TY - JOUR
T1 - Probing the Lifetimes of Internally Excited Amyl Nitrite Cations
AU - Rosenberg, Martin
AU - Sølling, Theis Ivan
AU - Z. Bisgaard, Christer
AU - M. Weber, Peter
AU - P. Minitti, Michael
AU - Rusteika, Nerijus
AU - Deb, Sanghamitra
N1 - Paper id:: 10.1021/jp102393g
PY - 2010/7/8
Y1 - 2010/7/8
N2 - The photoelectron spectrum shows that multiphoton ionization of amyl nitrite, C5H11ONO, using ultrafast laser pulses deposits up to 3.7 eV of energy into internal degrees of freedom. As a result, the molecules fragment to produce various daughter ions of masses 87, 71, 60, 57, 41, 30, 29, and 27. Absorption of an additional photon with 3 eV of energy by the ions yields transients with picosecond decay times, revealing the time scale of the decomposition dynamics of the initially prepared parent ion. Each mass peak has a distinct time constant, in the range of 1.2 to 7.9 ps, emphasizing the dependence of the fragmentation mechanism on the ion internal energy.
AB - The photoelectron spectrum shows that multiphoton ionization of amyl nitrite, C5H11ONO, using ultrafast laser pulses deposits up to 3.7 eV of energy into internal degrees of freedom. As a result, the molecules fragment to produce various daughter ions of masses 87, 71, 60, 57, 41, 30, 29, and 27. Absorption of an additional photon with 3 eV of energy by the ions yields transients with picosecond decay times, revealing the time scale of the decomposition dynamics of the initially prepared parent ion. Each mass peak has a distinct time constant, in the range of 1.2 to 7.9 ps, emphasizing the dependence of the fragmentation mechanism on the ion internal energy.
U2 - 10.1021/jp102393g
DO - 10.1021/jp102393g
M3 - Journal article
C2 - 20540545
SN - 1089-5639
VL - 114
SP - 7021
JO - Journal of Physical Chemistry Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory
JF - Journal of Physical Chemistry Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory
IS - 26
ER -