Ionization Potentials of Polycyclic Aromatic Hydrocarbons

Nature ◽  
1964 ◽  
Vol 201 (4925) ◽  
pp. 1214-1215 ◽  
Author(s):  
HARUO KURODA
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Ionization Potentials ◽  
Polycyclic Aromatic

Single- and double-ionization potentials of polycyclic aromatic hydrocarbons and fullerenes by photon and electron impact

1994 ◽  
Vol 72 (11-12) ◽  
pp. 1060-1069 ◽  
Author(s):  
S. Tobita ◽  
S. Leach ◽  
H. W. Jochims ◽  
E. Rühl ◽  
E. Illenberger ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Synchrotron Radiation ◽  
Electron Impact ◽  
Aromatic Hydrocarbons ◽  
Double Ionization ◽  
Ionization Potentials ◽  
Electrostatic Model ◽  
Yield Curves ◽  
Multiple Ionization ◽  
Polycyclic Aromatic

Single- and double-ionization appearance potentials of 21 polycyclic aromatic hydrocarbons (PAHs) were determined by measurement of photoion yield curves using a synchrotron radiation source. Analogous measurements were made by electron impact on three PAHs. The origin of differences, of up to 4 eV, between appearance potentials for double ionization by photon and electron impact is discussed. The ratio of the double- to single-ionization potentials of PAHs was found to be 2.65 ± 0.06 for photon impact, significantly lower than for electron-impact and charge-stripping measurements. An electrostatic model, which considers that PAHs ionize like fragments of graphite, is applied to the PAHs studied and to data on the fullerenes C60 and C70. The validity and limitations of the model are discussed and its analytical and predictive propensities concerning multiple-ionization potentials and processes are demonstrated.

The Assessment of Contamination and Source of Polycyclic Aromatic Hydrocarbons from the Sediments of the Someş River

2019 ◽  
Vol 64 (1) ◽  
pp. 55-67
Author(s):  
Vlad Pӑnescu ◽  
◽  
Mihaela Cӑtӑlina Herghelegiu ◽  
Sorin Pop ◽  
Mircea Anton ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Polycyclic Aromatic

1,1’-Biaceanthrylene and 2,2'-Biaceanthrylene: Models for Linking Larger Polycyclic Aromatic Hydrocarbons via Five-Membered Rings

2019 ◽  
Author(s):  
Yachu Du ◽  
Kyle Plunkett
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Polycyclic Aromatic Hydrocarbon ◽  
Aromatic Hydrocarbon ◽  
Electronic Properties ◽  
Aromatic Hydrocarbons ◽  
Model Systems ◽  
Redox Potentials ◽  
Dimer Model ◽  
Optical And Electronic Properties ◽  
Polycyclic Aromatic

We show that polycyclic aromatic hydrocarbon (PAH) chromophores that are linked between two five-membered rings can access planarized structures with reduced optical gaps and redox potentials. Two aceanthrylene chromophores were connected into dimer model systems with the chromophores either projected outward (2,2’-biaceanthrylene) or inward (1,1’-biaceanthrylene) and the optical and electronic properties were compared. Only the planar 2,2’-biaceanthrylene system showed significant reductions of the optical gaps (1 eV) and redox potentials in relation to the aceanthrylene monomer.<br>

1,1’-Biaceanthrylene and 2,2'-Biaceanthrylene: Models for Linking Larger Polycyclic Aromatic Hydrocarbons via Five-Membered Rings

2019 ◽  
Author(s):  
Yachu Du ◽  
Kyle Plunkett
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Polycyclic Aromatic Hydrocarbon ◽  
Aromatic Hydrocarbon ◽  
Electronic Properties ◽  
Aromatic Hydrocarbons ◽  
Model Systems ◽  
Redox Potentials ◽  
Dimer Model ◽  
Optical And Electronic Properties ◽  
Polycyclic Aromatic

We show that polycyclic aromatic hydrocarbon (PAH) chromophores that are linked between two five-membered rings can access planarized structures with reduced optical gaps and redox potentials. Two aceanthrylene chromophores were connected into dimer model systems with the chromophores either projected outward (2,2’-biaceanthrylene) or inward (1,1’-biaceanthrylene) and the optical and electronic properties were compared. Only the planar 2,2’-biaceanthrylene system showed significant reductions of the optical gaps (1 eV) and redox potentials in relation to the aceanthrylene monomer.<br>

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