentlicht: 2021
Schlagworte:
Online-Zugang:https://pubs.acs.org/doi/10.1021/jacs.1c02938?goto=supporting-info
Format: Elektronisch Buchkapitel
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=666286

MARC

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200 1 |a Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State  |f E. V. Tretjyakov, P. V. Petunin, S. I. Zhivetjeva [et al.] 
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300 |a Title screen 
330 |a Thermally resistant air-stable organic triradicals with a quartet ground state and a large energy gap between spin states are still unique compounds. In this work, we succeeded to design and prepare the first highly stable triradical, consisting of oxoverdazyl and nitronyl nitroxide radical fragments, with a quartet ground state. The triradical and its diradical precursor were synthesized via a palladium-catalyzed cross-coupling reaction of diiodoverdazyl with nitronyl nitroxide-2-ide gold(I) complex. Both paramagnetic compounds were fully characterized by single-crystal X-ray diffraction analysis, superconducting quantum interference device magnetometry, EPR spectroscopy in various matrices, and cyclic voltammetry. In the diradical, the verdazyl and nitronyl nitroxide centers demonstrated full reversibility of redox process, while for the triradical, the electrochemical reduction and oxidation proceed at practically the same redox potentials, but become quasi-reversible. A series of high-level CASSCF/NEVPT2 calculations was performed to predict inter- and intramolecular exchange interactions in crystals of di- and triradicals and to establish their magnetic motifs. Based on the predicted magnetic motifs, the temperature dependences of the magnetic susceptibility were analyzed, and the singlet-triplet (135±10 cm-1) and doublet-quartet (17±2 and 152±19 cm-1) splitting was found to be moderate. Unique high stability of synthesized verdazyl-nitronylnitroxide triradical opens new perspectives for further functionalization and design of high-spin systems with four or more spins. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Journal of the American Chemical Society (JACS) 
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701 1 |a Tretjyakov  |b E. V.  |g Evgeny Viktorovich 
701 1 |a Petunin  |b P. V.  |c chemist  |c Associate Professor of Tomsk Polytechnic University, Candidate of Chemical Sciences  |f 1982-  |g Pavel Vasilievich  |3 (RuTPU)RU\TPU\pers\36904  |9 19933 
701 1 |a Zhivetjeva  |b S. I.  |g Svetlana Ivanovna 
701 1 |a Gorbunov  |b D. E.  |g Dmitry Evgenjevich 
701 1 |a Gritsan  |b N. P.  |g Nina Petrovna 
701 1 |a Fedin  |b M. V.  |g Matvey Vladimirovich 
701 1 |a Stas  |b D. V.  |g Dmitry Vladimirovich 
701 1 |a Samoylova  |b R. I.  |g Rimma Ivanovna 
701 1 |a Bagryanskaya  |b I. Yu.  |g Irina Yurjevna 
701 1 |a Shundrina  |b I. K.  |g Inna Kazimirovna 
701 1 |a Bogomyakov  |b A. S.  |g Artem Stepanovich 
701 1 |a Kazantsev  |b M. S.  |g Maksim Sergeevich 
701 1 |a Postnikov  |b P. S.  |c organic chemist  |c Associate Professor of Tomsk Polytechnic University, Candidate of chemical sciences  |f 1984-  |g Pavel Sergeevich  |3 (RuTPU)RU\TPU\pers\31287 
701 1 |a Trusova  |b M. E.  |c organic chemist  |c Associate professor of Tomsk Polytechnic University, Candidate of chemical sciences  |f 1982-  |g Marina Evgenievna  |3 (RuTPU)RU\TPU\pers\31823  |9 15918 
701 1 |a Ovcharenko  |b V. I.  |g Viktor Ivanovich 
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