Synthesis and characterization of tunable coumarin- linked glasses as new class of organic/inorganic phosphors
Author(s) -
Alberto Luridiana,
Gianluca Pretta,
Francesco Secci,
Angelo Frongia,
Daniele Chiriu,
Carlo Maria Carbonaro,
Riccardo Corpino,
Pier Carlo Ricci
Publication year - 2014
Publication title -
aip conference proceedings
Language(s) - English
Resource type - Conference proceedings
eISSN - 1551-7616
pISSN - 0094-243X
DOI - 10.1063/1.4900461
Subject(s) - coumarin , quantum yield , fluorescence , covalent bond , phosphor , monolayer , photochemistry , double bond , chemistry , materials science , organic chemistry , nanotechnology , optoelectronics , physics , quantum mechanics
It is well known that stilbene with a trans conformation is highly fluorescent. From the viewpoint of molecular structure, coumarins bear a carbon-carbon double bond which is fixed as trans conformation as in trans-stilbene through a lactone structure. This can help to avoid the trans-cis transformation of the double bond under ultraviolet (UV) irradiation as observed in stilbene compounds and results in strong fluorescence and high fluorescence quantum yield and photostability in most of coumarin derivatives. Herein we report some preliminary results about the synthesis and spectroscopic characterization of tunable coumarins and the development of a new linkage protocol for the obtainment of monolayer coumarin-covalently linked glasses. The resulting organic/inorganic coumarin/silica based Self-Assembled Monolayer (SMA) film is proposed as new phosphors for the substituting of critical raw materials, like rare earths, in photonics applications
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