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hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
dc.contributor.authorRENAULT, Benjamin
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorCLOUTET, Eric
IDREF: 151048681
hal.structure.identifierLaboratoire de Chimie des polymères organiques [LCPO]
hal.structure.identifierTeam 2 LCPO : Biopolymers & Bio-sourced Polymers
dc.contributor.authorCRAMAIL, Henri
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorTASSAING, Thierry
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorBESNARD, Marcel
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2007
dc.identifier.issn1089-5639
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20828
dc.description.abstractEnThe role played by supercritical carbon dioxide used as a dispersant medium in the synthesis of polyurethane particles has been investigated. High-temperature-high-pressure in situ infrared spectroscopic measurements combined with ab initio calculations were performed to investigate the hydroxyl stretching vibrations of ethylene glycol (EG) and 1,4-butanediol (BD), two monomers commonly used in the field of step growth polymerization. Specific interactions between the diols and CO2 have been put in evidence. While the structural characteristics of EG and BD are very similarboth diols have a gauche conformation due to an internal H-bond between the two hydroxyl functionsthey behave differently in the presence of dense CO2. In the case of EG, this internal H-bond is broken, allowing the diol and CO2 to form a complex through the conjunction of a Lewis acid-Lewis base (LA-LB) interaction and a new H-bond. When BD complexes to CO2, this internal H-bond remains and is even reinforced indirectly by the LA-LB interaction occurring between the two moieties. In both cases, such a complex formation induces a polarization of the hydroxyl groups and consequently an increase of their nucleophilicity
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enBASIS-SETS
dc.subject.enACCEPTOR COMPLEXES
dc.subject.enVIBRATIONAL SPECTROSCOPY
dc.subject.enINFRARED-SPECTROSCOPY
dc.subject.enAB-INITIO
dc.subject.enCARBON-DIOXIDE
dc.subject.enETHYLENE-GLYCOL
dc.subject.enMOLECULAR-DYNAMICS
dc.subject.enSPECTRA
dc.subject.enFLUIDS
dc.title.enOn the perturbation of the intramolecular H-bond in diols by supercritical CO2: A theoretical and spectroscopic study
dc.typeArticle de revue
dc.identifier.doi10.1021/jp0673314
dc.subject.halChimie/Polymères
bordeaux.journalJournal of Physical Chemistry A
bordeaux.page4181-4187
bordeaux.volume111
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue20
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00275940
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00275940v1
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