Alkorta Ibon, Montero-Campillo M Merced, Mó Otilia, Elguero José, Yáñez Manuel
Instituto de Química Médica , IQM-CSIC . Juan de la Cierva, 3 , E-28006 Madrid , Spain.
Departamento de Química, Módulo 13, Facultad de Ciencias and Institute of Advanced Chemical Sciences (IadChem) , Universidad Autónoma de Madrid , Campus de Excelencia UAM-CSIC , Cantoblanco, 28049 Madrid , Spain.
J Phys Chem A. 2019 Aug 15;123(32):7124-7132. doi: 10.1021/acs.jpca.9b06051. Epub 2019 Aug 6.
Weak and strong noncovalent interactions such as tetrel bonds and alkaline-earth bonds, respectively, cooperate and get reinforced when acting together in ternary complexes of general formula RN··· SiHF···MY, where MY is a Be or Mg derivative and RN is a N-containing Lewis base with different hybridization patterns. Cooperativity has been studied in the optimized MP2/aug'-cc-pVTZ ternary complexes by looking at changes on geometries, binding energies, Si NMR chemical shifts, and topological features according to the atoms in molecules theoretical framework. Our study shows that cooperativity in terms of energy is in general significant: more than 40 kJ/mol, and up to 83.6 kJ/mol in the most favorable case. The weakest the isolated interaction, the strongest the reinforcement in the ternary complex; in this sense, the tetrel bond is shortened enormously, between 0.3 and 0.6 Å. This dramatic reinforcement of the tetrel bond is also nicely reflected in the positive variations of the Si chemical shifts in all the ternary complexes. At the same time the ternary complexes are characterized by the presence of totally planar silyl group, due to the pentacoordination of the Si atom. Both the hybridization of the N base and the geometry imposed by the alkaline-earth ligands have a strong influence on the binding energies, as they modify the donor ability of N and the Lewis acid character of the alkaline-earth metal.
弱非共价相互作用(如四元键)和强非共价相互作用(如碱土金属键),在通式为RN···SiHF···MY的三元配合物中共同作用时会相互协作并得到增强,其中MY是铍或镁的衍生物,RN是具有不同杂化模式的含氮路易斯碱。根据分子中的原子理论框架,通过观察几何结构、结合能、硅核磁共振化学位移和拓扑特征的变化,在优化的MP2/aug'-cc-pVTZ三元配合物中研究了协同作用。我们的研究表明,从能量角度来看,协同作用通常很显著:超过40 kJ/mol,在最有利的情况下高达83.6 kJ/mol。孤立相互作用越弱,三元配合物中的增强作用越强;从这个意义上说,四元键大幅缩短,在0.3至0.6 Å之间。所有三元配合物中硅化学位移的正向变化也很好地反映了四元键的这种显著增强。同时,由于硅原子的五配位,三元配合物的特征是存在完全平面的硅烷基团。氮碱的杂化以及碱土配体施加的几何结构对结合能都有很大影响,因为它们改变了氮的给体能力和碱土金属的路易斯酸性。