Transition-metal complexes (TMCs) are promising photosensitizers for Type~I photodynamic therapy (PDT), where electron-transfer processes can generate reactive oxygen species under hypoxic conditions. Yet identifying candidates with the required ground- and excited-state redox energetics remains challenging across the vast chemical space of TMCs. Here, we develop a data-efficient active learning (AL) framework for the discovery of Type~I active TMC photosensitizers by combining a chemically structured design space of over 2.1 million Ru(II), Os(II), and Ir(III) complexes with targeted DFT calculations and pretrained atomistic representations. With only 300 quantum-chemical evaluations, the approach efficiently enriches candidates within a mechanistically defined optimal redox region. Analysis of the viable complexes reveals chemical design principles linking metal identity, ligand framework, substituent pattern, and physicochemical properties to Type~I photoreactivity, including a pronounced preference for Os(II)-based complexes and electronically asymmetric ligand environments along with combination of electronic donating and accepting substituents. More broadly, the strategy presented herein provides a scalable, mechanism-guided route for the rational design of transition-metal photocatalysts for applications spanning biomedicine, solar energy conversion, and photoredox chemistry.
@article{arxiv.2603.19912,
title = {Data-Efficient Active Learning Discovery of Transition Metal Photosensitizers for Type I Photodynamic Therapy},
author = {Alessio Fallani and Pi A. B. Haase and Julianne F. F. Eckert and Luukas Nikkanen and Sherri A. McFarland and Martina Stella and Fabijan Pavošević},
journal= {arXiv preprint arXiv:2603.19912},
year = {2026}
}