Comas-Vilà Gerard, Salvador Pedro
Departament de Química and Institut de Química Computacional i Catàlisi (IQCC), Universitat de Girona, Campus Montilivi s/n, 17071, Girona, Spain.
Chemphyschem. 2024 Sep 16;25(18):e202400582. doi: 10.1002/cphc.202400582. Epub 2024 Jul 19.
Metal-ligand interactions are at the heart of transition metal complexes. The Dewar-Chat-Duncanson model is often invoked, whereby the metal-ligand bonding is decomposed into the simultaneous ligand→metal electron donation and the metal→ligand back-donation. The separate quantification of both effects is not a trivial task, neither from experimental nor computational exercises. In this work we present the effective fragment orbitals (EFOs) and their occupations as a general procedure beyond the Kohn-Sham density functional theory (KS-DFT) framework for the identification and quantification of donor-acceptor interactions, using solely the wavefunction of the complex. Using a common Fe(II) octahedral complex framework, we quantify the σ-donor, π-donor, and π-acceptor character for a large and chemically diverse set of ligands, by introducing the respective descriptors σ, π, and π. We also explore the effect of the metal size, coordination number, and spin state on the donor/acceptor features. The spin-state is shown to be the most critical effect, inducing a systematic decrease of the sigma donation and π-backdonation going from low spin to high spin. Finally, we illustrate the ability of the EFOs to rationalize the Tolman electronic parameter and the trans influence in planar square complexes in terms of these new descriptors.
金属 - 配体相互作用是过渡金属配合物的核心。常被援引的是杜瓦 - 查特 - 邓肯森模型,据此金属 - 配体键合被分解为配体→金属的电子给予和金属→配体的反馈给予同时发生。对这两种效应进行单独量化并非易事,无论是从实验还是计算方面来看。在这项工作中,我们提出了有效片段轨道(EFO)及其占据情况,作为一种超越科恩 - 沙姆密度泛函理论(KS - DFT)框架的通用方法,用于仅使用配合物的波函数来识别和量化供体 - 受体相互作用。使用常见的Fe(II)八面体配合物框架,我们通过引入各自的描述符σ、π和π,对大量化学性质多样的配体的σ供体、π供体和π受体特征进行了量化。我们还探讨了金属尺寸、配位数和自旋态对供体/受体特征的影响。结果表明自旋态是最关键的影响因素,导致从低自旋到高自旋时σ给予和π反馈给予系统性降低。最后,我们说明了EFO能够根据这些新描述符来解释平面正方形配合物中的托尔曼电子参数和反位影响。