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

Five boron-centered spiro compounds with imidazo[1,5-<i>a</i>]pyridin-3-yl phenols as ligands were synthesized and thoroughly characterized through <sup>1</sup>H-NMR, <sup>13</sup>C-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.

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Publication Details

Journal
Molecules
Published
2025-06-11
DOI
https://doi.org/10.3390/molecules30122552
Primary Topic
Synthesis and Reactivity of Heterocycles
Type
article
Field-Weighted Citation Impact
0.00

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article

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

Bruno Therrien, Gioele Colombo, Stefano Brenna, Anita Cinco et al.
Molecules
Synthesis and Reactivity of Heterocycles
article

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

Bruno Therrien, Gioele Colombo, Stefano Brenna, Anita Cinco, G. Attilio Ardizzoia
article en

Abstract

Five boron-centered spiro compounds with imidazo[1,5-<i>a</i>]pyridin-3-yl phenols as ligands were synthesized and thoroughly characterized through <sup>1</sup>H-NMR, <sup>13</sup>C-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.

MoleculesVol. 30(12)
University of Insubria (IT), Istituto Universitario di Studi Superiori di Pavia (IT), Consorzio Interuniversitario Reattività Chimica e Catalisi (IT), University of Neuchâtel (CH)
Università degli Studi dell'Insubria, Ministero dell'Università e della Ricerca
Openalex Percentile: Top 90%
Synthesis and Reactivity of Heterocycles
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