Abstract
Conjugated sequence-defined polymers represent a cutting-edge area of polymer science, merging the precision of biological macromolecules with the versatility of synthetic polymers and the unique properties of conjugated systems. While early reports focused on activation/deactivation strategies, this article presents the first orthogonal approach to developing sequence-defined conjugated macromolecules (CMs), incorporating a new monomer at each reaction step. In CMs, the primary monomer sequence meticulously determines the optoelectronic properties. Step-by-step, features such as structural defects, chain length, dispersity, functional groups, topology, and monomers used in the backbone, are carefully considered and controlled, with optical data provided to support the necessity of sequence-defined approaches in CMs. Additionally, a beyond state-of-the-art and repeatable modular approach is introduced, connecting different orthogonally developed sequences. This method enhances efficiency and accelerates the synthesis process, facilitating comprehensive structure-property analyses, paving the way for tunable materials with record-breaking properties.