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一氧化氮与硫化氢、醇类和硫醇反应非常迅速,生成HNO:修订后的速率常数。

Nitric Oxide Reacts Very Fast with Hydrogen Sulfide, Alcohols, and Thiols to Produce HNO: Revised Rate Constants.

作者信息

Neuman Nicolas I, Venâncio Mateus F, Rocha Willian R, Bikiel Damian E, Suárez Sebastián A, Doctorovich Fabio

机构信息

Instituto de Desarrollo Tecnológico para la Industria Química, INTEC, UNL-CONICET, Paraje El Pozo, Santa Fe 3000, Argentina.

Institut für Anorganische Chemie, Universität Stuttgart, Stuttgart D-70569, Germany.

出版信息

Inorg Chem. 2021 Nov 1;60(21):15997-16007. doi: 10.1021/acs.inorgchem.1c01061. Epub 2021 Aug 27.

Abstract

The chemical reactivity of NO and its role in several biological processes seem well established. Despite this, the chemical reduction of NO toward HNO has been historically discarded, mainly because of the negative reduction potential of NO. However, this value and its implications are nowadays under revision. The last reported redox potential, '(NO,H/HNO), at micromolar and picomolar concentrations of NO and HNO, respectively, is between -0.3 and 0 V at pH 7.4. This potential implies that the one-electron-reduction process for NO is feasible under biological conditions and could be promoted by well-known biological reductants with reduction potentials of around -0.3 to -0.5 V. Moreover, the biologically compatible chemical reduction of NO (nonenzymatic), like direct routes to HNO by alkylamines, aromatic and pseudoaromatic alcohols, thiols, and hydrogen sulfide, has been extensively explored by our group during the past decade. The aim of this work is to use a kinetic modeling approach to analyze electrochemical HNO measurements and to report for the first-time direct reaction rate constants between NO and moderate reducing agents, producing HNO. These values are between 5 and 30 times higher than the previously reported values. On the other hand, we also showed that reaction through successive attack by two NO molecules to biologically compatible compounds could produce HNO. After over 3 decades of intense research, the NO chemistry is still there, ready to be discovered.

摘要

一氧化氮(NO)的化学反应性及其在若干生物过程中的作用似乎已得到充分证实。尽管如此,NO向亚硝酸(HNO)的化学还原在历史上一直被摒弃,主要原因是NO的负还原电位。然而,如今这一数值及其影响正在重新审视之中。最近报道的分别在微摩尔和皮摩尔浓度的NO和HNO条件下的氧化还原电位‘(NO,H/HNO),在pH 7.4时介于-0.3至0 V之间。这一电位意味着NO的单电子还原过程在生物条件下是可行的,并且可以由还原电位约为-0.3至-0.5 V的著名生物还原剂促进。此外,在过去十年中,我们小组广泛探索了NO的生物相容性化学还原(非酶促),如烷基胺、芳香族和准芳香族醇、硫醇以及硫化氢将NO直接转化为HNO的途径。这项工作的目的是使用动力学建模方法来分析电化学HNO测量结果,并首次报告NO与产生HNO的适度还原剂之间的直接反应速率常数。这些数值比先前报道的值高出5至30倍。另一方面,我们还表明,两个NO分子连续攻击生物相容性化合物的反应可以产生HNO。经过三十多年的深入研究,NO化学仍有待发现。

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