The Importance of Exchange Reactions in Controlled/Living Radical Polymerization in the Presence of Alkoxyamines and Transition Metals.

Abstract

The role of exchange reactions in controlled/living radical polymerizations is analyzed. Styrene polymerization in the presence TEMPO and atom transfer radical polymerization (ATRP) catalyzed by transition metals (Cu(II)X2/2Bipy complex) are compared. ATRP proceeds approximately one order of magnitude faster than TEMPO-moderated polymerization due to a higher stationary concentration of radicals and an equilibrium more shifted to the side of radicals. ATRP can provide better defined polymers with polydispersities down to Mw/Mn approx.= l.05. This fact can he ascribed to a faster deactivation process and a smaller contribution of side reactions. The polydispersities in both systems are defined by the relative rates of the deactivation and propagation processes. The rate constant of deactivation of growing polystyryl radicals by TEMPO is in the range of kd=10(exp 8) L/mol/s, which is substantially higher than the previously reported value.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Jun 12, 1996
Accession Number
ADA309796

Entities

People

  • Krzysztof Matyjaszewski

Organizations

  • Carnegie Mellon University

Tags

Communities of Interest

  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Abstracts
  • Availability
  • Block Copolymers
  • Chemical Reaction Properties
  • Chemical Reactions
  • Chemistry
  • Copolymers
  • Exchange Reactions
  • Metals
  • Molecular Weight
  • Polymerization
  • Polymers
  • Side Reactions
  • Simulations
  • Stationary
  • Transition Metals
  • Transitions

Fields of Study

  • Chemistry

Readers

  • Organic Chemistry
  • Polymer Science and Technology