Andreas Jörke , Andreas Seidel-Morgenstern , Christof Hamel
{"title":"用operando FTIR光谱研究了铑- biphephos催化的氢甲酰化反应:催化剂活化和速率测定步骤","authors":"Andreas Jörke , Andreas Seidel-Morgenstern , Christof Hamel","doi":"10.1016/j.molcata.2016.10.028","DOIUrl":null,"url":null,"abstract":"<div><p>The homogeneously rhodium catalyzed hydroformylation of 1-decene was studied using operando FTIR spectroscopy. The bulky chelating diphosphite ligand BiPhePhos was used for catalyst modification. Special emphasis was given to the transformation of the Rh-precursor Rh(acac)(CO)<sub>2</sub> to the activated HRh(BiPhePhos)(CO)<sub>2</sub> catalyst. Under hydroformylation conditions, this complex was found to be the most abundant catalyst species over a wide range of olefin conversion. Other inactive or non-selective rhodium species were not detectable. Analysis of the turnover frequency revealed a first order dependence of the hydroformylation rate with respect to the concentration of 1-decene. These findings indicate that the coordination of the olefin to the Rh-BiPhePhos catalyst is determining the hydroformylation rate of 1-decene.</p></div>","PeriodicalId":370,"journal":{"name":"Journal of Molecular Catalysis A: Chemical","volume":"426 ","pages":"Pages 10-14"},"PeriodicalIF":5.0620,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.molcata.2016.10.028","citationCount":"17","resultStr":"{\"title\":\"Rhodium-BiPhePhos catalyzed hydroformylation studied by operando FTIR spectroscopy: Catalyst activation and rate determining step\",\"authors\":\"Andreas Jörke , Andreas Seidel-Morgenstern , Christof Hamel\",\"doi\":\"10.1016/j.molcata.2016.10.028\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The homogeneously rhodium catalyzed hydroformylation of 1-decene was studied using operando FTIR spectroscopy. The bulky chelating diphosphite ligand BiPhePhos was used for catalyst modification. Special emphasis was given to the transformation of the Rh-precursor Rh(acac)(CO)<sub>2</sub> to the activated HRh(BiPhePhos)(CO)<sub>2</sub> catalyst. Under hydroformylation conditions, this complex was found to be the most abundant catalyst species over a wide range of olefin conversion. Other inactive or non-selective rhodium species were not detectable. Analysis of the turnover frequency revealed a first order dependence of the hydroformylation rate with respect to the concentration of 1-decene. These findings indicate that the coordination of the olefin to the Rh-BiPhePhos catalyst is determining the hydroformylation rate of 1-decene.</p></div>\",\"PeriodicalId\":370,\"journal\":{\"name\":\"Journal of Molecular Catalysis A: Chemical\",\"volume\":\"426 \",\"pages\":\"Pages 10-14\"},\"PeriodicalIF\":5.0620,\"publicationDate\":\"2017-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.molcata.2016.10.028\",\"citationCount\":\"17\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Molecular Catalysis A: Chemical\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1381116916304502\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Catalysis A: Chemical","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1381116916304502","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Rhodium-BiPhePhos catalyzed hydroformylation studied by operando FTIR spectroscopy: Catalyst activation and rate determining step
The homogeneously rhodium catalyzed hydroformylation of 1-decene was studied using operando FTIR spectroscopy. The bulky chelating diphosphite ligand BiPhePhos was used for catalyst modification. Special emphasis was given to the transformation of the Rh-precursor Rh(acac)(CO)2 to the activated HRh(BiPhePhos)(CO)2 catalyst. Under hydroformylation conditions, this complex was found to be the most abundant catalyst species over a wide range of olefin conversion. Other inactive or non-selective rhodium species were not detectable. Analysis of the turnover frequency revealed a first order dependence of the hydroformylation rate with respect to the concentration of 1-decene. These findings indicate that the coordination of the olefin to the Rh-BiPhePhos catalyst is determining the hydroformylation rate of 1-decene.
期刊介绍：
The Journal of Molecular Catalysis A: Chemical publishes original, rigorous, and scholarly full papers that examine the molecular and atomic aspects of catalytic activation and reaction mechanisms in homogeneous catalysis, heterogeneous catalysis (including supported organometallic catalysis), and computational catalysis.
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