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首页> 外文期刊>Applied Magnetic Resonance >Action Spectroscopy on Dense Samples of Photosynthetic Reaction Centers of Rhodobacter sphaeroides WT Based on Nanosecond Laser-Flash 13C Photo-CIDNP MAS NMR
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Action Spectroscopy on Dense Samples of Photosynthetic Reaction Centers of Rhodobacter sphaeroides WT Based on Nanosecond Laser-Flash 13C Photo-CIDNP MAS NMR

机译:纳秒激光 13 C Photo-CIDNP MAS NMR的球形球形红细菌WT光合作用中心重样品的活动光谱

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摘要

Photochemically induced dynamic nuclear polarization magic-angle spinning nuclear magnetic resonance (photo-CIDNP MAS NMR) allows for the investigation of the electronic structure of the photochemical machinery of photosynthetic reaction centers (RCs) at atomic resolution. For such experiments, either continuous radiation from white xenon lamps or green laser pulses are applied to optically dense samples. In order to explore their optical properties, optically thick samples of isolated and quinone-removed RCs of the purple bacteria of Rhodobacter sphaeroides wild type are studied by nanosecond laser-flash 13C photo-CIDNP MAS NMR using excitation wavelengths between 720 and 940 nm. Action spectra of both the transient nuclear polarization as well as the nuclear hyperpolarization, remaining in the electronic ground state at the end of the photocycle, are obtained. It is shown that the signal intensity is limited by the amount of accessible RCs and that the different mechanisms of the photo-CIDNP production rely on the same photophysical origin, which is the photocycle induced by one single photon.
机译:光化学诱导的动态核极化魔角旋转核磁共振(photo-CIDNP MAS NMR)允许以原子分辨率研究光合反应中心(RCs)的光化学机械的电子结构。对于此类实验,可以将来自白色氙气灯的连续辐射或绿色激光脉冲施加到光密度较高的样品上。为了探索它们的光学性质,使用纳秒激光 13 C photo-CIDNP MAS NMR激发,研究了球形球形红细菌紫色细菌的分离和醌去除的RC的光学厚度样品。波长介于720和940 nm之间。获得瞬态核极化和核超极化的作用谱,它们在光循环结束时仍保持在电子基态。结果表明,信号强度受到可访问的RC数量的限制,并且光CIDNP产生的不同机制依赖于相同的光物理起源,即一个单一光子诱导的光循环。

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