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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Dynamic urea bond mediated polymerization as a synthetic route for telechelic low molar mass dispersity polyurethanes and its block copolymers

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Author(s):
Fonseca, Lucas Polo [1] ; Felisberti, Maria I. [1]
Total Authors: 2
Affiliation:
[1] Univ Estadual Campinas, Inst Chem, R Josue de Castro, POB 6154, BR-13084971 Campinas, SP - Brazil
Total Affiliations: 1
Document type: Journal article
Source: EUROPEAN POLYMER JOURNAL; v. 118, p. 213-221, SEP 2019.
Web of Science Citations: 0
Abstract

Polyurethanes (PU) constitute one of the most versatile class of polymers with respect to composition, properties and applications. However, there are a lack of synthetic strategies capable of producing PU with controlled architecture, chain end functionality, molar mass and low molar mass dispersity (D); these characteristics could considerably improve the use of PU in advanced applications. In this study, we report a method for synthesizing polyurethanes based on the dissociation equilibrium of hindered urea groups. Diisopropylamine reacts promptly with isocyanates, forming hindered ureas in a dynamic fashion and establishing a dissociation equilibrium shifted towards hindered urea formation. The equilibrium reduces the concentration of isocyanates susceptible to the polyaddition with diols and, therefore, the step growth polymerization follows a controlled pathway resulting in PU with D < 1.3 and a weight average molar mass up to 5 kDa for bulk polymerization. Moreover, urea chain end functionality is maintained after purification and telechelic PU can be obtained for further use, such as the synthesis of block copolymers capable of self-assembly. (AU)

FAPESP's process: 15/25406-5 - Organizing matter: colloids formed by association of surfactants, polymers and nanoparticles
Grantee:Watson Loh
Support Opportunities: Research Projects - Thematic Grants