Casimiro Lorenzo, Volatron Florence, Boivin Grégoire, Abécassis Benjamin, Alves Sandra, Brouri Dalil, Montero David, Guigner Jean-Michel, Chamoreau Lise-Marie, Gontard Geoffrey, Portehault David, Li Yanling, Proust Anna, Lescouëzec Rodrigue, Ducouret Guylaine, Solé-Daura Albert, Davidson Patrick, Merland Théo, Izzet Guillaume
Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, IPCM, F-75005 Paris, France.
CNRS, ENS de Lyon, LCH, UMR 5182, 69342 Lyon Cedex 07, France.
JACS Au. 2024 Dec 5;4(12):4948-4956. doi: 10.1021/jacsau.4c00981. eCollection 2024 Dec 23.
Metallogels built in a bottom-up approach by metal coordination and supramolecular interactions have important potential for the elaboration of smart materials. In this context, we present here the formation of supramolecular coordination polymers driven by the complexation of cobalt(II) or zinc(II) ions with polyoxometalate-based hybrids displaying two terpyridine ligands in a linear arrangement. Thanks to the electrostatic interactions between the polyoxometalate cores and metal nodes, the polymer chains self-assemble into fibers that physically cross-link to form gels above a critical concentration. Using spectroscopy, microscopy, X-ray scattering, and rheometry, complemented by molecular dynamics simulations, we investigated the supramolecular organization of the chains in the fibers and the resulting processes leading to gelation. Compared to previously reported systems, these gels have improved rheological features and appealing properties, such as birefringence, luminescence, and spin crossover, paving the way for their use as building blocks for multifunctional smart materials.
通过金属配位和超分子相互作用以自下而上的方式构建的金属凝胶在制备智能材料方面具有重要潜力。在此背景下,我们在此展示了由钴(II)或锌(II)离子与基于多金属氧酸盐的杂化物络合驱动形成的超分子配位聚合物,该杂化物呈现线性排列的两个三联吡啶配体。由于多金属氧酸盐核心与金属节点之间的静电相互作用,聚合物链自组装成纤维,在临界浓度以上物理交联形成凝胶。我们使用光谱学、显微镜、X射线散射和流变学,并辅以分子动力学模拟,研究了纤维中链的超分子组织以及导致凝胶化的过程。与先前报道的体系相比,这些凝胶具有改善的流变特性和吸引人的性质,如双折射、发光和自旋交叉,为其用作多功能智能材料的构建块铺平了道路。