4.7 Article

t-Bu3P-Coordinated 2-Phenylaniline-Based Palladacycle Complex as a Precatalyst for the Suzuki Cross-Coupling Polymerization of Aryl Dibromides with Aryldiboronic Acids

Journal

ACS MACRO LETTERS
Volume 2, Issue 1, Pages 10-13

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/mz300479b

Keywords

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Funding

  1. NSF [CHE0911533]
  2. NIH [IRIS GM094709]
  3. PSC-CUNY
  4. Division Of Chemistry [0911533] Funding Source: National Science Foundation
  5. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R15GM094709] Funding Source: NIH RePORTER

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t-Bu3P-coordinated 2-phenylaniline-based palladacycle complex, [2'-(amino-kN) [1,1'-biphenyl]-2-yl-kC] chloro (trit-butylphosphine)-palladium, as a general, highly efficient precatalyst for the Suzuki cross-coupling polymerization of aryl dibromides with aryldiboronic acids is described. Such t-Bu3P-coordinated 2-aminobiphenyl-based palladacyde complex-catalyzed Suzuki cross-coupling polymerization afforded polymers within an hour, with the yields and the molecular weights comparable to or higher than that of polymers obtained by using other palladium catalysts with much longer polymerization time. Our study provided a highly efficient catalyst system for the Suzuki cross-coupling polymerization of aryl dihalides with aryldiboronic acids. Our study also paved the road for us to investigate other monodentate ligand-coordinated palladacycle complexes including N-heterocyclic carbene-coordinated ones for cross-coupling polymerizations.

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