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Kinetics of rapid covalent bond formation of aniline with humic acid: ESR investigations with nitroxide spin labels

机译:苯胺与腐殖酸快速共价键形成的动力学:使用一氧化氮自旋标记的ESR研究

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摘要

ABSTRACTudThe bioavailability of many soil contaminants depends on their interaction with the soil organic matter. The paper presents a new approach of using stable paramagnetic spin labels for investigating the kinetics of covalent binding of specific xenobiotic functional groups with humic acids, a major organic matter fraction. Leonardite humic acid (LHA) was incubated with the nitroxide spin labels amino-TEMPO (4-amino-2,2,6,6-Tetramethylpiperidin-1-oxyl) and anilino-NO (2,5,5-Trimethyl-2-(3-aminophenyl)pyrrolidin-1-oxyl), respectively, which contain an aliphatic or aromatic functionality susceptible to interaction with LHA. Electron spin resonance (ESR) spectra of LHA samples without and with the enzyme laccase were recorded at X-band frequency (9.43 GHz) at room temperature and neutral pH. Binding was detected by a pronounced broadening of the spectral lines after incubation of LHA for both spin labels. The development of a broad signal component in the spectrum of anilino-NO indicated the immobilization due to strong binding of the aniline group. The reorientational correlation time of bound anilino-NO is more than two orders of magnitude greater than that of the free label. The ratio of the amount of bound to the unbound species was used to determine the kinetics of the covalent bond formation. Reaction rate constants of 0.16 min-1 and 0.01 min-1 were determined corresponding to half-times of 4.3 min and 69.3 min, respectively. Treatment of LHA with laccase enhanced the amount of the reacting anilino-NO species by a factor of 7.6, but left the reaction rate unaltered. Oxidative radical coupling was excluded by using the spin trap agent n-tert-butyl-alpha-phenylnitrone. ud
机译:摘要 ud许多土壤污染物的生物利用度取决于它们与土壤有机质的相互作用。本文提出了一种使用稳定的顺磁性自旋标记物研究特定异种生物官能团与腐殖酸(一种主要的有机物组分)共价结合的动力学的新方法。将绿矾土腐殖酸(LHA)与一氧化氮旋转标记氨基-TEMPO(4-氨基-2,2,6,6-四甲基哌啶-1-氧基)和苯胺基-NO(2,5,5-三甲基-2- (3-氨基苯基)吡咯烷-1-氧基)分别含有易于与LHA相互作用的脂族或芳族官能团。在室温和中性pH的X波段频率(9.43 GHz)下记录了不使用和使用酶漆酶的LHA样品的电子自旋共振(ESR)光谱。在两种自旋标记物孵育LHA后,通过显着加宽谱线来检测结合。由于苯胺基团的强结合,苯胺基-NO谱中宽信号成分的发展表明了固定化。结合的苯胺基-NO的重组相关时间比自由标记的重组相关时间大两个数量级。结合的量与未结合的种类的比率用于确定共价键形成的动力学。确定的反应速率常数为0.16 min-1和0.01 min-1,分别对应于4.3分钟和69.3分钟的半衰期。用漆酶处理LHA可将反应性Anilino-NO种类的量提高7.6倍,但反应速率保持不变。通过使用自旋捕集剂n-叔丁基-α-苯基硝基消除了氧化性自由基偶联。 ud

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