计算机科学
机器学习
人工智能
匹配(统计)
密度泛函理论
遗传算法
分数(化学)
算法
训练集
反应性(心理学)
集合(抽象数据类型)
学习迁移
计算学习理论
实验数据
数据挖掘
试验装置
基础(线性代数)
计算模型
集成学习
作者
José A Pérez,María M. Zanardi,Ariel M. Sarotti,José A Pérez,María M. Zanardi,Ariel M. Sarotti
标识
DOI:10.1021/acs.jcim.5c02048
摘要
Accurate prediction of Gibbs activation energies (ΔG‡) for Diels-Alder (DA) reactions remains a critical challenge in computational chemistry, as conventional density functional theory (DFT) methods often fail to consistently achieve chemical accuracy (<1 kcal mol-1). In this work, we demonstrate that no single method reliably meets this threshold through a systematic evaluation of 720 DFT approaches across 24 DA reactions. Here, we introduce a proof-of-concept framework that integrates a genetic algorithm and machine learning (GA-ML) to intelligently select cost-effective, multilevel DFT combinations. Our optimized GA1 model identified four low-cost DFT combinations that yield ΔG‡ predictions with a mean absolute error (MAE) of 0.4 kcal mol-1 in both training and external validation sets, matching the accuracy of high-level CCSD(T) calculations at a fraction of the computational cost. To further enhance adaptability, we introduce Dynamic Generalization-Driven Transfer Learning (DGDTL), a novel method that adaptively optimizes linear coefficients, ensuring robust predictions for both known and unseen reactions. The integration of GA-ML and DGDTL establishes a scalable, high-fidelity paradigm for reactivity prediction, with potential applications in catalysis, drug design, and materials science.
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