Mihara Nozomi, Shimamura Tomonari, Takayama Ryo, Shiga Takuya, Nihei Masayuki
Department of Chemistry, Faculty of Pure and Applied Sciences, University of Tsukuba, Tennodai1-1-1, 305-8577, Tsukuba, Ibaraki, Japan.
Chemistry. 2023 Aug 15;29(46):e202300954. doi: 10.1002/chem.202300954. Epub 2023 Jun 27.
Combining metal complexes with amphiphilic molecules leads to a wide variety of functional self-assembled nanostructures. Metal complexes exhibiting spin transitions can be good candidates as the trigger to cause structural conversion of such assembly because they respond to various external stimuli. In this work, we studied a structural conversion of a supramolecular assembly containing a [Co Fe ] complex through a thermally induced electron transfer-coupled spin transition (ETCST). With an amphiphilic anion, the [Co Fe ] complex formed reverse vesicles in solution and showed thermal ETCST. In contrast, thermal ETCST in the presence of a bridging hydrogen-bond donor caused structural conversion from the reverse vesicle structure to entangled one-dimensional chains through hydrogen bond formation.
将金属配合物与两亲分子相结合可产生各种各样的功能性自组装纳米结构。表现出自旋转变的金属配合物有望成为引发此类组装体结构转变的良好触发器,因为它们能对各种外部刺激做出响应。在这项工作中,我们通过热诱导电子转移耦合自旋转变(ETCST)研究了一种含[Co Fe]配合物的超分子组装体的结构转变。在两亲性阴离子存在下,[Co Fe]配合物在溶液中形成反向囊泡,并表现出热ETCST。相比之下,在存在桥连氢键供体的情况下,热ETCST会通过氢键形成导致结构从反向囊泡结构转变为缠结的一维链结构。