Electron affinities and the electron-capture method for aromatic hydrocarbons

1968 ◽  
Vol 72 (10) ◽  
pp. 3677-3678 ◽  
Author(s):  
Lawrence E. Lyons ◽  
G. C. Morris ◽  
L. J. Warren
Keyword(s):  
Electron Capture ◽  
Aromatic Hydrocarbons ◽  
Electron Affinities ◽  
Capture Method

Electron capture by some molecules of biological significance and the determination of absolute electron affinities

1968 ◽  
Vol 21 (12) ◽  
pp. 2853 ◽  
Author(s):  
A Fulton ◽  
LE Lyons ◽  
GC Morris
Keyword(s):  
Electron Capture ◽  
Protoporphyrin Ix ◽  
Biological Significance ◽  
Molecular Orbitals ◽  
Electron Affinities ◽  
Metal Free ◽  
Capture Method

The electron capture method was applied to protoporphyrin IX and meso- porphyrin IX dimethyl esters, metal-free phthalocyanine, chlorophyll, riboflavine, nicotinamide, tetracene, and pentacene. The energy quantities obtained correlated with calculated energies of the lowest empty molecular orbitals of these molecules.

Potential Method for the Determination of Electron Affinities of Molecules: Application to Some Aromatic Hydrocarbons

1962 ◽  
Vol 84 (22) ◽  
pp. 4263-4266 ◽  
Author(s):  
W. E. Wentworth ◽  
Ralph S. Becker
Keyword(s):  
Aromatic Hydrocarbons ◽  
Potential Method ◽  
Electron Affinities

Gas phase adiabatic electron affinities of cyclopenta-fused polycyclic aromatic hydrocarbons

2008 ◽  
Vol 454 (1-3) ◽  
pp. 30-35 ◽  
Author(s):  
Petar D. Todorov ◽  
Carola Koper ◽  
Joop H. van Lenthe ◽  
Leonardus W. Jenneskens
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Gas Phase ◽  
Aromatic Hydrocarbons ◽  
Electron Affinities ◽  
Polycyclic Aromatic

New schemes for the electron-capture sensitization of aromatic hydrocarbons

1984 ◽  
Vol 302 ◽  
pp. 243-256 ◽  
Author(s):  
E.P. Grimsrud ◽  
C.A. Valkenburg
Keyword(s):  
Electron Capture ◽  
Aromatic Hydrocarbons

Electron Affinities and Ionization Potentials of Aromatic Hydrocarbons

1963 ◽  
Vol 85 (15) ◽  
pp. 2210-2214 ◽  
Author(s):  
Ralph S. Becker ◽  
W. E. Wentworth
Keyword(s):  
Aromatic Hydrocarbons ◽  
Ionization Potentials ◽  
Electron Affinities

Chemistry of radical ions: the absolute rate constant of dimerization of radical anions of 1 ,1-diphenyl ethylene

1965 ◽  
Vol 288 (1413) ◽  
pp. 212-223 ◽  
Keyword(s):  
Electron Transfer ◽  
Rate Constant ◽  
Transfer Process ◽  
Aromatic Hydrocarbons ◽  
Radical Anions ◽  
Electron Affinities ◽  
Absolute Rate ◽  
Radical Ions ◽  
Electron Transfer Process ◽  
Absolute Rate Constant

The combination of the labile radical ions, (Ph 2 C:CH 2 )7~, Na+, into dimeric dianions Na + , C - (Ph) 2 .CH 2 .CH 2 .C(Ph) - 2, Na+ was investigated by a flow and a stopflow technique. The bimolecular rate constant of combination was found to be 2 to 3 x 106 1. mole-1 s-1. The reaction was initiated by an electron transfer naphthalene^ + (P/*,2C:CH2) naphthalene+ (P/*,2C:CH^) or terphenylener + (P7fc2C:CH2) ⇔ terphenylene + (Pfe2C:CH^). The equilibrium constant of the first electron transfer process was found to be 20 and of the second about 16. These results are consistent with recent determinations of electron affinities of aromatic hydrocarbons.

Electron Affinities of Polycyclic Aromatic Hydrocarbons by Means of B3LYP/6-31+G* Calculations

2006 ◽  
Vol 110 (20) ◽  
pp. 6482-6486 ◽  
Author(s):  
Alberto Modelli ◽  
Laura Mussoni ◽  
Daniele Fabbri
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Electron Affinities ◽  
Polycyclic Aromatic

Extension of Electron Affinities and Ionization Potentials of Aromatic Hydrocarbons

1966 ◽  
Vol 45 (7) ◽  
pp. 2403-2410 ◽  
Author(s):  
Ralph S. Becker ◽  
Edward Chen
Keyword(s):  
Aromatic Hydrocarbons ◽  
Ionization Potentials ◽  
Electron Affinities
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