{"title":"Chiral-at-Tungsten Dioxo Complexes─A Computational Study on Inhibiting Racemization","authors":"George Dhimba, Alfred Muller, Koop Lammertsma","doi":"10.1021/acs.inorgchem.5c01280","DOIUrl":null,"url":null,"abstract":"Chiral cis-WO<sub>2</sub>(acac)<sub>2</sub> and cis-WO<sub>2</sub>(nacnac)<sub>2</sub> 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<sub>2</sub>(nacnac)<sub>2</sub> 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<sub>2</sub>(nacnac)<sub>2</sub><sup>Ph4</sup> has a large estimated Δ<i>G</i> barrier of 25.7 kcal/mol, suggesting it to be a viable chiral-at-tungsten complex for asymmetric catalysis.","PeriodicalId":40,"journal":{"name":"Inorganic Chemistry","volume":"19 1","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.inorgchem.5c01280","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
Chiral cis-WO2(acac)2 and cis-WO2(nacnac)2 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-WO2(nacnac)2 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 WO2(nacnac)2Ph4 has a large estimated ΔG barrier of 25.7 kcal/mol, suggesting it to be a viable chiral-at-tungsten complex for asymmetric catalysis.
期刊介绍:
Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.