A metal organic framework (MOF) based on the [Cu(4)I(4)DABCO(2)] cluster (DABCO = 1,4-diazabicyclo[2.2.2]octane), MOF 1, shows bright emission with a maximum at 556 nm and an emission quantum yield of 0.53 in the solid state. When the large cavities of the MOF are loaded during the synthesis with different amounts of ferrocene {FeCp2, [((5)-C5H5)(2)Fe-II]}, the luminescence of MOF 1 decreases with the increase in the ferrocene content, reaching an almost complete quenching for 3.5 wt.-% of cage loading, corresponding to the complete filling of the MOF cavities. When an electric potential is applied to the FeCp2@MOF 1 deposited onto an ITO glass, the (FeCp2)-Cp-II is oxidised to (FeCp2+)-Cp-III, and the MOF 1 emission is partially switched on again, indicating that a photoinduced electron-transfer reaction is contributing to the quenching process.

Switch On/Switch Off Signal in an MOF-Guest Crystalline Device

Barbieri;Andrea;Ventura;Barbara
2013

Abstract

A metal organic framework (MOF) based on the [Cu(4)I(4)DABCO(2)] cluster (DABCO = 1,4-diazabicyclo[2.2.2]octane), MOF 1, shows bright emission with a maximum at 556 nm and an emission quantum yield of 0.53 in the solid state. When the large cavities of the MOF are loaded during the synthesis with different amounts of ferrocene {FeCp2, [((5)-C5H5)(2)Fe-II]}, the luminescence of MOF 1 decreases with the increase in the ferrocene content, reaching an almost complete quenching for 3.5 wt.-% of cage loading, corresponding to the complete filling of the MOF cavities. When an electric potential is applied to the FeCp2@MOF 1 deposited onto an ITO glass, the (FeCp2)-Cp-II is oxidised to (FeCp2+)-Cp-III, and the MOF 1 emission is partially switched on again, indicating that a photoinduced electron-transfer reaction is contributing to the quenching process.
2013
Istituto per la Sintesi Organica e la Fotoreattivita' - ISOF
MOF
Luminescence
Crystalline device
Electrochemistry
Host-guest
Copper
METAL-ORGANIC FRAMEWORKS
ELECTRON-TRANSFER
PHOTOPHYSICAL PROPERTIES
LUMINESCENCE
FERROCENE
TETRANUCLEAR
DERIVATIVES
HOST
ABSORPTION
CHEMISTRY
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/219988
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