Abstract
The development of graph neural networks for predicting molecular properties has garnered significant attention, as it enables the correlation of quickly computable atomic and bond descriptors with overall molecular properties. With the rising interest in photochemistry and photocatalysis as sustainable alternatives to thermal reactions, curation of virtual databases of computed photophysical properties for training of machine learning models has become popular. Unfortunately, current efforts fail to consider the exciton localization onto different chromophores of the same molecule, leading to potentially large prediction errors. Here we describe a molecular fragmentation strategy that can be used to overcome this limitation, while also providing a way to compare structural diversity between different libraries. Using a newly generated database of 46 432 adiabatic S(0)-T(1) energy gaps (ALFAST-DB), we compare its diversity with two datasets from the literature and demonstrate that a fragment-based delta learning approach improves model generalizability while achieving accuracies comparable to those of traditional message passing graph neural network architectures (MPGNN).