Article ID Journal Published Year Pages File Type
1314146 Journal of Fluorine Chemistry 2011 7 Pages PDF
Abstract

We obtained, through an original multi step synthetic approach with 60–80% selectivity, a novel family of hydrofluoropolyethers (HFPEs) characterized by a macromeric perfluoropolyether (PFPE) body end-capped, on one or both sides, by a 1,1-difluoroethoxy group. We synthesized these HFPEs trough an apparently conventional hydrogenation of PFPE precursors end-capped by reducible acyl halide groups and subsequent Cl cleavage by hydrogen, promoted by UV light in presence of hydrogen radical donor or by a metal catalytic system in presence of H2. The physico-chemical properties of these HFPEs were described and compared to those of similar perfluorinated or partially hydrogenated molecules, obtaining master curves of general validity when temperature dependent properties, like viscosity, were compared under temperature reduced condition. The contribution of the end-groups to the specific property, vanishing at a sufficient high molecular weight, was demonstrated more and more important at the lowest oligomerization degrees.

Graphical abstractA novel family of hydrofluoropolyethers (HFPEs) has been obtained through an original synthetic approach. The physico-chemical properties of these HFPEs are here described and compared to those of similar perfluorinated or partially hydrogenated molecules. The contribution of the end-groups to the specific property vanishes at a sufficient high molecular weight, but becomes more and more important at the lowest oligomerization degrees.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Synthesis of a new family of hydrofluoropolyethers (HFPEs). ► Analysis of their main physico-chemical properties. ► Comparison with analogous fluoropolyethers and perfluorinated series. ► Understanding the interplay of perfluorinated backbone and chain ends.

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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