L. Rivera-Rivera, Frisia D. Colón-Padilla, Yessenia Ocasio-Delgado, Jomary Martínez-Rivera, Samirah Mercado-Feliciano, C. Ramos, J. E. Cortés-Figueroa
{"title":"Kinetics and Mechanisms of Ligand Exchange Reactions on (Dihapto-Buckminsterfullerene) Pentacarbonyl Tungsten(0)","authors":"L. Rivera-Rivera, Frisia D. Colón-Padilla, Yessenia Ocasio-Delgado, Jomary Martínez-Rivera, Samirah Mercado-Feliciano, C. Ramos, J. E. Cortés-Figueroa","doi":"10.1080/1028662021000062491","DOIUrl":null,"url":null,"abstract":"The Lewis bases triphenyl phosphine and triethyl phosphite (L) displace C 60 from ( m 2 -C 60 )W(CO) 5 to produce the complexes ( m 1 -L)W(CO) 5 . These displacement reactions were studied under conditions where the concentrations of C 60 and L were at least 50 times the concentration of ( m 2 -C 60 )W(CO) 5 . The reactions in various solvents were first order with respect to ( m 2 -C 60 )W(CO) 5 . The pseudo first order rate constant values were independent of the concentration and of the nature of L but dependent on the coordinating ability of the solvent under conditions where [C 60 ]/[L] , 0. Under conditions where 0 h [C 60 ]/[L] h 1, the pseudo first order rate constant values decrease as the values of [C 60 ]/[L] increase. Two limiting cases of an interchange displacement of C 60 from ( m 2 -C 60 )W(CO) 5 , whose relative contributions to the overall mechanism depend on the nature of the solvent, are proposed to be a solvent-assisted C 60 -W(CO) 5 bond displacement and a dissociative displacement. ...","PeriodicalId":54977,"journal":{"name":"Inorganic Reaction Mechanisms","volume":"15 1","pages":"49-56"},"PeriodicalIF":0.0000,"publicationDate":"2002-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Reaction Mechanisms","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/1028662021000062491","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 6
Abstract
The Lewis bases triphenyl phosphine and triethyl phosphite (L) displace C 60 from ( m 2 -C 60 )W(CO) 5 to produce the complexes ( m 1 -L)W(CO) 5 . These displacement reactions were studied under conditions where the concentrations of C 60 and L were at least 50 times the concentration of ( m 2 -C 60 )W(CO) 5 . The reactions in various solvents were first order with respect to ( m 2 -C 60 )W(CO) 5 . The pseudo first order rate constant values were independent of the concentration and of the nature of L but dependent on the coordinating ability of the solvent under conditions where [C 60 ]/[L] , 0. Under conditions where 0 h [C 60 ]/[L] h 1, the pseudo first order rate constant values decrease as the values of [C 60 ]/[L] increase. Two limiting cases of an interchange displacement of C 60 from ( m 2 -C 60 )W(CO) 5 , whose relative contributions to the overall mechanism depend on the nature of the solvent, are proposed to be a solvent-assisted C 60 -W(CO) 5 bond displacement and a dissociative displacement. ...