Smart molecular design of NIR-II organic fluorophores through self-driven iterative evolution, deep learning, and fragment-based assembly.

Authors

Yu Zhang, Zhubin Hu, Xinyuan Wang, Zhenrong Sun, Yongye Liang, Cheng Zhong, Haitao Sun

Published in

Smart molecules : open access. Pages e70064. Jun 10, 2026. Epub Jun 10, 2026.

Abstract

Near-infrared II (NIR-II, 1000-1700 nm) emissive molecules are highly valued for biomedical imaging, phototherapy, and optoelectronic applications due to their deep tissue penetration, reduced autofluorescence, and high signal-to-noise ratio. However, their rational design remains challenging, as conventional discovery relies heavily on labor-intensive synthesis, limited quantum chemical calculations, and inefficient trial-and-error exploration. To overcome these limitations, an iterative AI-driven molecular evolution strategy (AI4NIR-II 1.0) is introduced that integrates time-dependent density functional theory (TDDFT), transformer-based predictive modeling, and generative molecular design. Starting from donor-acceptor-donor (D-A-D) and donor-donor-acceptor-donor-donor (D-D-A-D-D) fragment scaffolds, a predictive model for both absorption and emission properties was trained based on a high quality dataset containing ∼16,000 molecules annotated by the optimally-tuned range-separated LC-ωHPBE* (OTRS) functional. A fine-tuned generative model was subsequently incorporated into a self-refining-loop workflow that cycles through molecular generation, property screening, and dataset augmentation. The model achieves excellent predictive performance for both emission and absorption properties, that is mean absolute errors of 19 nm for emission peak wavelengths and of 11 nm for absorption peak wavelengths, and correlation coefficient (R ²) exceeding 0.98 for wavelengths and oscillator strengths compared to OTRS-TDDFT calculations. In addition, the resulting framework efficiently identifies promising NIR-II candidates with accurate photophysical property predictions, and achieves speed improvements of three to four orders of magnitude over TDDFT calculations. Beyond accelerating NIR-II fluorophore discovery, this self-driven approach establishes a scalable and generalizable paradigm for NIR-II molecular design, with applicability extending to optoelectronic materials and therapeutic compounds.

PMID:
42500723
Bibliographic data and abstract were imported from PubMed on 25 Jul 2026.

Read full publication at:
Please sign in to see all details.

Stats

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.