516 wileyonlinelibrary.com COMMUNICATION www.MaterialsViews.com www.advopticalmat.depreparation of compression sensitive inverse opals which allow the mechanical tuning of the photonic stopgap position. [ 18 ] Elastomers have also played a fundamental role for studying color tunable photonic crystals (PCs), [ 19,20 ] whose lattice parameter might be controlled by deformation (mechanochromic effect) or elastomer swelling. [ 21 ] An equivalent approach was proposed for the development of tunable phononic crystals. [ 22 ] Another active area of research concerns fl exible systems implemented, for instance, as UV-fi lters [ 23 ] and light emitting diodes or displays. [ 24 ] The present work addresses the fabrication of periodic nanofeatures with SME by using a replica molding approach for imprinting a 2D photonic nanostructure on the surface of a shape-memory elastomer. Structural and optical characterization of the as-produced system allowed to demonstrate its shape-memory functionality for confi guring the lattice parameter or erasing the nanopattern. This property might be very attractive, for example, for the development of reusable or self-healing photonic elements with adaptive properties.Polydiolcitrates (PDCs), fi rst described by Ameer and colleagues in 2004, [ 25 ] have been recently identifi ed as thermoresponsive elastomers presenting SME. [ 26 ] However, as far as we know, their applicability in the accomplishment of photonic nanostructured systems has not been reported in the literature yet. The synthesized polyester networks were obtained upon:(1) increase of the mol ratio of hydroxyl to carboxyl groups in the reaction mixture (4:3 in hydroxyl-dominant PDCs versus 1:1 in the original ones) and (2) the use of a more hydrophobic diol (e.g., 1,12-dodecanediol, DD). These polymers include covalent netpoints responsible for the permanent shape and hydrophobic micro-domains (either pre-polymer or DD-rich domains) physically cross-linked by intermolecular hydrophobic interactions as switch structures to fi x the temporary shape. To investigate the SME of these polymers for potential photonic applications, we followed the general procedure depicted in Figure 1 . The fi rst step consisted of the synthesis of the pre-polymer solution composed of DD and citric acid. 1 H nuclear magnetic resonance ( 1 H-NMR) confi rmed the mol ratio expected for both components (1.5) and the beginning of the condensation reaction (e.g., multiplicity of peaks at 2.6-2.9 ppm) (see Supporting Information (SI), Figure S7). Nanopatterning of the elastomer surface was achieved by using an approach inspired in soft-lithography [ 27 ] and, more specifi cally, in replica molding (Figure 1 a). [ 28,29 ] Briefl y, the pre-polymer solution was spread over the template, in our case a colloidal monolayer composed of polystyrene (PS) spheres of 870 nm in diameter ( d ). After curing at 90 °C for 12 h, the resulting cross-linked poly mer (PDDC-HD) was peeled off from the monolayer. When evaluating the cross-linking degree of the so-produced elast...