Bimane Derivatives as Fluorescent Probes for Biological Macromolecules.

Abstract

Syn-9, 10-Dixoabimanes (1,5-diazabicyclo3.3.0octa-3,6-diene-2,8-diones) are photostable, highly fluorescent compounds which can be attached to biological macromolecules as fluorescent labels. Syntheses of the important new intermediates for labeling agents, syn-tricyclic bimanes, RuCn (R=CH3 or C1) and n= 0.1,2,3 have been developed. The conversion of the compounds with n=2 into a diene has been accomplished, successfully raising the adsorption coefficient. However, interesting and surprising physical behavior conspired to drastically diminish the fluorescence quantum yield. The discovery of several routes to unsymmetrically substituted bimanes prepared by nucleophilic displacement on bromoalkyl derivatives has revealed new classes of labeling agents for macromolecules. These include a cross-linking agent.

Document Details

Document Type
Technical Report
Publication Date
Apr 18, 1987
Accession Number
ADA184048

Entities

People

  • Edward M. Kosower

Organizations

  • Tel Aviv University

Tags

DTIC Thesaurus Topics

  • Adsorption
  • Coefficients
  • Conversion
  • Displacement
  • Fluorescence
  • Macromolecules
  • Quantum Yields

Fields of Study

  • Chemistry

Readers

  • Chemistry (specifically Chemical Fluorescence)
  • Organic Chemistry

Technology Areas

  • Quantum Computing