Wu Yi-Ting, Deng Hao-Tian, Zhang Li-Yi, Li Meng-Die, Dai Feng-Rong, Chen Zhong-Ning
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
Molecules. 2025 May 5;30(9):2054. doi: 10.3390/molecules30092054.
This study is dedicated to the design of multiple redox-active oligonuclear manganese complexes supported with a bis(tetradentate) ligand (TPDP = 1,3-bis(bis(2-pyridinylmethyl)amino)-2-propanol) for high-contrast electrochromism based on the reversible redox process between Mn(II) (colorless) and Mn(III) (dark brown). Pentanuclear Mn complex (colorless) was synthesized via a one-pot reaction of Mn and TPDP, while tetranuclear Mn complex (brown) was obtained through aerial oxidation of complex . Mn complex features a central MnCl unit connected to two Mn(-TPDP) fragments through -Cl and -Cl, whereas Mn complex adopts a symmetric tetranuclear structure with two mixed-valence Mn(-TPDP)(-Cl) fragments that are further linked by -oxo. Electrochemical studies revealed multi-step reversible redox properties for both complexes, attributed to Mn/Mn processes with significant electronic coupling (Δ = 0.27-0.37 V) between Mn centers. Spectroelectrochemical analysis revealed dynamic optical modulation through the tunable d-d transition and ligand-to-metal charge transfer (LMCT) state through reversible multiple redox processes based on Mn(II) ⇆ Mn(III) interconversion. The fabricated electrochromic device (ECD) exhibited reversible and high optical contrast between the colored state (dark brown) and the bleaching state (colorless). The results highlight the potential of polynuclear manganese complexes as high-contrast electrochromic materials for next-generation smart windows and adaptive optical technologies.
本研究致力于设计多种由双(四齿)配体(TPDP = 1,3 - 双(双(2 - 吡啶基甲基)氨基)-2 - 丙醇)支撑的氧化还原活性多核锰配合物,用于基于Mn(II)(无色)和Mn(III)(深棕色)之间的可逆氧化还原过程的高对比度电致变色。通过Mn与TPDP的一锅法反应合成了五核锰配合物(无色),而四核锰配合物(棕色)则通过配合物的空气氧化获得。锰配合物具有一个中心MnCl单元,通过 -Cl和 -Cl连接到两个Mn(-TPDP)片段,而锰配合物采用对称的四核结构,具有两个混合价态的Mn(-TPDP)(-Cl)片段,它们通过 -氧代进一步连接。电化学研究表明这两种配合物都具有多步可逆氧化还原性质,这归因于Mn中心之间具有显著电子耦合(Δ = 0.27 - 0.37 V)的Mn/Mn过程。光谱电化学分析表明,基于Mn(II)⇆Mn(III)相互转化的可逆多步氧化还原过程,通过可调谐的d - d跃迁和配体到金属的电荷转移(LMCT)状态实现动态光学调制。制备的电致变色器件(ECD)在着色状态(深棕色)和漂白状态(无色)之间表现出可逆且高的光学对比度。结果突出了多核锰配合物作为下一代智能窗户和自适应光学技术的高对比度电致变色材料的潜力。