We designed and synthesized a family of molecular switches each pairing an oxazine ring to a chromophoric fragment. Under the influence of either chemical or optical stimulations, the oxazine ring opens to bring the chromophoric appendage in conjugation with either a 3H-indolium cation or a phenolate anion. These structural transformations alter the electronic structure of the chromophore and, as a result, its electrochemical and spectroscopic signatures. Specifically, we demonstrated that the absorption of triphenylamine and thiophene fragments, the fluorescence of a coumarin appendage and the oxidation potential of a ferrocene center can all be switched with acid, base or ultraviolet inputs. Thus, these operating principles and structural designs for switching properties at the molecular level with the aid of external stimulations might eventually lead to a general strategy for the realization of chemo- and photo-responsive materials. (C) 2011 Elsevier B.V. All rights reserved.

Synthesis and properties of molecular switches based on the opening and closing of oxazine rings

SORTINO, Salvatore;
2012

Abstract

We designed and synthesized a family of molecular switches each pairing an oxazine ring to a chromophoric fragment. Under the influence of either chemical or optical stimulations, the oxazine ring opens to bring the chromophoric appendage in conjugation with either a 3H-indolium cation or a phenolate anion. These structural transformations alter the electronic structure of the chromophore and, as a result, its electrochemical and spectroscopic signatures. Specifically, we demonstrated that the absorption of triphenylamine and thiophene fragments, the fluorescence of a coumarin appendage and the oxidation potential of a ferrocene center can all be switched with acid, base or ultraviolet inputs. Thus, these operating principles and structural designs for switching properties at the molecular level with the aid of external stimulations might eventually lead to a general strategy for the realization of chemo- and photo-responsive materials. (C) 2011 Elsevier B.V. All rights reserved.
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/20.500.11769/52503
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 18
  • ???jsp.display-item.citation.isi??? 17
social impact