Zheng Wang, Yahuan Liu, Mingyang Han, Ning Ma, Quanming Lyu, Qingbin Liu and Wen-Hua Sun
{"title":"Efficient transfer hydrogenation of ketones using molybdenum complexes by comprehensively verifying the auxiliary ligands†","authors":"Zheng Wang, Yahuan Liu, Mingyang Han, Ning Ma, Quanming Lyu, Qingbin Liu and Wen-Hua Sun","doi":"10.1039/D2DT01177H","DOIUrl":null,"url":null,"abstract":"<p >Molybdenum complexes ligated with <em>N</em><small><sup>1</sup></small>,<em>N</em><small><sup>1</sup></small>-dialkyl-<em>N</em><small><sup>2</sup></small>-(5,6,7,8-tetrahydroquinolin-8-yl)ethane-1,2-diamines and auxiliary ligands, providing various structural features, were developed: [NN<small><sub>H</sub></small>/NN<small><sub>H</sub></small>N]Mo(CO)<small><sub>4/3</sub></small> (<strong>Mo1–Mo3</strong>), [NN<small><sub>H</sub></small>N]Mo(CO)<small><sub>2</sub></small>Br (<strong>Mo4–Mo5</strong>), [NN<small><sub>H</sub></small>]Mo(CO)(η<small><sup>3</sup></small>-C<small><sub>3</sub></small>H<small><sub>5</sub></small>)Br (<strong>Mo6</strong>) and [NN<small><sub>H</sub></small>N/S]Mo(CO)(PPh<small><sub>3</sub></small>)<small><sub>2</sub></small> (<strong>Mo7–Mo8</strong>). All the complexes were highly active in the transfer hydrogenation (TH) of a model substrate (acetophenone), providing excellent yields of 1-phenylethanol. The structural variation in the ligand framework had a modest effect on the catalyst performance as compared to the changes in the auxiliary ligands Br, PPh<small><sub>3</sub></small> and CO. This structural evolution provided the complex [Mo(NN<small><sub>H</sub></small>)(η<small><sup>3</sup></small>-C<small><sub>3</sub></small>H<small><sub>5</sub></small>)(CO)<small><sub>2</sub></small>Br] (<strong>Mo6</strong>) as the most effective catalyst not only for the transfer hydrogenation of acetophenone but also for a wide range of diverse ketones (up to 43 examples). Moreover, easy purification of the products by only removing the acetone byproduct is another noteworthy feature of this environmentally friendly route.</p>","PeriodicalId":71,"journal":{"name":"Dalton Transactions","volume":" 29","pages":" 10983-10991"},"PeriodicalIF":3.5000,"publicationDate":"2022-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dalton Transactions","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2022/dt/d2dt01177h","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 1
Abstract
Molybdenum complexes ligated with N1,N1-dialkyl-N2-(5,6,7,8-tetrahydroquinolin-8-yl)ethane-1,2-diamines and auxiliary ligands, providing various structural features, were developed: [NNH/NNHN]Mo(CO)4/3 (Mo1–Mo3), [NNHN]Mo(CO)2Br (Mo4–Mo5), [NNH]Mo(CO)(η3-C3H5)Br (Mo6) and [NNHN/S]Mo(CO)(PPh3)2 (Mo7–Mo8). All the complexes were highly active in the transfer hydrogenation (TH) of a model substrate (acetophenone), providing excellent yields of 1-phenylethanol. The structural variation in the ligand framework had a modest effect on the catalyst performance as compared to the changes in the auxiliary ligands Br, PPh3 and CO. This structural evolution provided the complex [Mo(NNH)(η3-C3H5)(CO)2Br] (Mo6) as the most effective catalyst not only for the transfer hydrogenation of acetophenone but also for a wide range of diverse ketones (up to 43 examples). Moreover, easy purification of the products by only removing the acetone byproduct is another noteworthy feature of this environmentally friendly route.
期刊介绍:
Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.