BODIPY Dyes Bearing Multibranched Fluorinated Chains: Synthesis, Structural, and Spectroscopic Studies

Autor: Eduardo Arias, Lorenzo Sori, Simonetta Orlandi, Giancarlo Terraneo, Valentina Dichiarante, Marco Cavazzini, Pierangelo Metrangolo, Francesca Baldelli Bombelli, Andrea Pizzi, Ivana Moggio, Gianluca Pozzi, Maria Isabel Martinez Espinoza
Jazyk: angličtina
Rok vydání: 2019
Předmět:
Zdroj: Chemistry (Weinh., Print) 25 (2019): 9078–9087. doi:10.1002/chem.201901259
info:cnr-pdr/source/autori:Martinez Espinoza, Maria I.; Sori, Lorenzo; Pizzi, Andrea; Terraneo, Giancarlo; Moggio, Ivana; Arias, Eduardo; Pozzi, Gianluca; Orlandi, Simonetta; Dichiarante, Valentina; Metrangolo, Pierangelo; Cavazzini, Marco; Baldelli Bombelli, Francesca/titolo:BODIPY Dyes Bearing Multibranched Fluorinated Chains: Synthesis, Structural, and Spectroscopic Studies/doi:10.1002%2Fchem.201901259/rivista:Chemistry (Weinh., Print)/anno:2019/pagina_da:9078/pagina_a:9087/intervallo_pagine:9078–9087/volume:25
DOI: 10.1002/chem.201901259
Popis: A small series of boron-dipyrromethene (BODIPY) dyes, characterized by the presence of multibranched fluorinated residues, were designed and synthesized. The dyes differ in both the position (para-perfluoroalkoxy-substituted phenyl ring or boron functionalization) and number of magnetically equivalent fluorine atoms (27 or 54 fluorine atoms per molecule). Photophysical and crystallographic characterization of the synthesized BODIPYs was carried out to evaluate the effect of the presence of highly fluorinated moieties on the optical and morphological properties of such compounds.
Databáze: OpenAIRE
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