Synthesis of Molecular Wires by a Novel Divergent/Convergent Approach

Abstract

Described is the synthesis of oligo(2-ethylphenyl-ethynylene)s and oligo(2-(3'ethylheptyl)phenyl-ethynylene)s via an iterative divergent convergent approach. Synthesized were the monomer, dimer, tetramer, and octamer of the ethyl derivative and the monomer, dimer, tetramer, octamer, and 16-mer of the ethylheptyl derivative. The 16-mer is 128 A long. At each stage in the iteration, the length of the framework doubles. Only three sets of reaction conditions are needed for the entire iterative synthetic sequence; an iodination, a protodesilation, and a Pd/Cu-catalyzed cross coupling. The oligomers were characterized spectroscopically and by mass spectrometry.

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Document Details

Document Type
Technical Report
Publication Date
Nov 22, 1993
Accession Number
ADA273332

Entities

People

  • James Tour
  • Jeffry S. Schumm

Organizations

  • University of South Carolina

Tags

Communities of Interest

  • Advanced Electronics

DTIC Thesaurus Topics

  • Abstracts
  • Alkynes
  • Anhydrides
  • Chemical Synthesis
  • Chemistry
  • Couplings
  • Governments
  • Mass Spectrometry
  • Materials
  • Molecular Wires
  • Oligomers
  • Organic Chemistry
  • Sequences
  • South Carolina
  • Tetramers
  • United States
  • United States Government

Fields of Study

  • Chemistry

Readers

  • Operations Research
  • Polymer Science and Technology