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Arthur E. Bragg

Researcher at Johns Hopkins University

Publications -  64
Citations -  2993

Arthur E. Bragg is an academic researcher from Johns Hopkins University. The author has contributed to research in topics: Excited state & Relaxation (NMR). The author has an hindex of 26, co-authored 60 publications receiving 2738 citations. Previous affiliations of Arthur E. Bragg include University of California, Los Angeles & Lawrence Berkeley National Laboratory.

Papers
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Femtosecond time-resolved photoelectron spectroscopy.

TL;DR: Femtosecond time-resolved or wave packet methods offer a view complementary to the usual spectroscopic approach and often yield a physically intuitive picture in discerning underlying dynamics.
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Observation of large water-cluster anions with surface-bound excess electrons.

TL;DR: In this article, the authors used photoelectron imaging to characterize a class of (H2O)n− and (D2On−)n-cluster anions with vertical binding energies that are significantly lower than those previously recorded.
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Hydrated Electron Dynamics: From Clusters to Bulk

TL;DR: The results support the “nonadiabatic relaxation” mechanism for the bulk hydrated electron mechanism and support the internal conversion lifetime of the p-state population decay with concomitant s-state repopulation.
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High Conductivity and Electron-Transfer Validation in an n-Type Fluoride-Anion-Doped Polymer for Thermoelectrics in Air.

TL;DR: The result shows that using solution-processable small-anion salts such as TBAF as an n-dopant of organic conjugated polymers possessing lower LUMO (lowest unoccupied molecular orbital), less than -4.2 eV) can open new opportunities toward high-performance air-stable solution- Processable n-type thermoelectric (TE) conjugate polymers.
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Aminofluorination of Cyclopropanes: A Multifold Approach through a Common, Catalytically Generated Intermediate

TL;DR: Calculations suggest that solvent may play an important role in the cyclopropane ring-opening step, and transient-absorption experiments have allowed direct spectroscopic observation of radical ion intermediates and have provided kinetic support for chain propagation.