Two new beta-disubstituted porphyrin-[60]fullerene cyclic bis-adducts have been synthesized using a tetraphenylporphyrin bearing two rigid aldehydic branches directly linked to the same pyrrole ring. The obtained bis-adducts with [60] fullerene have been characterized by mass and NMR spectroscopy.

Tagliatesta, P., Lembo, A., Orlandi, V., Nuccetelli, M. (2010). Synthesis and characterization of new beta-disubstituted porphyrin-[60] fullerene cyclic bis-adducts. JOURNAL OF PORPHYRINS AND PHTHALOCYANINES, 14(8), 727-731 [10.1142/S1088424610002537].

Synthesis and characterization of new beta-disubstituted porphyrin-[60] fullerene cyclic bis-adducts

Tagliatesta, P;Lembo, A;
2010-01-01

Abstract

Two new beta-disubstituted porphyrin-[60]fullerene cyclic bis-adducts have been synthesized using a tetraphenylporphyrin bearing two rigid aldehydic branches directly linked to the same pyrrole ring. The obtained bis-adducts with [60] fullerene have been characterized by mass and NMR spectroscopy.
2010
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore CHIM/03
Settore CHIM/06
English
bis-adducts
fullerene
dyads
Tagliatesta, P., Lembo, A., Orlandi, V., Nuccetelli, M. (2010). Synthesis and characterization of new beta-disubstituted porphyrin-[60] fullerene cyclic bis-adducts. JOURNAL OF PORPHYRINS AND PHTHALOCYANINES, 14(8), 727-731 [10.1142/S1088424610002537].
Tagliatesta, P; Lembo, A; Orlandi, V; Nuccetelli, M
Articolo su rivista
File in questo prodotto:
File Dimensione Formato  
J. Porphyrins and Phthalocyanines 2010, 14, 727 (Synthesis and characterization of new β-disubstituted P-C60 dyad).pdf

solo utenti autorizzati

Tipologia: Versione Editoriale (PDF)
Licenza: Copyright dell'editore
Dimensione 508.36 kB
Formato Adobe PDF
508.36 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

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: https://hdl.handle.net/2108/334246
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 1
  • ???jsp.display-item.citation.isi??? 0
social impact