An enzymatic biomimetic system: enhancement of catalytic efficiency with new polymeric chiral ionic liquids synthesised by controlled radical polymerisation
Impacte
Scholar |
Altres documents de l'autoria: Karjalainen, Erno; Izquierdo Henríquez, Diana F.; Martí-Centelles, Vicente; Luis, Santiago V.; Tenhu, Heikki; Garcia-Verdugo, Eduardo
Metadades
Mostra el registre complet de l'elementcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/7053
comunitat-uji-handle3:10234/8639
comunitat-uji-handle4:
INVESTIGACIONAquest recurs és restringit
http://dx.doi.org/10.1039/c3py01364b |
Metadades
Títol
An enzymatic biomimetic system: enhancement of catalytic efficiency with new polymeric chiral ionic liquids synthesised by controlled radical polymerisationAutoria
Data de publicació
2014Editor
Royal Society of ChemistryISSN
1759-9954; 1759-9962Cita bibliogràfica
Polym. Chem., 2014, 5, 1437Tipus de document
info:eu-repo/semantics/articleVersió de l'editorial
http://pubs.rsc.org/en/content/articlepdf/2014/py/c3py01364bResum
The controlled radical polymerization of monomeric units containing chiral ionic liquids (CILs) allows the
synthesis of intrinsically chiral polymers through a bottom-up design. These polymeric chiral ionic liquids ... [+]
The controlled radical polymerization of monomeric units containing chiral ionic liquids (CILs) allows the
synthesis of intrinsically chiral polymers through a bottom-up design. These polymeric chiral ionic liquids
(PCILs) show a well-defined three dimensional structure organized as the result of a complex noncovalent
network of hydrogen-bonding contacts driven by the C2 hydrogen atoms of the imidazolium
aromatic rings and the OH moieties present in the side functionalities of the main polymeric chain. The
exchange of the chloride counter ion by the L-prolinate anion leads to new types of polymeric catalysts,
which behave as efficient artificial aldolase biomimetic systems, being highly active and selective for
the aldol reaction in water. These new polymeric catalysts are significantly more active than the
corresponding monomeric counterpart when the reaction is performed either in water or in the
presence of water. The increase in catalytic efficiency can be related to their 3D structure, displaying
helical chirality in the polymeric chain as a function of their preparation methodology. Under suitable
experimental conditions, these polymers are able to catalyse the consecutive aldol-dehydration process,
behaving as synthetic mimics of the aldolase-dehydrogenase enzymatic system. Moderate
enantioselectivities can be achieved under suitable conditions. [-]
Publicat a
Polym. Chem., 2014, 5, 1437–1446Drets d'accés
This journal is © The Royal Society of Chemistry 2014
http://rightsstatements.org/vocab/InC/1.0/
info:eu-repo/semantics/restrictedAccess
http://rightsstatements.org/vocab/InC/1.0/
info:eu-repo/semantics/restrictedAccess
Apareix a les col.leccions
- QUIO_Articles [702]