The prospects of developing improved models of eumelanin biopolymers and/or novel bioinspired functional materials/scaffolds for application in organoelectronics have incited increasing efforts toward the rational design and synthesis of 5,6-dihydroxyindole (DHI)-based -electron systems with tailored structural and electronic properties.1-3 A valuable entry to this goal has derived from the exploitation of alkynyl chemistry for the assembly of novel oligomers4,5 and the realization of -extended systems
Alkynyl routes to 5,6-dihydroxyindole-based oligomers and functionalized pi-extended scaffolds / Manini, Paola; Pezzella, Alessandro; Napolitano, Alessandra; D'Ischia, Marco. - STAMPA. - (2011), pp. 833-833. (Intervento presentato al convegno XXIV Congresso Nazionale della Società Chimica Italiana tenutosi a Lecce nel 11-16 settembre 2011).
Alkynyl routes to 5,6-dihydroxyindole-based oligomers and functionalized pi-extended scaffolds
MANINI, PAOLA;PEZZELLA, ALESSANDRO;NAPOLITANO, ALESSANDRA;D'ISCHIA, MARCO
2011
Abstract
The prospects of developing improved models of eumelanin biopolymers and/or novel bioinspired functional materials/scaffolds for application in organoelectronics have incited increasing efforts toward the rational design and synthesis of 5,6-dihydroxyindole (DHI)-based -electron systems with tailored structural and electronic properties.1-3 A valuable entry to this goal has derived from the exploitation of alkynyl chemistry for the assembly of novel oligomers4,5 and the realization of -extended systemsI documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
