Electrofluorochromism deals with electrochemical monitoring of luminescence features. There are several reasons to be interested in that field. The first one is the design of displays working in a similar way to electrochromic devices, substituting colors due to absorption with colors due to emission, thus producing much higher brilliance. This requires designing smart molecules and materials, which are likely to exhibit reversible switch of emission by controlling their redox state. There are also a lot of analytical applications, especially in biochemical issues, where in situ dual detection of electrochemical and fluorescence signals can lead to very sensitive and selective biosensors. To achieve this goal, instrumental developments are necessary, involving, among others, beyond diffraction limit and single molecule detection optical techniques. This paper reviews the most recent developments in the above mentioned fields of fluorescence spectroelectrochemistry, coupled detection of fluorescence and electrochemical signals and design of molecules and materials exhibiting electrofluorochromic properties. The first part describes the required features for molecular systems to exhibit a reversible switch in their luminescence properties according to a change in their redox state. Examples among organic and organometallic dyes and redox labelled fluorophores are listed. The second part focuses on the instrumental development in fluorescence spectroelectrochemistry and recent coupling of electrochemical techniques with fluorescence microscopy.Finally, some applications and devices are presented in the last part of this review. This should give an overview of this emerging research field at the interface between physics, chemistry and biology.

New tetrazines substituted by heteroatoms have been synthesized and their electrochemical and photochemical properties investigated. All compounds are reversibly electroactive with standard potentials shifting cathodically according to the donor character of the substituent. The tetrazine derivatives are also fluorescent with maximum emission wavelengths in the range 550-575 nm. Some of them show very long fluorescence lifetimes (several tens of ns) and remain fluorescent in the solid state without major changes in the spectral features. The fluorescence of one of the derivatives can be efficiently quenched by the presence of electron-rich compounds such as triphenylamines, phenol or anisole, which make them very promising compounds for sensor applications.

New fluorescent tetrazines have been prepared and their electrochemistry and fluorescence efficiency evaluated. The occurrence of fluorescence as well as the wavelength were found to be strongly dependent on the substituents, which have to be electronegative heteroatoms. This has been rationalized through a computational study that showed that the crucial factor is the nature of the HOMO, which determines the existence or not of fluorescence. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

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Broad-frequency dielectric behaviors of multiwalled carbon nanotubes ͑MWCNTs͒ embedded in room temperature vulcanization silicone rubber ͑RT-SR͒ matrix were studied by analyzing alternating current ͑ac͒ impedance spectra, which would make a remarkable contribution for understanding some fundamental electrical properties in the MWCNT/RT-SR nanocomposites. Equivalent circuits of the MWCNT/RT-SR nanocomposites were built, and the law of polarization and mechanism of electric conductance under the ac field were acquired. Two parallel RC circuits in series are the equivalent circuits of the MWCNT/RT-SR composites. At different frequency ranges, dielectric parameters including conductivity, dielectric permittivity, dielectric loss, impedance phase, and magnitude present different behaviors.

Several new supramolecular s-tetrazines have been prepared and studied. Their electrochemical and spectroscopic properties have been investigated, especially in the presence of quenchers. Fluorescence quenching has been shown to occur as expected through a charge transfer mechanism and the cyclophane structure has been shown to lead to an acceleration of the quenching process.Scheme 1 Formula of the s-tetrazines.

A facile, efficient and metal-free synthetic approach to 3-monosubstituted unsymmetrical 1,2,4,5-tetrazines is presented. Dichloromethane (DCM) is for the first time recognized as a novel reagent in the synthetic chemistry of tetrazines. Using this novel approach 11 3-aryl/alkyl 1,2,4,5-tetrazines were prepared in excellent yields (up to 75 %). The mechanism of this new reaction, including the role of DCM in the tetrazine ring formation, has been investigated by C labeling of DCM, and is also presented and discussed as well as the photophysical and electrochemical properties.

The study of the chemical and electrochemical fluorescence switching properties of a family of substituted triphenylamine derivatives is reported.