Your browser doesn't support javascript.
loading
Chirality Enhancement of Porphyrin Supramolecular Assembly Driven by a Template Preorganization Effect.
Gaeta, Massimiliano; Raciti, Domenica; Randazzo, Rosalba; Gangemi, Chiara M A; Raudino, Antonio; D'Urso, Alessandro; Fragalà, Maria E; Purrello, Roberto.
Afiliação
  • Gaeta M; Department of Chemical Sciences, Università degli Studi di Catania, Viale A. Doria, 6, 95125, Italy.
  • Raciti D; Department of Chemical Sciences, Università degli Studi di Catania, Viale A. Doria, 6, 95125, Italy.
  • Randazzo R; Department of Chemical Sciences, Università degli Studi di Catania, Viale A. Doria, 6, 95125, Italy.
  • Gangemi CMA; Department of Chemical Sciences, Università degli Studi di Catania, Viale A. Doria, 6, 95125, Italy.
  • Raudino A; Department of Chemical Sciences, Università degli Studi di Catania, Viale A. Doria, 6, 95125, Italy.
  • D'Urso A; Department of Chemical Sciences, Università degli Studi di Catania, Viale A. Doria, 6, 95125, Italy.
  • Fragalà ME; Department of Chemical Sciences, Università degli Studi di Catania, Viale A. Doria, 6, 95125, Italy.
  • Purrello R; Department of Chemical Sciences, Università degli Studi di Catania, Viale A. Doria, 6, 95125, Italy.
Angew Chem Int Ed Engl ; 57(33): 10656-10660, 2018 08 13.
Article em En | MEDLINE | ID: mdl-29939459
ABSTRACT
Cationic polylysine promotes, under neutral conditions, the spontaneous aggregation of opposite charged ZnTPPS in water. Spectroscopic investigations evidence a different preorganization of ZnTPPS onto the polypeptide matrix depending on the chain length. Spinodal decomposition theory in confined geometry is used to model this mechanism by considering the time evolution of a homogeneous distribution of randomly adsorbed particles (porphyrins) onto a rodlike polyelectrolyte (polymer) of variable length L.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article