Five boron-centered spiro compounds with imidazo[1,5-a]pyridin-3-yl phenols as ligands were synthesized and thoroughly characterized through 1H-NMR, 13C-NMR, infrared spectroscopy, and X-ray single crystal analysis. The fluorescence properties of these compounds in solution and in the solid state were investigated, revealing blue emission with wavelengths maxima dependent on the electronic properties of the substituents on the ligands in solution, and an orange-red emission in the solid state. Time-Dependent Density Functional Theory (TD-DFT) calculations were performed to describe the nature of the transitions

Boron-Centered Compounds: Exploring the Optical Properties of Spiro Derivatives with Imidazo[1,5-a]Pyridines

Cinco, Anita;Ardizzoia, G. Attilio;Brenna, Stefano;Colombo, Gioele
2025-01-01

Abstract

Five boron-centered spiro compounds with imidazo[1,5-a]pyridin-3-yl phenols as ligands were synthesized and thoroughly characterized through 1H-NMR, 13C-NMR, infrared spectroscopy, and X-ray single crystal analysis. The fluorescence properties of these compounds in solution and in the solid state were investigated, revealing blue emission with wavelengths maxima dependent on the electronic properties of the substituents on the ligands in solution, and an orange-red emission in the solid state. Time-Dependent Density Functional Theory (TD-DFT) calculations were performed to describe the nature of the transitions
2025
2025
blue emission; boron; fluorescence; spiro compounds
Cinco, Anita; Ardizzoia, G. Attilio; Brenna, Stefano; Therrien, Bruno; Colombo, Gioele
File in questo prodotto:
File Dimensione Formato  
molecules-Spiro_Boron_30-02552-2025.pdf

accesso aperto

Descrizione: Main Text - Open Access
Tipologia: Versione Editoriale (PDF)
Licenza: Creative commons
Dimensione 800.35 kB
Formato Adobe PDF
800.35 kB Adobe PDF Visualizza/Apri

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/11383/2195171
 Attenzione

L'Ateneo sottopone a validazione solo i file PDF allegati

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