Materials in which photoluminescence is modulated by redox processes are known as electrofluorochromic. Intrinsically switchable fluorophores, incorporating both redox and fluorescent moieties, could be ideal electrofluorochromic materials if they possess high fluorescence quantum yields in at least one of their redox states. Fluorescent liquid crystals with redox active centres could combine the above requirements with the advantage to work in bulk anisotropic phases. However, electrofluorochromic liquid crystals have not been reported yet because their synthesis is challenging due to aggregation-caused fluorescent quenching. Here we show the first examples of electrofluorochromic p-conjugated ionic liquid crystals based on thienoviologens. These ordered materials, combining ionic and electronic functions, are highly fluorescence in the bulk state (quantum yield460%). Their direct electrochemical reduction leads to fast and reversible bulk electrofluorochromic response in both columnar and smectic phases allowing for fluorescence intensity modulation and colour tuning.

A highly fluorescent electrofluorochromic gel with quantum yields as high as 67% is prepared by incorporating the thienoviologen fluorophore 4,4′‐(2,2′‐bithiophene‐5,5′‐diyl)bis(1‐nonylpridinium)bistriflimide into a polymeric matrix. The fluorescent emission spectrum of the gel at low percentages of thienoviologen shows a strong band at 530 nm. A new intense fluorescence band at 630 nm can be induced by fluorophore aggregation. Single layer electrofluorochromic devices were readily prepared by sandwiching the polymer gels between two indium tin oxide (ITO) electrodes. The fluorescence intensity can be easily modulated between a fluorescent and a quenched state, in a wide visible spectral range, by direct electrochemical reduction of the thienoviologen fluorophore. It exhibits three reduction states, each with different emission properties. The reversible interconversion among these states leads to a high electrofluorochromic stability of the device, exhibiting switching times of a few seconds and, to the best of our knowledge, the highest contrast ratio (337).

Herein we present organic mixed-valence compounds with an innovative H-shape design, where four redox centres are bridged "vertically" via a dibenzofulvene backbone and "horizontally" via a bis-(dibenzofulvene)-thiophene bridge. These compounds are easily oxidized to stable highly charged radical species which show intense intervalence charge transfer transitions in the near infrared region. Interestingly, depending on the position of the arylamine substituents on the bridge, both vertical and horizontal electron transfer pathways can be optically induced.

The thienoviologen series 4,4'-(2,2'-bithiophene-5,5'-diyl)bis(1-alkylpridinium)X2, with = counterion is a new class of electron acceptor materials which show very interesting electrochromic and electrofluorescence properties. Depending on the length, m, of the promesogenic alkyl chains, and on the counterion, thienoviologens might become liquid crystals. Here, we present the mesomorphic behaviour, and the electrochemical and spectroelectrochemical properties in solution of new thienoviologens of the series and (I = iodide; NTf2(-) = bis(tri-fuoromethylsulfonyl)imide) with m = 8, 12. Interestingly, we found that only the compounds are liquid crystals, exhibiting a calamitic behaviour in contrast to the homologous compounds of the series with m = 9-11 and X = NTf2(-), which showed columnar rectangular mesophases. The electrochemical study here reported allowed us to explain for the first time the anomalous behaviour of these thienoviologens already observed in cyclic voltammetry, where two apparently irreversible redox processes occur. This can be explained by a comproportionation reaction in which the neutral species rapidly reduces the dication to the radical-cation, due to its strong reducing power. Electrochemical reduction of the thienoviologens causes electrochromism since a new absorption band, occurring at 660 nm in the electronic spectra, appears with the negative potential bias applied. With a LUMO level of 3.64 eV, similar to those of the C60 and of other n-type materials, these compounds can find applications in several electronics devices, where their liquid crystalline properties can be used to control film morphology and geometry, provided they have good electron mobility.

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Thienosquaraines are an interesting class of electroactive dyes that are useful for applications in organic electronics. Herein, the redox chemistry and electrochromic response of a few newly synthesized thienosquaraines are presented. These properties are compared to those of the commercial 2,4-bis[4-(N,N-diisobutylamino)-2,6-dihydroxyphenyl]squaraine. The stability of the radical ions formed in electrochemical processes strongly affects these properties, as shown by cyclic voltammetry, in situ spectroelectrochemistry, and quantum chemical calculations. Furthermore, all of the dyes show aggregation tendency resulting in panchromatic absorption covering the whole UV/Vis spectral range.

π-Conjugated ionic liquid crystals are a very interesting class of salts where the coupling of ionic and electronic functions with the anisotropy typical of liquid crystals may give rise to materials with advanced bulk properties. Defect-free active thin films obtainable by simplemesophase self-assembly of these materials may be exploited in a number of different electro-optical devices. Here we show that the rich mesomorphism of the thienoviologen salts 4,4′-(2,2′-bithiophene-5,5′-diyl)bis(1-alkylpyridinium), which includes smectic, columnar, and nematic phases, significantly depends on the counterion type and the length of the promesogenic alkyl chains, highlighting the delicate balance among ion/ion, π−π stacking, and hydrophobic interactions. These salts show notable fluorescence properties in the bulk, strongly dependent on the self-assembling