Excimer formation in a new class of terthiophene-based fluorophores covalently bonded to a cyclotetrasiloxane scaffold has been demonstrated and the photophysical process ruling it has been investigated in detail and modeled theoretically. In contrast to the conventional systems in which long-living fluorophores such as pyrene are linked in the same molecule, an excimer is formed only when two terthiophene-based branches nano-organized on the same cyclotetrasiloxane scaffold are close enough together when excitation takes place. In such a case, excimer formation is extremely efficient, and the new bound excited states are quite stable.

Oligothiophenes nano-organised on a cyclotetrasiloxane scaffold as a model of a silica-bound monolayer: evidence for intramolecular excimer formation

W Mróz;C Botta;A Orbelli Biroli;F De Angelis;L Belpassi;
2009

Abstract

Excimer formation in a new class of terthiophene-based fluorophores covalently bonded to a cyclotetrasiloxane scaffold has been demonstrated and the photophysical process ruling it has been investigated in detail and modeled theoretically. In contrast to the conventional systems in which long-living fluorophores such as pyrene are linked in the same molecule, an excimer is formed only when two terthiophene-based branches nano-organized on the same cyclotetrasiloxane scaffold are close enough together when excitation takes place. In such a case, excimer formation is extremely efficient, and the new bound excited states are quite stable.
2009
Istituto per lo Studio delle Macromolecole - ISMAC - Sede Milano
Inglese
15
12791
12798
http://onlinelibrary.wiley.com/doi/10.1002/chem.200901307/abstract
Sì, ma tipo non specificato
excimers
luminescence
nanostructures
siloxanes
thiophenes
9
info:eu-repo/semantics/article
262
Mróz, W; P Bombenger, J; Botta, C; ORBELLI BIROLI, Alessio; Pizzotti, M; DE ANGELIS, Filippo; Belpassi, L; Tubino, R; Meinardi, F
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/170064
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