<rdf:RDF xmlns:crm='http://www.cidoc-crm.org/rdfs/cidoc_crm_v5.0.2_english_label.rdfs#' xmlns:dc='http://purl.org/dc/elements/1.1/' xmlns:dcterms='http://purl.org/dc/terms/' xmlns:doap='http://usefulinc.com/ns/doap#' xmlns:edm='http://www.europeana.eu/schemas/edm/' xmlns:ekt='https://www.semantics.gr/authorities/schemanamespaces/ekt#' xmlns:foaf='http://xmlns.com/foaf/0.1/' xmlns:ore='http://www.openarchives.org/ore/terms/' xmlns:owl='http://www.w3.org/2002/07/owl#' xmlns:rdaGr2='http://rdvocab.info/ElementsGr2/' xmlns:rdf='http://www.w3.org/1999/02/22-rdf-syntax-ns#' xmlns:rdfs='http://www.w3.org/2000/01/rdf-schema#' xmlns:skos='http://www.w3.org/2004/02/skos/core#' xmlns:svcs='http://rdfs.org/sioc/services#' xmlns:wgs84_pos='http://www.w3.org/2003/01/geo/wgs84_pos#' xmlns:xalan='http://xml.apache.org/xalan'><edm:ProvidedCHO rdf:about='https://www.openarchives.gr/aggregator-openarchives/edm/helios/000024-10442_12491'><dc:creator>Martina, Katia</dc:creator><dc:creator>Arena, Francesca</dc:creator><dc:creator>Cravotto, Giancarlo</dc:creator><dc:creator>Χαιρόπουλος, Γεώργιος Α.</dc:creator><dc:creator>Gianolio, Eliana</dc:creator><dc:creator>Barge, Alessandro</dc:creator><dc:creator>Aime, Silvio</dc:creator><dc:description>Bridged cyclodextrin dimers and trimers, in which respectively two and three hydrophobic cavities lie in close proximity, display much higher binding affinities and molecular selectivities than do parent cyclodextrins (CDs). By joining beta CD units with links inserted at different positions (2-2&apos;, 3-2&apos;, 6-2&apos; or 6-2&apos;-6 &apos;&apos;) and interposing spacers of different lengths and shapes, multicavity structures can be synthesized that are precisely tailored to. t specific guest molecules. This enzyme-mimicking strategy can also be used to generate stable supramolecular adducts. A series of CD dimers and trimers was prepared in good yields by carrying out the critical synthetic steps under power ultrasound (US) or microwave (MW) irradiation. Starting from azide and acetylenic CD derivatives, we exploited an efficient MW-promoted Huisgen 1,3-dipolar cycloaddition in the presence of Cu(I) salts. The resulting bridged CD derivatives gave stable adducts with magnetic-resonance-imaging contrast agents (MRI CAs) containing gadolinium(III) chelates. These inclusion complexes were found to be 2 to 3 orders of magnitude more stable than those formed by beta CD and to be endowed with high relaxivity</dc:description><dc:description>Cambridge</dc:description><dc:format>370-379</dc:format><dc:identifier>https://hdl.handle.net/10442/12491</dc:identifier><dc:identifier>1477-0520</dc:identifier><dc:identifier>10.1039/b812172a</dc:identifier><dc:language>eng</dc:language><dc:publisher>Royal Society Chemistry</dc:publisher><dc:rights>© ROYAL SOC CHEMISTRY</dc:rights><dc:rights xml:lang='en'>© ROYAL SOC CHEMISTRY</dc:rights><dc:source>Organic &amp; Biomolecular Chemistry</dc:source><dc:subject rdf:resource='http://semantics.gr/authorities/EKT-voc-classifier/1451294058'></dc:subject><dc:title>New cyclodextrin dimers and trimers capable of forming supramolecular adducts with shape-specific ligands</dc:title><dc:type rdf:resource='http://semantics.gr/authorities/openarchives-item-types/Journal-part'></dc:type><dc:type>Άρθρο σε επιστημονικό περιοδικό</dc:type><dc:type rdf:resource='http://semantics.gr/authorities/openarchives-item-types/Scientific-article'></dc:type><dcterms:created>2009</dcterms:created></edm:ProvidedCHO><skos:Concept rdf:about='http://semantics.gr/authorities/openarchives-item-types/Journal-part'><skos:prefLabel xml:lang='el'>Δημοσίευση σε περιοδικό</skos:prefLabel><skos:prefLabel xml:lang='en'>Publication in journal</skos:prefLabel><skos:broader rdf:resource='http://semantics.gr/authorities/openarchives-item-types/Issue-segment'></skos:broader></skos:Concept><skos:Concept rdf:about='http://semantics.gr/authorities/EKT-voc-classifier/1451294058'><skos:prefLabel xml:lang='el'>Οργανική χημεία</skos:prefLabel><skos:prefLabel xml:lang='en'>Organic Chemistry</skos:prefLabel><skos:broader rdf:resource='http://semantics.gr/authorities/EKT-voc-classifier/1553209112'></skos:broader><skos:exactMatch rdf:resource='http://vocabularies.unesco.org/thesaurus/concept1725'></skos:exactMatch><skos:exactMatch rdf:resource='http://id.loc.gov/authorities/subjects/sh85023022'></skos:exactMatch><skos:exactMatch rdf:resource='http://data.europa.eu/esco/skill/37f621a7-8346-472a-b6fd-a226751a27d8'></skos:exactMatch><skos:exactMatch rdf:resource='http://semantics.gr/authorities/EKT-voc/1451294058'></skos:exactMatch><skos:exactMatch rdf:resource='http://semantics.gr/authorities/LC-gr/organikh-xhmeia'></skos:exactMatch><skos:note xml:lang='en'>isi - Chemistry, Organic includes resources that focus on synthetic and natural organic compounds their synthesis, structure, properties, and reactivity. Research on hydrocarbons, a major area of organic chemistry, is included in this category.</skos:note></skos:Concept><skos:Concept rdf:about='http://semantics.gr/authorities/openarchives-item-types/Scientific-article'><skos:prefLabel xml:lang='el'>Επιστημονικό άρθρο</skos:prefLabel><skos:prefLabel xml:lang='en'>Scientific article</skos:prefLabel><skos:broader rdf:resource='http://semantics.gr/authorities/openarchives-item-types/arthro'></skos:broader></skos:Concept><ore:Aggregation rdf:about='https://www.openarchives.gr/aggregator-openarchives/edm/aggregation/provider/000024-10442_12491%231'><edm:aggregatedCHO rdf:resource='https://www.openarchives.gr/aggregator-openarchives/edm/helios/000024-10442_12491'></edm:aggregatedCHO><edm:dataProvider>Εθνικό Ίδρυμα Ερευνών (ΕΙΕ)</edm:dataProvider><edm:isShownAt rdf:resource='https://helios.eie.gr/helios/handle/10442/12491'></edm:isShownAt><edm:provider>Greek Aggregator OpenArchives.gr | National Documentation Centre (EKT)</edm:provider></ore:Aggregation></rdf:RDF>