Photo-assisted intersystem crossing: The predominant triplet formation mechanism in some isolated polycyclic aromatic molecules excited with pulsed lasers
Journal Article
·
· Journal of Chemical Physics
- Department of Chemistry, Stony Brook University, Stony Brook, New York 11794-3400 (United States)
Naphthalene, anthracene, and phenanthrene are shown to have very long-lived triplet lifetimes when the isolated molecules are excited with nanosecond pulsed lasers resonant with the lowest singlet state. For naphthalene, triplet state populations are created only during the laser pulse, excluding the possibility of normal intersystem crossing at the one photon level, and all molecules have triplet lifetimes greater than hundreds of microseconds, similar to the behavior previously reported for phenylacetylene. Although containing 7–12 thousand cm{sup −1} of vibrational energy, the triplet molecules have ionization thresholds appropriate to vibrationless T{sub 1} states. The laser power dependences (slopes of log-log power plots) of the excited singlet and triplet populations are about 0.7 for naphthalene and about 0.5 for anthracene. Kinetic modeling of the power dependences successfully reproduces the experimental results and suggests that the triplet formation mechanism involves an enhanced spin orbit coupling caused by sigma character in states at the 2-photon level. Symmetry adapted cluster-configuration interaction calculations produced excited state absorption spectra to provide guidance for estimating kinetic rates and the sigma character present in higher electronic states. It is concluded that higher excited state populations are significant when larger molecules are excited with pulsed lasers and need to be taken into account whenever discussing the molecular photodynamics.
- OSTI ID:
- 22493457
- Journal Information:
- Journal of Chemical Physics, Journal Name: Journal of Chemical Physics Journal Issue: 4 Vol. 143; ISSN JCPSA6; ISSN 0021-9606
- Country of Publication:
- United States
- Language:
- English
Vibrationally assisted below-threshold ionization
|
journal | June 2017 |
Similar Records
Photo-assisted intersystem crossing: The predominant triplet formation mechanism in some isolated polycyclic aromatic molecules excited with pulsed lasers
Intersystem Crossing Mechanisms and Single Molecule Fluorescence: Terrylene in Anthracene Crystals
Configuration Mixing Upon Reorganization of Dihedral Angle Induces Rapid Intersystem Crossing in Organic Photoredox catalyst
Journal Article
·
Mon Jul 27 20:00:00 EDT 2015
· Journal of Chemical Physics
·
OSTI ID:1213379
Intersystem Crossing Mechanisms and Single Molecule Fluorescence: Terrylene in Anthracene Crystals
Journal Article
·
Sun May 15 00:00:00 EDT 2005
· Optics and Spectroscopy
·
OSTI ID:20722868
Configuration Mixing Upon Reorganization of Dihedral Angle Induces Rapid Intersystem Crossing in Organic Photoredox catalyst
Journal Article
·
Mon May 25 20:00:00 EDT 2020
· Physical Chemistry Chemical Physics. PCCP
·
OSTI ID:1630695