Non‐Equilibrium Assembly of Atomically‐Precise Copper Nanoclusters

Accurate structure control in dissipative assemblies (DSAs) is vital for precise biological functions. However, accuracy and functionality of artificial DSAs are far from this objective. Herein, a novel approach is introduced by harnessing complex chemical reaction networks rooted in coordination chemistry to create atomically‐precise copper nanoclusters (CuNCs), specifically Cu11(µ9‐Cl)(µ3‐Cl)3L6Cl (L = 4‐methyl‐piperazine‐1‐carbodithioate). Cu(I)–ligand ratio change and dynamic Cu(I)–Cu(I) metallophilic/coordination interactions enable the reorganization of CuNCs into metastable CuL2, finally converting into equilibrium [CuL·Y]Cl (Y = MeCN/H2O) via Cu(I) oxidation/reorganization and ligand exchange process. Upon adding ascorbic acid (AA), the system goes further dissipative cycles. It is observed that the encapsulated/bridging halide ions exert subtle influence on the optical properties of CuNCs and topological changes of polymeric networks when integrating CuNCs as crosslink sites. CuNCs duration/switch period could be controlled by varying the ions, AA concentration, O2 pressure and pH. Cu(I)‐Cu(I) metallophilic and coordination interactions provide a versatile toolbox for designing delicate life‐like materials, paving the way for DSAs with precise structures and functionalities. Furthermore, CuNCs can be employed as modular units within polymers for materials mechanics or functionalization studies. Atomically‐precise copper nanoclusters are designed for intricate non‐equilibrium assemblies to create life‐like systems. Cu(I)–ligand ratio change and dynamic Cu(I)–Cu(I) metallophilic/coordination interactions enable the reorganization into equilibrium complexes. Upon adding fuels, the system goes further cycles. Metallosupramolecules offer a new toolbox for crafting nuanced non‐equilibrium materials with tailored structures and functionalities.