| Literature DB >> 28406296 |
Emre H Discekici1,2, Athina Anastasaki2, Revital Kaminker2, Johannes Willenbacher2, Nghia P Truong3, Carolin Fleischmann2, Bernd Oschmann2, David J Lunn2,4, Javier Read de Alaniz1,2, Thomas P Davis3,5, Christopher M Bates2,6,7, Craig J Hawker1,2,6.
Abstract
A highly efficient photomediated atom transfer radical polymerization protocol is reported for semi-fluorinated acrylates and methacrylates. Use of the commercially available solvent, 2-trifluoromethyl-2-propanol, optimally balances monomer, polymer, and catalyst solubility while eliminating transesterification as a detrimental side reaction. In the presence of UV irradiation and ppm concentrations of copper(II) bromide and Me6-TREN (TREN = tris(2-aminoethyl amine)), semi-fluorinated monomers with side chains containing between three and 21 fluorine atoms readily polymerize under controlled conditions. The resulting polymers exhibit narrow molar mass distributions (Đ ≈ 1.1) and high end group fidelity, even at conversions greater than 95%. This level of control permits the in situ generation of chain-end functional homopolymers and diblock copolymers, providing facile access to semi-fluorinated macromolecules using a single methodology with unprecedented monomer scope. The results disclosed herein should create opportunities across a variety of fields that exploit fluorine-containing polymers for tailored bulk, interfacial, and solution properties.Entities:
Year: 2017 PMID: 28406296 DOI: 10.1021/jacs.7b01694
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419