THE TRIPLET STATE.

Abstract

The first order decay of triplet states of naphthalene, anthracene, phenanthrene and their halogenated derivatives was studied in cyclo-hexane and viscous paraffin solutions. The decay results partly from a bimolecular quenching process and partly from a true first order radiationless conversion to the ground state. The rate of the quenching process is a function of the solvent and, in anthracene derivatives, of the extent to which the solutions have been irradiated. The rates of radiationless conversion can only be measured when they exceed the rates of quenching processes. Bromination of anthracene is 10 times more effective in enhancing conversion than chlorination at the same position and halogenation at the 9, 10 positions has four times the effect of halogenation at other positions. (Author)

Document Details

Document Type
Technical Report
Publication Date
Mar 30, 1962
Accession Number
AD0281776

Entities

People

  • George Porter

Organizations

  • University of Sheffield

Tags

Communities of Interest

  • Materials and Manufacturing Processes

DTIC Thesaurus Topics

  • Alkanes
  • Aromatic Polycyclic Hydrocarbons
  • Bromination
  • Chemical Compounds
  • Chemical Reactions
  • Chlorination
  • Conversion
  • Cyclic Compounds
  • Ground State
  • Halogenation
  • Hydrocarbons
  • Naphthalenes
  • Organic Compounds
  • Phenanthrenes
  • Quenching

Fields of Study

  • Chemistry

Readers

  • Materials Science and Engineering.
  • Organic Chemistry