Diarylethene Self-Assembled Monolayers: Cocrystallization and Mixing-Induced Cooperativity Highlighted by Scanning Tunneling Microscopy at the Liquid/Solid Interface
International audienceThe control over 2-D multi-component molecular orderings on surfaces is a key technology to realize advanced materials with stimuli-responsive properties. The fractional coverage (θ) at a given concentration can be determined from two parameters: the equilibrium constant (Ke) and the degree of cooperativity (σ). The parameters for the formation of self-assembled monolayer of pure diarylethene isomers were obtained by STM measurements on HOPG. These mono-component parameters were used as references to highlight a cocrystallization process between the open-and closed-ring isomers. Moreover it was observed that the presence of the closed-ring isomer induces cooperativity in the formation of the molecular ordering of the open-ring isomer. The quantitative analysis of the ordering formation process by using a model simulation presented in this work provides a better understanding of mixing of components in a molecular ordering and photoinduced interchanges at the liquid/solid interface. (1) Sakano, T.; Imaizumi, Y.; Hirose, T.; Matsuda, K. Chem. Lett. 2013, 42, 1537. (2) Yokoyama, S.; Hirose, T.; Matsuda, K. Chem. Commun. 2014, 50, 5964. (3) Frath, D.; Sakano, T.; Imaizumi, Y.; Yokoyama, S.; Hirose, T.; Matsuda, K. Chem. Eur. J. 2015, 21, 11350
