圆锥交点
碱基
完整活动空间
锥面
基准集
交叉口(航空)
基础(线性代数)
原子轨道
分子物理学
计算化学
物理
化学
数学
DNA
量子力学
电子
密度泛函理论
几何学
航空航天工程
生物化学
工程类
作者
Juliana Cuéllar-Zuquin,Ana Julieta Pepino,Ignacio Fdez. Galván,Ivan Rivalta,Francesco Aquilante,Marco Garavelli,Roland Lindh,Javier Segarra‐Martí
标识
DOI:10.1021/acs.jctc.3c00577
摘要
We characterize the photochemically relevant conical intersections between the lowest-lying accessible electronic excited states of the different DNA/RNA nucleobases using Cholesky decomposition-based complete active space self-consistent field (CASSCF) algorithms. We benchmark two different basis set contractions and several active spaces for each nucleobase and conical intersection type, measuring for the first time how active space size affects conical intersection topographies in these systems and the potential implications these may have toward their description of photoinduced phenomena. Our results show that conical intersection topographies are highly sensitive to the electron correlation included in the model: by changing the amount (and type) of correlated orbitals, conical intersection topographies vastly change, and the changes observed do not follow any converging pattern toward the topographies obtained with the largest and most correlated active spaces. Comparison across systems shows analogous topographies for almost all intersections mediating population transfer to the dark 1nO/Nπ* states, while no similarities are observed for the "ethylene-like" conical intersection ascribed to mediate the ultrafast decay component to the ground state in all DNA/RNA nucleobases. Basis set size seems to have a minor effect, appearing to be relevant only for purine-based derivatives. We rule out structural changes as a key factor in classifying the different conical intersections, which display almost identical geometries across active space and basis set change, and we highlight instead the importance of correctly describing the electronic states involved at these crossing points. Our work shows that careful active space selection is essential to accurately describe conical intersection topographies and therefore to adequately account for their active role in molecular photochemistry.
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