Time-resolved resonance Raman spectroscopy of the carbonate radical

R. Bisby, Steven A. Johnson, A. Parker, S. Tavender
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引用次数: 29

Abstract

The literature contains conflicting evidence regarding the protonation state of the carbonate radical, a species which now appears to be of biological significance. The time-resolved resonance Raman spectrum of CO3- has been observed. The radical was produced by oxidation of bicarbonate and carbonate using sulfate radicals at pH values from 7.5 to 12.3. The resonance Raman spectrum was found to be invariant with pH and contains a strongly polarised and intense band at 1062 cm-1. The spectrum is consistent with the radical having C2v symmetry, indicating some distortion from the predicted D3h structure. The data suggest that the carbonate radical (CO3-) formed by one-electron oxidation of bicarbonate and carbonate does not undergo protonation to the conjugate acid, HCO3, as previously suggested with a pKa of 9.6. Some biochemical consequences of this are discussed.
碳酸盐自由基的时间分辨共振拉曼光谱
关于碳酸盐自由基的质子化状态,文献中包含了相互矛盾的证据,这一物种现在似乎具有生物学意义。研究了CO3-的时间分辨共振拉曼光谱。该自由基是在pH值为7.5 ~ 12.3的硫酸盐自由基作用下,由碳酸氢盐和碳酸盐氧化生成的。发现共振拉曼光谱随pH值不变,并在1062 cm-1处包含一个强极化和强波段。光谱与C2v对称的自由基一致,表明与预测的D3h结构有一定的畸变。数据表明,碳酸氢盐和碳酸盐的单电子氧化形成的碳酸盐自由基(CO3-)不会像先前提出的pKa为9.6那样质子化成共轭酸HCO3。讨论了这一过程的一些生化后果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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