Results 201 to 210 of about 14,840 (242)
Modeling Photodissociation: Quantum Dynamics Simulations of Methanol. [PDF]
Cigrang LLE, Worth GA.
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Synthesis, light-controlled antibacterial and anti-tumor activities of Ginkgo biloba leaves polyprenols-based polypyridine metal complexes. [PDF]
Zhang C, Yuan H, Shen H, Ye J, Wang C.
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Ultrafast photochemical processes in 1,2-dichloroethene measured with a universal XUV probe.
McGhee HG+10 more
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Photodissociation dynamics of pyridine [PDF]
Photodissociation of pyridine, 2,6-d2-pyridine, and d5-pyridine at 193 and 248nm was investigated separately using multimass ion imaging techniques. Six dissociation channels were observed at 193nm, including C5NH5→C5NH4+H (10%) and five ring opening dissociation channels, C5NH5→C4H4+HCN, C5NH5→C3H3+C2NH2, C5NH5→C2H4+C3NH, C5NH5→C4NH2+CH3 (14%), and ...
Yuri A. Dyakov+10 more
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Physical Chemistry Chemical Physics, 2007
We investigate the photochemistry and photodissociation dynamics of uracil by two-colour photofragment Doppler spectroscopy and by two-colour slice imaging at excitation wavelengths between 268 and 235 nm. We observe the loss of a hydrogen atom upon excitation into the pipi* state.
Christof Schon+4 more
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We investigate the photochemistry and photodissociation dynamics of uracil by two-colour photofragment Doppler spectroscopy and by two-colour slice imaging at excitation wavelengths between 268 and 235 nm. We observe the loss of a hydrogen atom upon excitation into the pipi* state.
Christof Schon+4 more
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Physical Chemistry Chemical Physics, 2006
We discuss the photochemistry and photodissociation dynamics of thymine as revealed by two-colour photofragment Doppler spectroscopy and by one-colour slice imaging. Thymine is optically excited into the pipi* state, known to deactivate quickly.
Michael Schneider+5 more
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We discuss the photochemistry and photodissociation dynamics of thymine as revealed by two-colour photofragment Doppler spectroscopy and by one-colour slice imaging. Thymine is optically excited into the pipi* state, known to deactivate quickly.
Michael Schneider+5 more
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Photodissociation Dynamics of Fluorobenzene
Journal of the American Chemical Society, 2003Photodissociation of both fluorobenzene and d(5)-fluorobenzene at 193 nm under collision-free conditions has been studied in separate experiments using multimass ion imaging techniques. HF and DF eliminations were found to be the major dissociation channels.
Huang, C.L.+4 more
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Photodissociation Dynamics of Phenol [PDF]
The photodissociation of phenol at 193 and 248 nm was studied using multimass ion-imaging techniques and step-scan time-resolved Fourier-transform spectroscopy. The major dissociation channels at 193 nm include cleavage of the OH bond, elimination of CO, and elimination of H(2)O. Only the former two channels are observed at 248 nm.
Yuan-Pern Lee+7 more
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Photodissociation of bromochlorobenzenes
Journal of Photochemistry and Photobiology A: Chemistry, 2008The photodissociation kinetics of 2-, 3- and 4-bromochlorobenzene (BrClPh) and bromo-3,5-dichlorobenzene (Br-diClPh) have been studied in a molecular beam following excitation at 270 nm using femtosecond pump-probe spectroscopy. The kinetics and the dissociation dynamics in the BrClPhs were found to resemble the BrFPhs much more than the BrBrPhs. In 2-
Daniel Karlsson, Jan Davidsson
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