34470-17-2

Basic information

• Product Name: 3-fluoronitrobenzene radical anion
• CAS NO: 34470-17-2
• Molecular Weight: 141.102
• Mol File: 34470-17-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-fluoronitrobenzene radical anion(CAS DataBase Reference)
• NIST Chemistry Reference: 3-fluoronitrobenzene radical anion(34470-17-2)
• EPA Substance Registry System: 3-fluoronitrobenzene radical anion(34470-17-2)

Safety Data

• Hazardous Substances Data: 34470-17-2(Hazardous Substances Data)

Upstream product

• 402-67-5 3-fluoro-1-nitrobenzene 
• 623-26-7 1,4-dicyanobenzene anion radical 
• 98-95-3 nitrobenzene radical anion 

Downstream Products

• 402-67-5 3-fluoro-1-nitrobenzene 
• 34473-09-1 4-Chloronitrobenzene radical anion 
• 98-95-3 nitrobenzene 
• 34467-54-4 3-Chloronitrobenzene radical anion 
• 139584-10-4 C₆H₄FNO₂*Br^(1-) 

Relevant articles and documents

Resonance Electron Capture Rate Constants for Substituted Nitrobenzenes

We report here a new method for the determination of electron capture (EC) rate constants that utilizes a pulsed electron beam mass spectrometer.The method is first tested by measurements of the known dissociative electron capture rate constants for several halogenated methanes that have been extensively studied by other techniques.The resonance electron capture (REC) rate constants of nitrobenzene (NB) and 23 substituted nitrobenzenes (SNB's) are then determined for the first time at 125 deg C in 10 Torr of methane buffer gas.The SNB's studied here include several sets of closely related structural isomers whose electron affinities (EA's) have been previously determined.It is shown that the REC rate constants of these compounds bear little systematic relationship with the EA's of these compounds.The REC rate constants of the SNB's are also compared with other previously reported characteristics associated with the negative ionization of these compounds, including their entropies of negative ionization, the lifetimes against autodetachment of their initially formed molecular anions, and the rates of autodetachment from electronically excited states of their molecular anions.

Electron Affinities of Di- and Tetracyanoethylene and Cyanobenzenes Based on Measurements of Gas-Phase Electron-Transfer Equilibria

The electron affinities of tetracyanoethylene, trans-1,2-dicyanoethylene, and eleven substituted benzonitriles as well as two naphthonitriles were determined by measurement of the electron-transfer equilibria A-+B=A+B- with a pulsed electron high ion source pressure mass spectrometer.Rate constants for exothermic electron transfer involving the cyano compounds were found to be near unit collision efficiency.The EA (tetracyanoethylene)=3.17 eV obtained in the present work is considerably higher than the 2.3 eV photodetachment value of Palmer and Lyons.The electron affinities of benzene and benzonitrile substituted by CN, CHO, and NO2 increase in the given order, while the order for nitrobenzene is CHO, CN, NO2.This reversal of order is explained on the basis of a larger attenuation of the ?-withdrawing effect relative to the field effect of substituents when the electron density in the ?* single-electron orbital is decreased.