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Nonpentacene Polarizing Agents with Improved Air Stability for Triplet Dynamic Nuclear Polarization at Room Temperature

机译:具有改善的空气稳定性,在室温下改善了三联动态核极化的空气稳定性

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摘要

Triplet dynamic nuclear polarization (triplet-DNP), a method to enhance nuclear magnetic resonance (NMR) and magnetic resonance imaging (MRI) sensitivity using photoexcited triplet electrons, has great potential to hyperpolarize nuclear spins at room temperature. Since the first report of room-temperature triplet-DNP in 1990, pentacene has been the only and best option of triplet polarizing agent. However, the poor air stability of pentacene has severely limited the applicability of triplet-DNP. We report the first example of polarizing agents with significant air stability as well as high polarizing ability comparable to pentacene. The introduction of electron-withdrawing diaza-substitution to pentacene and tetracene reduces the lowest unoccupied molecular orbital level and endows much improved stability under the ambient conditions. Importantly, the diaza-substituted pentacene and tetracene offer similar, or even slightly better, H-1 NMR signal enhancement compared with pentacene in the prototypical triplet-DNP test using p-terphenyl crystals. This work removes one of the largest obstacles toward the application of triplet-DNP for the hyperpolarization of biological molecules.
机译:三重态动态核偏振(Triplet-DNP),使用光透射三重电子的增强核磁共振(NMR)和磁共振成像(MRI)灵敏度的方法,对室温过度极化核旋转具有很大的潜力。自1990年第一份房间温度TriLINL-DNP报告以来,五星期一直是三重态偏振剂的唯一和最佳选择。然而,五烯烯的空气稳定性差异严重限制了三重药-DNP的适用性。我们报道了具有显着的空气稳定性的偏振剂的第一例以及与五苯相当的高偏振能力。将吸电子的Diaza取代引入五烯和四环的替代降低了最低的未占用的分子轨道水平,赋予环境条件下的稳定性大大提高。重要的是,与使用p-三苯基-DNP试验中的五苯基晶体中的五苯二烯烯相比,DiaZa取代的五烯和四烯和四环发出类似,甚至略微更好,H-1 NMR信号增强。这项工作消除了朝向生物分子超极化的三重态-DNP应用的最大障碍之一。

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    Kyushu Univ CMS Grad Sch Engn Dept Chem &

    Biochem Nishi Ku 744 Moto Oka Fukuoka Fukuoka 8190395 Japan;

    Kyushu Univ CMS Grad Sch Engn Dept Chem &

    Biochem Nishi Ku 744 Moto Oka Fukuoka Fukuoka 8190395 Japan;

    RIKEN RIKEN Nishina Ctr Accelerator Based Sci Cluster Pioneering Res 2-1 Hirosawa Wako Saitama 3510198 Japan;

    RIKEN RIKEN Nishina Ctr Accelerator Based Sci Cluster Pioneering Res 2-1 Hirosawa Wako Saitama 3510198 Japan;

    Kyushu Univ CMS Grad Sch Engn Dept Chem &

    Biochem Nishi Ku 744 Moto Oka Fukuoka Fukuoka 8190395 Japan;

    Kyushu Univ CMS Grad Sch Engn Dept Chem &

    Biochem Nishi Ku 744 Moto Oka Fukuoka Fukuoka 8190395 Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 物理化学(理论化学)、化学物理学;
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