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Ahmed H. Zewail

Researcher at California Institute of Technology

Publications -  615
Citations -  43313

Ahmed H. Zewail is an academic researcher from California Institute of Technology. The author has contributed to research in topics: Femtosecond & Excited state. The author has an hindex of 106, co-authored 615 publications receiving 41204 citations. Previous affiliations of Ahmed H. Zewail include University of California, Berkeley & Lawrence Berkeley National Laboratory.

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Femtochemistry: Atomic-Scale Dynamics of the Chemical Bond†

TL;DR: The field of femtochemistry has been studied from a personal perspective, encompassing our research at Caltech and focusing on the evolution of techniques, concepts, and new discoveries.
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Dynamics of water in biological recognition.

TL;DR: Almost all biological macromoleculess proteins and DNAs are inactive in the absence of water, and the role of hydration in enzyme catalysis is well known and has recently been reviewed in a number of publications.
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Four-Dimensional Electron Microscopy

TL;DR: This Review highlights recent developments and inventions made by introducing the fourth dimension of time in electron microscopy, and presents the central concept involved, that of single-electron stroboscopic imaging, which discusses prototypical applications, which include the visualization of complex structures when unfolding on different length and time scales.
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Photon-induced near-field electron microscopy

TL;DR: The observation of the photon-induced near-field effect in ultrafast electron microscopy demonstrates the potential for many applications, including those of direct space-time imaging of localized fields at interfaces and visualization of phenomena related to photonics, plasmonics and nanostructures.
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Biological water at the protein surface: dynamical solvation probed directly with femtosecond resolution.

TL;DR: Results show that hydration at the surface is a dynamical process with two general types of trajectories, those that result from weak interactions with the selected surface site, giving rise to bulk-type solvation, and those that have a stronger interaction, enough to define a rigid water structure, with a solvation time of 38 ps, much slower than that of the bulk.