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91.
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Ridley AR Stewart AI Adamczyk K Ghosh HN Kerkeni B Guo ZX Nibbering ET Pickett CJ Hunt NT 《Inorganic chemistry》2008,47(17):7453-7455
Ultraviolet (UV) photolysis of (mu-S(CH 2) 3S)Fe 2(CO) 6 ( 1), a model compound of the Fe-hydrogenase enzyme system, has been carried out. When ultrafast UV-pump infrared (IR)-probe spectroscopy, steady-state Fourier transform IR spectroscopic methods, and density functional theory simulations are employed, it has been determined that irradiation of 1 in an alkane solution at 350 nm leads to the formation of two isomers of the 16-electron complex (mu-S(CH 2) 3S)Fe 2(CO) 5 within 50 ps with evidence of a weakly associated solvent adduct complex. 1 is subsequently recovered on timescales covering several minutes. These studies constitute the first attempt to study the photochemistry and reactivity of these enzyme active site models in solution following carbonyl ligand photolysis. 相似文献
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In this article, we introduce the concept of lacunary statistical convergence of order α of real number sequences and give some inclusion relations between the sets of lacunary statistical convergence of order α and strong Nαθ(p)-summability. Furthermore, some relations between the spaces Nαθ(p) and Sαθare examined. 相似文献
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Łukasz Szyc Ming Yang Erik T. J. Nibbering Dr. Thomas Elsaesser Prof. Dr. 《Angewandte Chemie (International ed. in English)》2010,49(21):3598-3610
Biochemical processes occur mainly in aqueous environments, where interactions with water molecules play a key role for both the structure and function of biomolecules. Deoxyribonucleic acid (DNA), the basic carrier of genetic information, is characterized by an equilibrium double helix structure which is held together by intermolecular hydrogen bonds between base pairs and hydrated by an environment of water molecules with fluctuating hydrogen bonds. Basic vibrational motions of hydrated DNA and the fastest changes in the DNA–water interactions and hydration geometries occur in less than 1 ps. These processes can be accessed by mapping the vibrational dynamics of DNA and water in a time‐resolved way by nonlinear ultrafast vibrational spectroscopy. Recent studies provide a detailed understanding of DNA vibrations and their dynamics, and give insight into nonequilibrium properties and structures of hydrated DNA. 相似文献
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Ghosh HN Adamczyk K Verma S Dreyer J Nibbering ET 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(16):4930-4937
Using ultrafast fluorescence upconversion and mid-infrared spectroscopy, we explore the role of hydrogen bonds in the photoinduced electron transfer (ET) between 9-fluorenone (FLU) and the solvents trimethylamine (TEA) and dimethylamine (DEA). FLU shows hydrogen-bond dynamics in the methanol solvent upon photoexcitation, and similar effects may be anticipated when using DEA, whereas no hydrogen bonds can occur in TEA. Photoexcitation of the electron-acceptor dye molecule FLU with a 400?nm pump pulse induces ultrafast ET from the amine solvents, which is followed by 100?fs IR probe pulses as well as fluorescence upconversion, monitoring the time evolution of marker bands of the FLU S(1) state and the FLU radical anion, and an overtone band of the amine solvent, marking the transient generation of the amine radical cation. A comparison of the experimentally determined forward charge-separation and backward charge-recombination rates for the FLU-TEA and FLU-DEA reaction systems with the driving-force dependencies calculated for the forward and backward ET rates reveals that additional degrees of freedom determine the ET reaction dynamics for the FLU-DEA system. We suggest that hydrogen bonding between the DEA molecules plays a key role in this behaviour. 相似文献
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′ -hydroxy-5′-methylphenyl)-benzotriazole.
Received: 2 June 1998/Revised version: 31 July 1998 相似文献