MOLECULAR COMPLEXES OF AROMATIC HYDROCARBON AND AZAHYDROCARBON ACCEPTORS.

Abstract

The strong donor properties of tetrakis (dimethylamino) ethylene (MAE) are determined by its interactions with pi acceptors. Colors of n-hexane solutions of this donor with pyrene, anthracene, and perylene are ascribed to intermolecular charge-transfer transitions, where the hydrocarbons function as electron acceptors. Azahydrocarbons similarly produce colors and are stronger acceptors. All association constants for complex formation ith the tetraaminoethylene are close t6 zero and this is ascribed to the bulk of the TMAE molecule, and all colors may be made to disappear in the frozen solutions or in the frozen, pure materials. These results and experimental evidence from other sources are correlated with a proposed electronic structure of TMAE. A consideration of the factors that stabilize acceptor-donor complexes, is used to reinterpret an earlier proposal that such an interaction occurs between the methylbenzenes and anthracene. (Author)

Document Details

Document Type
Technical Report
Publication Date
Jul 01, 1966
Accession Number
AD0485272

Entities

People

  • P. R. Hammond
  • R. H. Knipe

Organizations

  • Naval Air Weapons Station China Lake

Tags

DTIC Thesaurus Topics

  • Acyclic Hydrocarbons
  • Alkenes
  • Aromatic Hydrocarbons
  • Aromatic Polycyclic Hydrocarbons
  • Charge Transfer
  • Chemical Compounds
  • Cyclic Hydrocarbons
  • Electron Acceptors
  • Electrons
  • Ethylenes
  • Hydrocarbons
  • Materials
  • Molecules
  • Organic Compounds

Fields of Study

  • Chemistry

Readers

  • Electrochemical Surface Science
  • Materials Science and Engineering.
  • Organic Chemistry

Technology Areas

  • Microelectronics
  • Microelectronics - Graphene