首页> 外文期刊>Journal of the American Chemical Society >Photochemically induced dynamic nuclear polarization in photosystem I of plants observed by C-13 magic-angle spinning NMR
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Photochemically induced dynamic nuclear polarization in photosystem I of plants observed by C-13 magic-angle spinning NMR

机译:C-13魔角旋转NMR观察到的植物光系统I中光化学诱导的动态核极化

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摘要

Photochemically induced dynamic nuclear polarization (photo-CIDNP) has been observed in photosystem I of spinach by C-13 magic angle spinning solid-state NMR under continuous illumination with white light. An almost complete set of chemical shifts of the aromatic ring carbons of a single Chl a molecule has been obtained which is assigned to the P2-cofactor of the primary electron donor P700. Since all light-induced C-13 NMR signals appear to be emissive, a predominance of the three-spin mixing mechanism over the differential decay mechanism is proposed. The origin of the strong contribution of the three-spin mixing mechanism and the differences with photosystem II are discussed.
机译:在白光连续照射下,通过C-13魔角旋转固态NMR在菠菜的光系统I中观察到了光化学诱导的动态核极化(photo-CIDNP)。已获得单个Chl a分子的芳香环碳的几乎完整的化学位移,该化学位移被分配给一次电子给体P700的P2-辅因子。由于所有光诱导的C-13 NMR信号似乎都是发射的,因此提出了三轴混合机制优于差分衰减机制的优势。讨论了三轴混合机制的强大贡献的起源以及与光系统II的区别。

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