首页> 外文期刊>Journal of the American Chemical Society >INSENSITIVITY OF THE RATE OF DECOMPOSITION OF PEROXYNITRITE TO CHANGES IN VISCOSITY - EVIDENCE AGAINST FREE RADICAL FORMATION
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INSENSITIVITY OF THE RATE OF DECOMPOSITION OF PEROXYNITRITE TO CHANGES IN VISCOSITY - EVIDENCE AGAINST FREE RADICAL FORMATION

机译:过硫酸氢分解速率对粘度变化的敏感性-自由基形成的证据。

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Peroxynitrite is a versatile and important biological oxidant that is produced from the reaction of nitric oxide and superoxide radicals. Two mechanisms have been proposed to rationalize oxidation reactions of peroxynitrite. One assumes that HO-ONO can homolize to form the hydroxyl radical and nitrogen dioxide, and that the hydroxyl radical is the proximate oxidant in peroxynitrite systems. The second argues this homolysis is too slow to occur at ordinary temperatures and suggests an excited species, HOONO*, is the proximate oxidant. If the radical mechanism is correct, then peroxynitrite should disappear more slowly in solvents of higher viscosity. This is true because for free radical initiators undergoing single-bond homolysis: (1) cage return is substantial and more of the cages would return to re-form HO-ONO as the viscosity of the medium increases; and (2) diffusion from the radical cage competes effectively with other cage processes. We have studied the disappearance of peroxynitrite at pH 5 and 7 in buffers with and without dioxane (as a control) or up to 30 wt % of the poly(ethylene glycol) (PEG) polymers, PEG 3350 and PEG 8000. These polyethers produce substantial changes in viscosity, raising the viscosity from about 0.89 to about 17 mPa . s. The rate constant for diffusion should decrease by about 10- to 20-fold as the viscosity increases in this interval, and the rate of diffusion from the solvent cage would be predicted to vary accordingly. However, at pH 5, where most of HOONO is undissociated, no change in the rate of disappearance of peroxynitrite is observed with increasing viscosity. At pH 7, a small increase in the observed rate constant is found, but it is likely due to the greater concentration of the undissociated HOONO in the ether-containing solvents resulting from a pK(a) shift. Thus, we conclude that the viscosity test does not support a free radical mechanism for the unimolecular decomposition of peroxynitrite.
机译:过氧亚硝酸盐是一种多功能的重要生物氧化剂,由一氧化氮和超氧自由基的反应产生。已经提出了两种机制来使过亚硝酸盐的氧化反应合理化。人们认为HO-ONO可以均化形成羟基自由基和二氧化氮,并且羟基自由基是过氧亚硝酸盐体系中最接近的氧化剂。第二种观点认为,这种均解作用太慢而无法在常温下发生,并表明一种被激发的物质HOONO *是最接近的氧化剂。如果自由基机理是正确的,则过亚硝酸盐在粘度较高的溶剂中应更缓慢地消失。的确如此,因为对于自由基引发剂进行单键均质化:(1)笼的回收率很高,并且随着介质粘度的增加,更多的笼将返回以重新形成HO-ONO。 (2)自由基笼的扩散与其他笼过程有效竞争。我们研究了在有和没有二恶烷(作为对照)或不超过30 wt%的聚(乙二醇)(PEG)聚合物,PEG 3350和PEG 8000的缓冲液中,pH 5和7下过亚硝酸盐的消失。这些聚醚产生粘度的实质性变化,将粘度从约0.89提高到约17 mPa。 s。随着粘度在此间隔中的增加,扩散速率常数应减少约10至20倍,并且可以预测从溶剂笼中扩散的速率会相应变化。然而,在pH 5下,大多数HOONO都未解离,随着粘度的增加,过氧亚硝酸盐的消失速率没有变化。在pH值为7时,发现观察到的速率常数略有增加,但这可能是由于pK(a)位移导致含醚的溶剂中未离解的HOONO浓度增加所致。因此,我们得出结论,粘度测试不支持过氧亚硝酸盐单分子分解的自由基机理。

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