Utilizza questo identificativo per citare o creare un link a questo documento:
http://elea.unisa.it/xmlui/handle/10556/3187
Record completo di tutti i metadati
Campo DC | Valore | Lingua |
---|---|---|
dc.contributor.author | De Simone, Nicola Alessandro | - |
dc.date.accessioned | 2019-02-22T12:01:01Z | - |
dc.date.available | 2019-02-22T12:01:01Z | - |
dc.date.issued | 2018-02-22 | - |
dc.identifier.uri | http://hdl.handle.net/10556/3187 | - |
dc.identifier.uri | http://dx.doi.org/10.14273/unisa-1458 | - |
dc.description | 2016 - 2017 | it_IT |
dc.description.abstract | Catalysis is the essence of chemistry as it provides useful tools to make and brake chemical bonds. As nature has been a guide to many scientists, it’s no surprise that in the field of catalysis enzymes were a source of inspiration. Harnessing non covalent interactions, as enzymes do, is a fascinating perspective, and, since supramolecular chemistry became more and more involved in catalysis, a new discipline was born, named supramolecular catalysis. Since supramolecular hosts such as calix[n]arenes have been fruitfully employed in the synthesis of catalysts, in these work we report the design, characterization and applications of new calixarene based catalytic systems. In details chiral calix[4]arene amides 1-7 were employed as phase-transfer catalysts thanks to their cation complexing properties, while the calix[4]arene functionalized with a chiral primary amine-thiourea moiety 8 acted as bifunctional catalyst in several asymmetric conjugate addiction reactions. Finally dinuclear Zirconium-calix[8]arene complex 9 proved to be active in the ring opening polymerization of cyclic esters... [edited by author] | it_IT |
dc.language.iso | en | it_IT |
dc.publisher | Universita degli studi di Salerno | it_IT |
dc.subject | Supramolecular catalysis | it_IT |
dc.subject | Calixarenes | it_IT |
dc.title | Calixarene based catalytic systems | it_IT |
dc.type | Doctoral Thesis | it_IT |
dc.subject.miur | CHIM/06 CHIMICA ORGANICA | it_IT |
dc.contributor.coordinatore | Guerra, Gaetano | it_IT |
dc.description.ciclo | XVI n.s. | it_IT |
dc.contributor.tutor | Neri, Placido | it_IT |
dc.contributor.tutor | Soriente, Annunziata | it_IT |
dc.contributor.tutor | Kohnke, Franz Heinrich | it_IT |
dc.identifier.Dipartimento | Chimica e Biologia "A. Zambelli" | it_IT |
È visualizzato nelle collezioni: | Chimica |
File in questo documento:
File | Descrizione | Dimensioni | Formato | |
---|---|---|---|---|
tesi N. A. De Simone.pdf | tesi di dottorato | 7,3 MB | Adobe PDF | Visualizza/apri |
abstract in inglese N. A. De Simone.pdf | abstract in inglese a cura dell’autore | 349,62 kB | Adobe PDF | Visualizza/apri |
Tutti i documenti archiviati in DSpace sono protetti da copyright. Tutti i diritti riservati.