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Issue 3, 2014
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Control over molar mass, dispersity, end-groups and kinetics in cyclopolymerization of ortho-phthalaldehyde: adapted choice of a phosphazene organocatalyst

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Abstract

The use of different phosphazene bases as catalysts has been investigated in the polymerization of ortho-phthalaldehyde (PA) in the presence of an alcohol used as the initiator. Among the catalysts considered (P1-t-Bu, P2-t-Bu and P4-t-Bu) only the less active one (P1-t-Bu) allows a very good control of the PA polymerization in terms of mass parameters (Mn, Mw and molar mass dispersity) and end-group fidelity. To confirm the structure and the mass range of the newly synthesized PPA, mass spectrometry and gel permeation chromatography have been selected as main characterization techniques. By comparison with the state-of-the-art, the kinetics of polymerization has also been significantly improved by reducing the polymerization time from several hours to a few minutes. The judicious choice of catalyst also allowed expanding the macromolecular engineering by preparing in a one-step procedure a defined and controlled polyphthalaldehyde-block-polyethylene oxide amphiphilic diblock copolymer.

Graphical abstract: Control over molar mass, dispersity, end-groups and kinetics in cyclopolymerization of ortho-phthalaldehyde: adapted choice of a phosphazene organocatalyst

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Publication details

The article was received on 19 Sep 2013, accepted on 31 Oct 2013 and first published on 01 Nov 2013


Article type: Communication
DOI: 10.1039/C3PY01307C
Citation: Polym. Chem., 2014,5, 706-711

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    Control over molar mass, dispersity, end-groups and kinetics in cyclopolymerization of ortho-phthalaldehyde: adapted choice of a phosphazene organocatalyst

    J. De Winter, A. P. Dove, A. Knoll, P. Gerbaux, Ph. Dubois and O. Coulembier, Polym. Chem., 2014, 5, 706
    DOI: 10.1039/C3PY01307C

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