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dc.contributor.authorViñas, Clara
dc.contributor.authorTarrés, Màrius
dc.contributor.authorGonzález-Cardoso, Patricia
dc.contributor.authorFarràs, Pau
dc.contributor.authorBauduin, Pierre
dc.contributor.authorTeixidor, Francesc
dc.date.accessioned2016-08-12T13:50:32Z
dc.date.available2016-08-12T13:50:32Z
dc.date.issued2013-11-21
dc.identifier.citationVinas, Clara, Tarres, Marius, Gonzalez-Cardoso, Patricia, Farras, Pau, Bauduin, Pierre, & Teixidor, Francesc. (2014). Surfactant behaviour of metallacarboranes. A study based on the electrolysis of water. Dalton Transactions, 43(13), 5062-5068. doi: 10.1039/C3DT52825Aen_IE
dc.identifier.issn1477-9234
dc.identifier.urihttp://hdl.handle.net/10379/5959
dc.description.abstract[3,3′-Co(1,2-C2B9H11)2]−, [1]−, and its chloroderivatives have been described as displaying surfactant/aggregation properties. We have studied their behaviour as electrolytes in the water electrolysis process. The electrolysis experiments support the surfactant behaviour of these compounds. These conclusions have been drawn on the grounds of the intensity/voltage (I/V) curves of water splitting into H2 and O2 of aqueous solutions in which the electrolytes have been tested at the same concentration. The I/V curves have permitted us to map and group the different electrolytes studied in this work. Three differentiated zones have been observed: one for true electrolytes, NO3− and ClO4−; a second one for intermediate electrolytes, BF4− and p-toluenesulfonate (PTS); and a third having the surfactant dodecylbenzenesulfonate (DBS), [1]− and its chloroderivatives. The incorporation into the study of the chloroderivatives of [1]− has allowed us to correlate molecular structure features with aqueous performance. The studied chloroderivatives perform better as electrolytes in accordance with the descending order of available B–H groups. This comes from the higher capacity to generate B–H⋯H–Cc dihydrogen bonds in the non- or less-halogenated molecules, considered one of the main reasons for the generation of the aggregates. In order to generate B–H⋯H–Cc dihydrogen bonds the H–Cc from the carborane cluster is needed. [B12H12]2− was chosen to prove the hypothesis as it has B–H units but lacks H–Cc units. Consequently, it should not produce self-assembling motifs, as is the case. [B12H12]2− has an aqueous behaviour similar to SO42−.en_IE
dc.description.sponsorshipMICINN (CTQ2010-16237), CSIC (I3P grant to P.G.), MEC (FPU grant to M.T.) and the Generalitat de Catalunya 2009/SGR/00279.en_IE
dc.formatapplication/pdfen_IE
dc.language.isoenen_IE
dc.publisherRoyal Society of Chemistryen_IE
dc.relation.ispartofDalton Transactionsen
dc.subjectChemistryen_IE
dc.subjectMetallacarboranesen_IE
dc.subjectWateren_IE
dc.subjectElectrolysisen_IE
dc.titleSurfactant behaviour of metallacarboranes. A study based on the electrolysis of wateren_IE
dc.typeArticleen_IE
dc.date.updated2016-08-10T16:56:52Z
dc.identifier.doi10.1039/C3DT52825A
dc.local.publishedsourcehttp:/dx.doi.org/10.1039/C3DT52825Aen_IE
dc.description.peer-reviewedpeer-reviewed
dc.contributor.funder|~|
dc.internal.rssid9451787
dc.local.contactPau Farras. Email: pau.farrascosta@nuigalway.ie
dc.local.copyrightcheckedNo
dc.local.versionPUBLISHED
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