The synthesis of three biaryl systems containing the benzo[1,2-b:4,3-b’] framework was accomplished through the Suzuki–Miyaura cross-coupling reaction between 1-bromobenzo[1,2-b:4,3-b’]dithiophene and easily available polycyclic aromatic hydrocarbon boronic acid pinacol esters containing pyrene, fluorene, and fluorenone. The spectroscopic characterization of these molecules was carried out by means of NMR experiments and high-resolution mass spectrometry. UV-vis absorption measurements at different concentrations of the newly synthesized compounds were also performed.

Synthesis and Characterization of Benzo[1,2-b:4,3-b’]dithiophene-Based Biaryls / V. Pelliccioli, L. Ferrari, F. Fagnani, A. Colombo, S. Cauteruccio. - In: MOLBANK. - ISSN 1422-8599. - 2025:1(2025), pp. M1963.1-M1963.8. [10.3390/m1963]

Synthesis and Characterization of Benzo[1,2-b:4,3-b’]dithiophene-Based Biaryls

V. Pelliccioli
;
F. Fagnani;A. Colombo
Penultimo
;
S. Cauteruccio
Ultimo
2025

Abstract

The synthesis of three biaryl systems containing the benzo[1,2-b:4,3-b’] framework was accomplished through the Suzuki–Miyaura cross-coupling reaction between 1-bromobenzo[1,2-b:4,3-b’]dithiophene and easily available polycyclic aromatic hydrocarbon boronic acid pinacol esters containing pyrene, fluorene, and fluorenone. The spectroscopic characterization of these molecules was carried out by means of NMR experiments and high-resolution mass spectrometry. UV-vis absorption measurements at different concentrations of the newly synthesized compounds were also performed.
benzodithiophene; biaryl; Suzuki reaction
Settore CHEM-05/A - Chimica organica
2025
Article (author)
File in questo prodotto:
File Dimensione Formato  
Molbank.pdf

accesso aperto

Tipologia: Publisher's version/PDF
Licenza: Creative commons
Dimensione 1.27 MB
Formato Adobe PDF
1.27 MB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

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/2434/1187280
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 0
  • ???jsp.display-item.citation.isi??? 0
  • OpenAlex 0
social impact