Sato Kazunobu, Hirao Rei, Timofeev Ivan, Krumkacheva Olesya, Zaytseva Elena, Rogozhnikova Olga, Tormyshev Victor M, Trukhin Dmitry, Bagryanskaya Elena, Gutmann Torsten, Klimavicius Vytautas, Buntkowsky Gerd, Sugisaki Kenji, Nakazawa Shigeaki, Matsuoka Hideto, Toyota Kazuo, Shiomi Daisuke, Takui Takeji
Department of Chemistry and Molecular Materials Science, Graduate School of Science , Osaka City University , 3-3-138 Sugimoto , Sumiyoshi-ku, Osaka 558-8585 , Japan.
N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry , Novosibirsk 630090 , Russia.
J Phys Chem A. 2019 Aug 29;123(34):7507-7517. doi: 10.1021/acs.jpca.9b07169. Epub 2019 Aug 16.
Trityl and nitroxide radicals are connected by π-topologically controlled aryl linkers, generating genuinely -engineered biradicals. They serve as a typical model for biradicals in which the exchange () and hyperfine interactions compete with the -difference electronic Zeeman interactions. The magnetic properties underlying the biradical spin Hamiltonian for solution, including 's, have been determined by multifrequency CW-ESR and H ENDOR spectroscopy and compared with those obtained by quantum chemical calculations. The experimental values were in good agreement with the quantum chemical calculations. The -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 H and 27.8 for C nuclei. The marked DNP results show the feasibility of these biradicals for hyperpolarization.
三芳基甲基自由基和氮氧化物自由基通过π拓扑控制的芳基连接基相连,生成真正经过设计的双自由基。它们是双自由基的典型模型,其中交换()和超精细相互作用与 - 差分电子塞曼相互作用相互竞争。通过多频连续波电子自旋共振(CW - ESR)和高分辨电子核双共振(H ENDOR)光谱确定了溶液中双自由基自旋哈密顿量的磁性质,包括 的磁性质,并与量子化学计算得到的结果进行了比较。实验值与量子化学计算结果吻合良好。这些经过设计的双自由基已作为基于任意波形发生器(AWG)的自旋操纵技术的原型进行了测试,该技术能够在分子磁共振光谱中对自旋进行梯度脉冲工程(GRAPE)微波控制,用于分子自旋量子计算机,证明了特定减弱超精细信号的有效信号增强。已经研究了双自由基对400 MHz核磁共振信号增强的动态核极化(DNP)效应,得到氢核的效率因子为30,碳核的效率因子为27.8。显著的DNP结果表明这些双自由基用于超极化的可行性。