Results 161 to 170 of about 36,044 (198)

Photodissociation and electron-collision induced dissociation of C₅H₂F₁₀ using photoelectron-photoion coincidence spectroscopy and quantum chemistry. [PDF]

Sci Rep
Tran NT, Hayashi T, Iwayama H, Ishikawa K.   +3 more
europepmc   +1 more source

Insights into the piezo-photocatalytic activity and optimized magnetic recovery of hybrid bismuth ferrite-based nanosystems. [PDF]

Nanoscale Adv
Maltoni P, Ghibaudo N, Kumar A, Barucca G, Vocciante M, Locardi F, Varvaro G, Slimani S, Ferretti M, Sarkar T, Reverberi A, Alberti S, Peddis D.   +12 more
europepmc   +1 more source

IR-Action Spectroscopy of the Astrochemically Relevant HCCS⁺ Cation. [PDF]

ACS Earth Space Chem
Michielan M, Steenbakkers K, Ascenzi D, Diprose JA, Polášek M, Brünken S, Romanzin C, Heazlewood BR, Puzzarini C, Richardson V.   +9 more
europepmc   +1 more source

A time-independent, variational method for studying the photodissociation of triatomic molecules.

Phys Chem Chem Phys
Pezzella M, Mitev G, Yurchenko SN, Tennyson J, Mitrushchenkov AO.   +4 more
europepmc   +1 more source

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Photodissociation of uracil

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.
Michael, Schneider, Christof, Schon, Ingo, Fischer, Luis, Rubio-Lago, Theofanis, Kitsopoulos   +4 more
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Photodissociation of thymine

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, Raman, Maksimenka, F Johannes, Buback, Theofanis, Kitsopoulos, Luis R, Lago, Ingo, Fischer   +5 more
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Photodissociation dynamics of pyridine

The Journal of Chemical Physics, 2005
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 ...
Ming-Fu, Lin, Yuri A, Dyakov, Chien-Ming, Tseng, Alexander M, Mebel, Sheng Hsien, Lin, Yuan T, Lee, Chi-Kung, Ni   +6 more
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Molecular photodissociation

The Journal of Chemical Physics, 1974
In this paper we present a quantum mechanical model for direct photodissociation and for predissociation of polyatomic molecules in terms of a sequential decay scheme involving multiple coupled continua, where each continuum corresponds to a different internal vibrational state of the fragments.
Shaul Mukamel, Joshua Jortner
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Photodissociation Dynamics of Fluorobenzene

Journal of the American Chemical Society, 2003
Photodissociation 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., Jiang, J.C., Mebel, A.M., Lee, Y.T., Ni, C.K.   +4 more
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Photodissociation of Triatomic Hydrogen

Physical Review Letters, 1988
The unstable ground-state potential surface of triatomic hydrogen has served as prototype for the development of bimolecular reaction-rate theory, and is still largely territory only of theoretical chemistry. While the ground electronic state of H/sub 3/ is dissociative, electronically excited states of this molecule are tightly bound. These states are
, Cosby, , Helm
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