arXiv subjects

Shangqian Chen

Publications and source records attributed to Shangqian Chen.

3 recordsLinked to original sources

arXiv2026

3D Molecular Representation Learning for Organic Mixtures: Viscosity and Density Prediction

The viscosity and density of organic mixtures are essential properties for designing lubricants, solvents, and heat transfer fluids. In engineering practice, formulating a functional fluid requires understanding how these properties change with composition and temperature. However, exhaustive experimental characterization across the full parameter space is impractical due to the vast number of possible species and combinations. Here we introduce a mixture-aware 3D molecular representation learning strategy, built upon a pre-trained molecular encoder, that jointly encodes component structures, mole fractions, and temperature to achieve accurate predictions for organic mixtures. Fine-tuning on publicly available datasets covering a wide range of binary organic mixtures yields test-set R2 values of 0.973 for dynamic viscosity and 0.996 for density, significantly outperforming traditional machine learning baselines. Beyond this overall accuracy, the model captures non-monotonic viscosity changes upon mixing, surpassing simple linear or logarithmic mixing rules. The architecture is extendable to ternary and multicomponent mixtures, as verified via preliminary experiments. Using this model, we quantitatively analyze how molecular structure-branching, cycloalkane, and aromatic rings-affects viscosity-temperature behavior, which benefits the design of lubricants with superior viscosity-temperature performance. Altogether, this work provides a practical, data-driven tool for mixture property prediction, accelerating the rational formulation of functional fluids in chemical engineering.

physics.chem-ph↗

arXiv2025

MolParser: End-to-end Visual Recognition of Molecule Structures in the Wild

In recent decades, chemistry publications and patents have increased rapidly. A significant portion of key information is embedded in molecular structure figures, complicating large-scale literature searches and limiting the application of large language models in fields such as biology, chemistry, and pharmaceuticals. The automatic extraction of precise chemical structures is of critical importance. However, the presence of numerous Markush structures in real-world documents, along with variations in molecular image quality, drawing styles, and noise, significantly limits the performance of existing optical chemical structure recognition (OCSR) methods. We present MolParser, a novel end-to-end OCSR method that efficiently and accurately recognizes chemical structures from real-world documents, including difficult Markush structure. We use a extended SMILES encoding rule to annotate our training dataset. Under this rule, we build MolParser-7M, the largest annotated molecular image dataset to our knowledge. While utilizing a large amount of synthetic data, we employed active learning methods to incorporate substantial in-the-wild data, specifically samples cropped from real patents and scientific literature, into the training process. We trained an end-to-end molecular image captioning model, MolParser, using a curriculum learning approach. MolParser significantly outperforms classical and learning-based methods across most scenarios, with potential for broader downstream applications. The dataset is publicly available in huggingface.

cs.CV↗

arXiv2025

High-Accuracy Physical Property Prediction for Organics via Molecular Representation Learning: Bridging Data to Discovery

The ongoing energy crisis has underscored the urgent need for energy-efficient materials with high energy utilization efficiency, prompting a surge in research into organic compounds due to their environmental compatibility, cost-effective processing, and versatile modifiability. To address the high experimental costs and time-consuming nature of traditional trial-and-error methods in the discovery of highly functional organic compounds, we apply the 3D transformer-based molecular representation learning algorithm to construct a pre-trained model using 60 million semi-empirically optimized structures of small organic molecules, namely, Org-Mol, which is then fine-tuned with public experimental data to obtain prediction models for various physical properties. Despite the pre-training process relying solely on single molecular coordinates, the fine-tuned models achieves high accuracy (with $R^2$ values for the test set exceeding 0.95). These fine-tuned models are applied in a high-throughput screening process to identify novel immersion coolants among millions of automatically constructed ester molecules, resulting in the experimental validation of two promising candidates. This work not only demonstrates the potential of Org-Mol in predicting bulk properties for organic compounds but also paves the way for the rational and efficient development of ideal candidates for energy-saving materials.

physics.chem-ph↗