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Femtosecond relaxation processes in Rhodobacter sphaeroides reaction centers

机译:乳头杆菌的飞秒放松过程反应中心

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Energy relaxation was studied with difference femtosecond spectroscopy in reaction centers of the YM210L mutant of the purple photosynthetic bacterium Rhodobacter sphaeroides at low temperature (90 K). A dynamical long-wavelength shift of stimulated emission of the excited state of the bacteriochlorophyll dimer P was found, which starts simultaneously with P* formation and is accompanied by a change in the spectral shape of this emission. The characteristic value of this shift was about 30 nm, and the characteristic time about 200 fs. Difference kinetics Delta A measured at fixed wavelengths demonstrate the femtosecond shift of the P* stimulated emission appearing as a dependence of these kinetics on wavelength. We found that the reported long-wavelength shift can be explained in terms of electron-vibrational relaxation of the P* excited state with time constants of vibrational and electronic relaxation of 100 and 50 fs, respectively. Alternative mechanisms of the dynamical shift of the P* stimulated emission spectrum are also discussed in terms of energy redistribution between vibrational modes or coherent excitation of the modes.
机译:在低温(90k)的紫色光合细菌乳菌斯氏菌植物的YM210L突变体的反应中心中研究了能量松弛。发现了刺激发射的抗菌氯基二聚体P的激发发射的动态长波长偏移,其与P *形成同时开始,并伴随着该发射的光谱形状的变化。该移位的特征值为约30nm,特征时间约为200 fs。在固定波长下测量的差异动力学ΔA证明了P *刺激发射的飞秒移位作为这些动力学对波长的依赖性。我们发现报告的长波长偏移可以分别在P *激发状态的电子振动松弛方面解释,其时间常数分别为100和50 fs的振动和​​电子松弛的时间常数。在振动模式之间的能量再分布或模式的相干激发方面还讨论了P *刺激发射光谱的动态移位的替代机制。

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