TRIPLET STATE ZERO FIELD SPLITTINGS OF SOME STRUCTURALLY RELATED AROMATIC HYDROCARBON AND HETEROCYCLIC MOLECULES,

Abstract

The triplet state zero field splitting parameters D and E have been determined from the delta m = plus or minus 1 EPR spectra of the photo-excited triplet states of several structurally related aromatic hydrocarbons and aromatic heterocyclic molecules, using diethyl ether glasses at 77 K. The values of the splitting parameters per cm for the various molecules are as follows: biphenyl D = 0.1092, E = 0.0036; fluorene D = 0.1075, E = 0.0033; carbazole D = 0.1022, E = 0.0066; dibenzofuran D = 0.1071, E = 0.0092; dibenzothiophen D = 0.1130, E = 0.0021. The uncertainties in these numbers are plus or minus 0.2 Mk for D and plus or minus 0.1 Mk for E. Lifetimes of the triplet states were also determined. A discussion of the results in terms of conjugation of the hetero atom with the aromatic rings is given. The results are compared to the published values of D and E for phenanthrene. It is found that biphenyl is a better hydrocarbon model than phenanthrene for the heterocyclics investigated in this report. (Author)

Document Details

Document Type
Technical Report
Publication Date
Jan 01, 1966
Accession Number
AD0478238

Entities

People

  • Henry S. Judeikis
  • Seymour Siegel

Organizations

  • The Aerospace Corporation

Tags

DTIC Thesaurus Topics

  • 3-Ring Heterocyclic Compounds
  • Aromatic Compounds
  • Aromatic Hydrocarbons
  • Biphenyl
  • Chemical Compounds
  • Cyclic Compounds
  • Cyclic Hydrocarbons
  • Fluorenes
  • Hydrocarbons
  • Molecules
  • Organic Compounds
  • Phenanthrenes
  • Spectra
  • Splitting
  • Unsaturated Hydrocarbons

Fields of Study

  • Chemistry

Readers

  • Materials Science and Engineering.
  • Molecular Photonics/Laser Physics
  • Organic Chemistry