dc.contributor.author | Tatikonda, Rajendhraprasad | |
dc.contributor.author | Bhowmik, Sandip | |
dc.contributor.author | Rissanen, Kari | |
dc.contributor.author | Haukka, Matti | |
dc.contributor.author | Cametti, M. | |
dc.date.accessioned | 2017-04-04T07:52:29Z | |
dc.date.available | 2017-07-15T21:45:08Z | |
dc.date.issued | 2016 | |
dc.identifier.citation | Tatikonda, R., Bhowmik, S., Rissanen, K., Haukka, M., & Cametti, M. (2016). Metallogel formation in aqueous DMSO by perfluoroalkyl decorated terpyridine ligands. <i>Dalton Transactions</i>, <i>45</i>(32), 12756-12762. <a href="https://doi.org/10.1039/c6dt02008a" target="_blank">https://doi.org/10.1039/c6dt02008a</a> | |
dc.identifier.other | CONVID_26134290 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/53471 | |
dc.description.abstract | Terpyridine based ligands 1 and 2, decorated with a C8F17 perfluorinated tag, are able to form stable thermoreversible gels in the presence of several d-block metal chloride salts. The gel systems obtained have been characterized by NMR, X-ray diffraction, electron microscopies and Tgel experiments in order to gain insights into the observed different behaviour of the two similar ligands, also in terms of the effect of additional common anionic species. | |
dc.language.iso | eng | |
dc.publisher | RSC Publications | |
dc.relation.ispartofseries | Dalton Transactions | |
dc.subject.other | metallogel formation | |
dc.subject.other | gelation capabilities | |
dc.subject.other | DMSO | |
dc.title | Metallogel formation in aqueous DMSO by perfluoroalkyl decorated terpyridine ligands | |
dc.type | research article | |
dc.identifier.urn | URN:NBN:fi:jyu-201703291808 | |
dc.contributor.laitos | Kemian laitos | fi |
dc.contributor.laitos | Department of Chemistry | en |
dc.contributor.oppiaine | Epäorgaaninen ja analyyttinen kemia | fi |
dc.contributor.oppiaine | Orgaaninen kemia | fi |
dc.contributor.oppiaine | Soveltava kemia | fi |
dc.contributor.oppiaine | Inorganic and Analytical Chemistry | en |
dc.contributor.oppiaine | Organic Chemistry | en |
dc.contributor.oppiaine | Applied Chemistry | en |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
dc.date.updated | 2017-03-29T15:15:31Z | |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
dc.description.reviewstatus | peerReviewed | |
dc.format.pagerange | 12756-12762 | |
dc.relation.issn | 1477-9226 | |
dc.relation.numberinseries | 32 | |
dc.relation.volume | 45 | |
dc.type.version | acceptedVersion | |
dc.rights.copyright | © 2016 The Royal Society of Chemistry. This is a final draft version of a paper whose final and definitive version is published by RSC Publications. Published in this repository with the kind permission of the publisher. | |
dc.rights.accesslevel | openAccess | fi |
dc.type.publication | article | |
dc.subject.yso | ligandit | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p24741 | |
dc.relation.doi | 10.1039/c6dt02008a | |
dc.type.okm | A1 | |