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Nat. Comput. Sci. | 面向未见化学反应的鲁棒生成式过渡态模型

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TL;DR - A Nature Computational Science study finds generative transition-state models fail sharply on unseen elements and catalysts. Self-supervised pretraining on inexpensive equilibrium conformations improves out-of-distribution accuracy while reducing required reaction data by up to 75%.

  • New benchmarks cover periodic-group substitutions and 10 transition metals, exposing severe element-specific generalization failures in React-OT and AEFM.
  • Pseudo-reaction pretraining reduced median RMSD from 0.39 Å to 0.19 Å for structurally similar reactions containing unseen transition metals.
  • Semi-empirical GFN2-xTB data enabled economical domain adaptation, but generated structures still require DFT optimization to verify first-order saddle points.
  • The approach separates learning target-domain chemical geometry from learning reaction mechanisms with scarce transition-state data.

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Nat. Comput. Sci. | 面向未见化学反应的鲁棒生成式过渡态模型

WeChat: DrugAI 2026-08-14 doi:10.1038/s43588-026-01034-5
Public signals OpenAlex citations 1
Providers: Hugging Face · N/A OpenAlex · Citations 1 Publisher · N/A Semantic Scholar · N/A X · N/A Fetched 2026-09-15 14:32:39.994947 UTC

TL;DR - A Nature Computational Science study finds generative transition-state models fail sharply on unseen elements and catalysts. Self-supervised pretraining on inexpensive equilibrium conformations improves out-of-distribution accuracy while reducing required reaction data by up to 75%.

  • New benchmarks cover periodic-group substitutions and 10 transition metals, exposing severe element-specific generalization failures in React-OT and AEFM.
  • Pseudo-reaction pretraining reduced median RMSD from 0.39 Å to 0.19 Å for structurally similar reactions containing unseen transition metals.
  • Semi-empirical GFN2-xTB data enabled economical domain adaptation, but generated structures still require DFT optimization to verify first-order saddle points.
  • The approach separates learning target-domain chemical geometry from learning reaction mechanisms with scarce transition-state data.
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