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Organocatalyzed ring-opening polymerization (ROP) of functional β-lactones: new insights into the ROP mechanism and poly(hydroxyalkanoate)s (PHAs) macromolecular structure

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Abstract

The organocatalyzed ring-opening polymerization (ROP) of various 4-alkoxymethylene-β-propiolactones (BPLORs; R = CH2CH[double bond, length as m-dash]CH2 (All), CH2Ph (Bn), (CH2)3CH3 (nBu), SiMe2tBu (TBDMS)) towards the formation of the corresponding poly(hydroxyalkanoate)s (PHAs; poly(BPLOR)s (PBPLORs)) is investigated under mild operating conditions (neat, 60 °C), simply using basic organocatalysts of the guanidine (1,5,7-triazabicyclo[4.4.0]dec-5-ene, TBD), amidine (1,8-diazabicyclo[5.4.0]-undec-7-ene, DBU) or phosphazene (2-tert-butylimino-2-diethylamino-1,3-dimethylperhydro-1,3,2diazaphosphorine, BEMP) type. The polymerization proceeds basically at the same rate as the alike organocatalyzed ROP of related β-lactones (especially the ubiquitous β-butyrolactone (BL) and alkyl β-malolactonates (MLARs)), with BEMP being significantly more active than TBD and DBU. Insights into the polymerization mechanisms are gained through detailed 1D/2D NMR spectroscopy and MALDI-ToF mass spectrometry analyses of the resulting PBPLORs and in particular through the identification of the nature of the end-capping groups. Each of the three organobases promotes the polymerization in its own way, as dictated by either its basic, nucleophilic or dual behavior.

Graphical abstract: Organocatalyzed ring-opening polymerization (ROP) of functional β-lactones: new insights into the ROP mechanism and poly(hydroxyalkanoate)s (PHAs) macromolecular structure

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Article information


Submitted
24 Jan 2020
Accepted
10 Mar 2020
First published
11 Mar 2020

Polym. Chem., 2020, Advance Article
Article type
Paper

Organocatalyzed ring-opening polymerization (ROP) of functional β-lactones: new insights into the ROP mechanism and poly(hydroxyalkanoate)s (PHAs) macromolecular structure

R. M. Shakaroun, P. Jéhan, A. Alaaeddine, J. Carpentier and S. M. Guillaume, Polym. Chem., 2020, Advance Article , DOI: 10.1039/D0PY00125B

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