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Early indications for manganese oxidation state changes during photosynthetic oxygen production: a personal account [Review]

机译:光合氧气生产过程中锰氧化态变化的早期迹象:一个个人帐户[查看]

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摘要

One of the major questions yet to be answered in photosynthesis research today is what is the chemical mechanism for the oxidation of water into molecular oxygen. It is well established that an inorganic cluster of four manganese ions and at least one calcium ion form the catalytic core. As the oxidation potential generated by the Photosystem II reaction center is accumulated over the four sequential steps needed to produce O-2, changes in the oxidation state of the catalytic manganese occur, though the formal oxidation states that are involved are still a matter of considerable debate. Much of what is currently known has come from direct measurements of the catalytic manganese using electron paramagnetic resonance (EPR) and X-ray spectroscopy. However, in the early attempts to attack this problem, the catalytic manganese was monitored indirectly by its paramagnetic effect on the nuclear magnetic resonance (NMR) relaxation rates of solvent water protons. In this contribution, a description of the proton relaxation rate phenomenon and its use to indicate manganese oxidation state changes during O-2 production is presented.
机译:今天,在光合作用研究中尚未回答的主要问题之一是将水氧化为分子氧的化学机理是什么。公认的是,由四个锰离子和至少一个钙离子组成的无机簇形成催化核。由于由Photosystem II反应中心产生的氧化电势在产生O-2所需的四个顺序步骤中积累,因此催化锰的氧化态发生了变化,尽管所涉及的形式氧化态仍然是相当大的问题。辩论。当前已知的大部分来自使用电子顺磁共振(EPR)和X射线光谱法对催化锰的直接测量。但是,在解决该问题的早期尝试中,催化性锰是通过其对溶剂水质子的核磁共振(NMR)弛豫速率的顺磁效应间接监测的。在此贡献中,描述了质子弛豫速率现象及其在O-2生产过程中用于指示锰氧化态变化的用途。

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