一氧化氮介导的自由基聚合
化学
激进的
电子顺磁共振
极化(电化学)
未成对电子
核磁共振
光化学
聚合物
物理化学
有机化学
物理
共聚物
自由基聚合
作者
Jakob A. Meckes,Zachary W. Schroeder,Diganta Sarkar,Riley W. Hooper,Clara E. Faraday-Smith,Alex Brown,Rik R. Tykwinski,Vladimir K. Michaelis
摘要
High-field dynamic nuclear polarization nuclear magnetic resonance (DNP NMR) spectroscopy transfers polarization from unpaired electrons in polarizing agents to nuclei of interest to boost NMR sensitivity. Verdazyl biradicals are a promising choice as polarizing agents because they have been found to generate narrower electron paramagnetic resonance (EPR) signals compared to nitroxide biradicals; an advantageous characteristic for high-field DNP when operating above 400 MHz/263 GHz. The use of verdazyl radicals as DNP polarizing agents has been very limited to date, yet, recent numerical simulations have predicted that verdazyl-nitroxide hybrid biradicals could be more effective polarizing agents than nitroxide-nitroxide biradicals. Herein, the syntheses of a series of verdazyl mono- and biradicals, as well as verdazyl-nitroxide biradicals are described. These radicals were examined in high-field DNP NMR experiments (600 MHz/395 GHz), by measuring 1H signal enhancements directly and through 13C{1H} cross-polarization experiments. X-band EPR, 1H DNP field profiles, and experiments to determine the nuclear build-up times were performed for verdazyl-nitroxide biradicals VerTEMPol and VerTEKol. These hybrid biradicals provide enhancements of up to 100-fold increased signal intensities (i.e., representing >104-fold time savings), approximately four times higher than that of the nitroxide biradical TEKPol, a commonly used polarizing agent in the field.
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