首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Ultrafast XANES Monitors Femtosecond Sequential Structural Evolution in Photoexcited Coenzyme B-12
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Ultrafast XANES Monitors Femtosecond Sequential Structural Evolution in Photoexcited Coenzyme B-12

机译:超快Xanes在光透明辅酶B-12中监控飞秒顺序结构演进

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摘要

Polarized X-ray absorption near-edge structure (XANES) at the Co K-edge and broadband UV-vis transient absorption are used to monitor the sequential evolution of the excited-state structure of coenzyme B-12 (adenosylcobalamin) over the first picosecond following excitation. The initial state is characterized by sub -100 fs sequential changes around the central cobalt. These are polarized first in the y-direction orthogonal to the transition dipole and 50 fs later in the x-direction along the transition dipole. Expansion of the axial bonds follows on a ca. 200 fs time scale as the molecule moves out of the Franck-Condon active region of the potential energy surface. On the same 200 fs time scale there are electronic changes that result in the loss of stimulated emission and the appearance of a strong absorption at 340 nm. These measurements provide a cobalt-centered movie of the excited molecule as it evolves to the local excited-state minimum.
机译:Co K-Edge和宽带UV-VI瞬态吸收的偏振X射线吸收近边缘结构(XANES)用于监测第一个PICOSECOND上辅酶B-12(腺苷钴胺素)的激发态结构的顺序演变 兴奋之后。 初始状态的特征在于Central钴周围的Sub -100 FS顺序变化。 它们在沿y方向上偏振于过渡偶极子和50fs在沿横向偶极子的X方向上偏振。 轴向键的膨胀在CA上遵循。 当分子从潜在能量表面的Franck-Condon有源区移出时,200 FS时间尺度。 在同一200 FS时间尺度上,有电子变化导致受刺激的排放损失以及340nm处的强吸收的外观。 这些测量提供了兴奋分子的钴中心电影,因为它发展到局部兴奋状态最小值。

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