The arrangement of monomers and morphology of fluorinated copolymers of methyl methacrylate (MMA) were found to be important for controlling the surface energy of the materials when formed into thin films. Novel copolymers of MMA and 2,2,3,3,4,4, were prepared with different monomer placement, namely statistical and block arrangements of the monomer units. The surface energies decreased with increasing incorporation of F3MA, in a manner consistent with previous reports for similar copolymers; however, the surface energies of the block copolymers were consistently lower than the statistical copolymers. This was interpreted as arising from conformational restriction of presentation of the fluoromonomers to the surface in the statistical copolymers, and formation of phase-separated domains at the surface of the block copolymers. The morphology of the block copolymers was confirmed by small angle Xray scattering measurements, which allowed calculation of a solubility parameter for the fluorinated segments. The results have implications for the design of more environmentally acceptable materials with ultra-low surface energies. V C 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015, 53, 2633-2641 KEYWORDS: block copolymers; fluoropolymers; low surface energy; phase separation; reversible addition fragmentation chain transfer; small angle X-ray scattering INTRODUCTION The tendency for a liquid to spread and wet a surface of a polymeric substrate is determined by the balance of forces of adhesion between the liquid and the substrate, and the forces of cohesion driving the liquid into a form with a minimum surface energy, that is, a sphere. Spreading continues until the adhesion forces are matched by the combined surface forces. As we know, the forces of adhesion are determined by the magnitude of the noncovalent or van der Waal's interactions in the system. For a polar liquid such as water these are dominated by the presence of permanent dipoles, and so spreading of water is facilitated by the presence of functionalities with similar polarity within the substrate. Such polar substrates have high surface energies, as a result of the disruption of these strong forces at the material-air interface. On the contrary, it has been known for many years that the incorporation of fluorinated segments into polymers imparts low surface energy, and thus water tends to dewet extensively on planar fluorinated surfaces. These properties have led to many