A new oligo(hexafluoropropylene oxide)-b-oligo(ethylene oxide) diblock surfactant obtained by radical reactions. Issue 1 (25th September 2014)

• Record Type: Journal Article
• Authors: Lapčík, Jiří; Gimello, Olinda; Ladmiral, Vincent; Friesen, Chadron Mark; Ameduri, Bruno
• Is Part Of: Polymer chemistry. Volume 6:Issue 1(2015)
• Page Start: 79
• Page End: 96
• Publication Date: 2014-09-25
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/c4py00965g
• Languages: English
• ISSNs: 1759-9954

Abstract

Abstract : The synthesis and characterization of a new oligo(hexafluoropropylene oxide)- b -oligo(ethylene oxide), oligo(HFPO)- b -oligo(PEG), diblock co-oligomer are presented. Abstract : The synthesis and characterization of a new oligo(hexafluoropropylene oxide)- b -oligo(ethylene oxide), oligo(HFPO)- b -oligo(PEG), diblock co-oligomer are presented. First, the model reactions dealing with the radical addition of 1-iodoperfluorohexane (C6 F13 I) onto allyl alcohol and allyl-O-PEG-OCH3 were optimized in terms of the choice of the initiator (azobisisobutyronitrile [AIBN], tert -butylperoxypivalate [TBBPi], and benzoyl peroxide [BPO]) and of the solvent, temperature, and time. Allyl-O-PEG-OCH3 was obtained from the etherification of ω-hydroxy-PEG with allyl bromide. End-capping of oligo(HFPO) with PEG was successfully achieved by the radical addition of 1-iodoperfluoropropyl-2-oligo(hexafluoropropylene oxide) [oligo(HFPO)-CF(CF3 )CF2 I] onto allyl-O-PEG-OCH3 using the best conditions of the model reactions. Although TBPPi failed and led to oligo(HFPO)-isobutyl iodide, AIBN and BPO yielded oligo(HFPO)-CH2 CHICH2 -oligo(PEG). The selective reduction of the latter compound led to oligo(HFPO)- b -oligo(PEG) in 77% yield, the surface tension properties of which were compared to those of commercially available ammonium perfluorooctanoate (APFO) and perfluorooctanoic acid (PFOA). Its critical micelle concentration was 0.04 g mol −1 . All models, intermediates, and diblock co-oligomers were characterized by 1 H, 19 F, and 13 C NMR spectroscopy as well as matrix assisted laser desorption ionization (MALDI) and atmospheric pressure solids analysis probe (ASAP) time-of-flight mass spectrometry (TOF-MS).