“…Theoretically, coupling strong electron-donating groups with strong acceptor groups can ensure efficient NIR-II emission . BODIPY, rhodamine, and cyanine-based D-A NIR-II dyes with good photophysical properties have been developed, showing great potential as NIR-II imaging agents. − However, they always suffer from the problem of poor hydrophilicity, photostability, and fast elimination. , Based on the classical D-A-D dye structure, D-A polymers were also developed with a more significant Stokes shift and better extinction coefficient, but the enormous molecular weight, hard to control degree of polymerization, and the potential long-term retention toxicity limit their clinical transportation. − D-A NIR-II small molecular dyes that reduce one donor group from the D-A-D skeleton have a more simplified structure with a more significant Stokes shift, better photostability, and easier metabolism ability. However, few of these D-A dyes have been reported so far.…”