Suppr超能文献

钨二氧代手性配合物——抑制消旋化的计算研究

Chiral-at-Tungsten Dioxo Complexes─A Computational Study on Inhibiting Racemization.

作者信息

Dhimba George, Muller Alfred, Lammertsma Koop

机构信息

Department of Chemical Sciences, University of Johannesburg, Auckland Park, Johannesburg 2006, South Africa.

Department of Chemistry and Pharmaceutical Sciences, Faculty of Sciences, Vrije Universiteit Amsterdam, De Boelelaan 1108, 1081 HZ Amsterdam, The Netherlands.

出版信息

Inorg Chem. 2025 Jul 14;64(27):13569-13576. doi: 10.1021/acs.inorgchem.5c01280. Epub 2025 May 29.

Abstract

Chiral cis-WO(acac) and cis-WO(nacnac) complexes racemize via four pathways according to DFT calculations at ωB97X-D/6-311+G(2d,f) with LANL2DZ for W and with inclusion of acetonitrile solvent. Steric congestion by N-Me and N-Ph substitution of the two nacnac ligands has a substantial geometrical impact and raises the barriers for all pathways. Despite this, even all N-Me and all N-Ph substituted derivatives of cis-WO(nacnac) have the same four channels for racemization. For each of these complexes, the Dhimba-Muller-Lammertsma (DML) twist is preferred over the Conte-Hippler (CH) twist and significantly favored over the established Bailar (B) and Ray-Dutt (RD) twists. The favored DML barrier for WO(nacnac) has a large estimated Δ barrier of 25.7 kcal/mol, suggesting it to be a viable chiral-at-tungsten complex for asymmetric catalysis.

摘要

根据在ωB97X-D/6-311+G(2d,f)水平下的密度泛函理论(DFT)计算,采用LANL2DZ基组描述钨原子,并考虑乙腈溶剂,手性顺式-WO(acac)和顺式-WO(nacnac)配合物通过四种途径发生外消旋化。两个nacnac配体上的N-甲基和N-苯基取代所引起的空间位阻对几何结构有显著影响,并提高了所有途径的能垒。尽管如此,即使是顺式-WO(nacnac)的所有N-甲基和所有N-苯基取代衍生物,也具有相同的四种外消旋化通道。对于这些配合物中的每一种,Dhimba-Muller-Lammertsma(DML)扭转优于Conte-Hippler(CH)扭转,并且明显优于已确立的Bailar(B)扭转和Ray-Dutt(RD)扭转。WO(nacnac)的优势DML能垒估计有25.7 kcal/mol的大Δ能垒,这表明它是一种可行的用于不对称催化的钨手性配合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db16/12264964/0987e0e4aef6/ic5c01280_0001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验