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Designing artificial systems to mimic chiral superstructures and exploring how achiral molecules precisely modulate their chirality is crucial to understand the origin of homochirality in nature. Herein, the tunability nature of supramolecular chirality is subtly applied to fabricate robust chiral covalent polymers with controlled macroscopic helicity. When using conventional supramolecular transcription methods to prepare chiral poly(m‐phenylenediamine), simply introducing various small amounts of achiral diaminopyridines (DAPs) to copolymerize with m‐phenylenediamine (MPD) enables the resulting chiral copolymers with adjustable helical configurations and chiroptical activities in an enantiopure template system. The strong hydrogen bonds between DAPs and the template molecules ((S)/(R)‐PhgC16) proved to be the driving force for guiding the chiral polymerization mode of MPD. Impressively, the exquisite self‐sorting phenomenon is observed by tuning the stoichiometric ratio of DAP and (R)‐PhgC16, where the as‐prepared copolymers with opposite helicity can exist simultaneously to form a double network structure and their chiroptical activity can be well regulated. In addition, based on such a copolymerization strategy, a conceptual library of helical functional copolymers is built with editable polymer types including conducting polymers and designable amine‐aldehyde condensation‐based polymers. This copolymerization‐mediated synthetic strategy may facilitate the development of chiral polymers with controlled morphologies and dynamic compositions. [ABSTRACT FROM AUTHOR]

A novel molecular imprinted polymer (MIP) based thermo-sensitive electrochemical sensor was fabricated by an electropolymerization method using N-isopropylacryamide and theophylline as the monomer and the template molecule, respectively. The [Fe(CN)6]3−/[Fe(CN)6]4−was used as an electrochemical probe to investigate the electrochemical behavior of the prepared sensor. The influence factors including electropolymerization cycles, the utilization of cross-linkers, and the extraction solution were investigated in detail. The sensor exhibited excellent thermo-sensitive behavior to environmental temperature stimuli and displayed a good recognition capacity for template molecules from its analogues. This approach may allow the application of this type of intelligent electrochemical sensor for stimulus-responsive recognition of template molecules. [ABSTRACT FROM AUTHOR]