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dc.contributor.authorKang, Sung Ok
dc.contributor.authorLynch, Vincent M.
dc.contributor.authorDay, Victor W.
dc.contributor.authorAnslyn, Eric V.
dc.date.accessioned2017-06-27T19:43:09Z
dc.date.available2017-06-27T19:43:09Z
dc.date.issued2011-10-25
dc.identifier.citationKang, S. O., Lynch, V. M., Day, V. W., & Anslyn, E. V. (2011). Enthalpy vs Entropy Driven Complexation of Homoallylic Alcohols by Rh(I) Complexes. Organometallics, 30(22), 6233–6240. http://doi.org/10.1021/om200793pen_US
dc.identifier.urihttp://hdl.handle.net/1808/24666
dc.descriptionThis document is the Accepted Manuscript version of a Published Work that appeared in final form inOrganometallics, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://doi.org/10.1021/om200793p.en_US
dc.description.abstractThe thermodynamics of binding between several homoallylic alcohols and simple olefinic Rh(I) compounds was examined with 1H NMR spectroscopy and ITC. 1H NMR titrations revealed moderate binding of these alcohols with [Rh(COD)2]+ (1) and [Rh(COD)(CH3CN)2]+ (3), but weaker binding with [Rh(NBD)2]+ (2). ITC indicated that the complexation with [Rh(COD)2]+ is mainly governed by enthalpy whereas binding with [Rh(COD)(CH3CN)2]+ is entirely driven by entropy. The thermodynamic parameters for the homoallylic alcohol binding of Rh(I) complexes 1–3 are consistent with crystallographic data.en_US
dc.publisherAmerican Chemical Societyen_US
dc.titleEnthalpy vs Entropy Driven Complexation of Homoallylic Alcohols by Rh(I) Complexesen_US
dc.typeArticleen_US
kusw.kuauthorDay, Victor W.
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.1021/om200793pen_US
kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC3274780en_US
dc.rights.accessrightsopenAccess


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