New one-pot synthesis of 4-arylpyrazolo[3,4-b]pyridin-6-ones based on 5-aminopyrazoles and azlactones.

An effective one-pot strategy was developed for the synthesis of 4-arylpyrazolo[3,4-b]pyridin-6-ones from pyrazolo[3,4-b]pyridin-6-ones, obtained by reacting 5-aminopyrazoles with 4-arylidene-2-phenyloxazol-5(4H)-ones (azlactones) under solvent-free conditions, through subsequent elimination of a benzamide molecule in a superbasic medium (t-BuOK/DMSO). The fluorescent properties of the synthesized compounds were studied. 4-Arylpyrazolo[3,4-b]pyridin-6-ones luminesce in the region of 409-440 nm with a quantum yield of 0.09-0.23 when irradiated with UV light.

Synthesis, Photophysical, and (Spectro)Electrochemical Properties of New Benzo[1,2-c][1,2,5]thiadiazoles and Benzo[1,2-d][1,2,3]triazoles Fused with Two Thiazole Rings.

Acylation of benzo[c][1,2,5]thiadiazole-4,7-diamine and 2-hexyl-2H-benzo[d][1,2,3]triazole-4,7-diamine with aromatic acid halides furnished the corresponding N,N'-diamides, which were converted into N,N'-dithioamides by reacting with Lawesson's reagent. A method was developed for the preparation of previously unknown fused systems, dithiazolobenzo[1,2-c][1,2,5]thiadiazoles and dithiazolobenzo[1,2-d][1,2,3]triazoles, by oxidative photochemical cyclization of N,N'-dithioamides. The photophysical and (spectro)electrochemical properties of the obtained compounds and their polymer films electrochemically deposited on ITO were studied. The optical contrast and response time of the synthesized oligomers were determined. The results obtained allow us to consider these substances as promising candidates for electrochromic devices.

Photochemical Synthesis and Electrochemical and Photophysical Properties of 2,7-Diarylbenzo[1,2-d:4,3-d']bis(thiazoles).

This article focuses on the development of practical approaches to the preparation of benzo[1,2-d:4,3-d']bis(thiazoles) using blue light-induced photochemical cyclization of N,N'-(1,4-aryl)dithioamides in the presence of p-chloranil as a mild oxidant. The proposed method allows to obtain benzo[1,2-d:4,3-d']bis(thiazoles) containing donor substituents in the conjugated chain. Photophysical and (spectro)electrochemical properties of 2,6-di([2,2'-bithiophen]-5-yl)benzo[1,2-d:4,3-d']bis(thiazole) and -benzo[1,2-d:4,5-d']bis(thiazole) are studied in detail. The properties of the synthesized compounds suggest their potential applications for organic electronics.

Synthesis of Bis([2,2'-bithiophen]-5-yl)-Substituted Oligothiadiazoles: Effect of the Number of Acceptor Units on Electrochemical and Spectroscopic Properties.

1,3,4-Thiadiazole, 2,2'-bi(1,3,4-thiadiazole), 2,2':5',2″-ter(1,3,4-thiadiazole), and 2,2':5',2″:5″,2‴-quater(1,3,4-thiadiazole) symmetrically disubstituted with 3-alkyl-(2,2'-bithiophen)-5-yl were synthesized by new procedures using readily available ethyl 3-alkyl-(2,2'-bithiophene)-5-carboxylate as a convenient substrate. These new compounds with a fixed number of donor rings and increasing number of acceptor rings showed very interesting, tunable redox properties. In particular, they exhibited electron affinities (EAs) ranging from -3.06 to -3.83 eV, reaching EA values desired for air-operating n-type organic semiconductors. Their electrochemically determined ionization potentials were only moderately dependent on the number of thiadiazole rings, varying from 5.83 to 6.01 eV. Emission spectra of these compounds could also be tuned in a wide range (from 470 to 600 nm). Spectroscopic and electrochemical data were confirmed by density functional theory calculations demonstrating full consistency.

Effect of donor to acceptor ratio on electrochemical and spectroscopic properties of oligoalkylthiophene 1,3,4-oxadiazole derivatives.

A structure-property study across a series of donor-acceptor-donor structures composed of mono- and bi-(1,3,4-oxadiazole) units symmetrically substituted with alkyl functionalized bi-, ter- and quaterthiophene segments is presented. Synthetically tailoring the ratio of electron-withdrawing 1,3,4-oxadiazole to electron-releasing thiophene units and their alkyl grafting pattern permitted us to scrutinize the impact of these structural factors on the redox, absorptive and emissive properties of these push-pull molecules. Contrasting trends of redox potentials were observed, with the oxidation potential closely following the donor-to-acceptor ratio, whereas the reduction potential being tuned independently by either the number of acceptor units or the conjugation length of the donor-acceptor system. Increasing the thiophene unit contribution delivered a shift from blue to green luminescence, while the structural rigidity afforded by intramolecular non-covalent interactions between 1,3,4-oxadiazole and the thiophene moieties has been identified as the prime factor determining the emission efficiency of these molecules. All six structures investigated electro-polymerize easily, yielding electroactive and electrochromic polymers. The polymer doping process is largely influenced by the length of the oligothiophene repeating unit and the alkyl chain grafting density. Polymers with relatively short oligothiophene segments are able to support polarons and polaron-pairs, whereas those with segments longer than six thiophene units could also stabilize diamagnetic charge carries - bipolarons. Increasing the alkyl chain grafting density improved the reversibility and broadened the working potential window of the p-doping process. Stable radical anions have also been investigated, bringing detailed information about the conjugation pattern of these electron-surplus species. This study delivers interesting clues towards the conscious structural design of bespoke frontier energy level oligothiophene functional materials and their polymers by incorporating a structurally matching 1,3,4-oxadiazole unit.

Synthesis and optical properties of new 5'-aryl-substituted 2,5-bis(3-decyl-2,2'-bithiophen-5-yl)-1,3,4-oxadiazoles.

New photoluminescent donor-acceptor-donor (DAD) molecules, namely 5'-aryl-substituted 2,5-bis(3-decyl-2,2'-bithiophen-5-yl)-1,3,4-oxadiazoles were prepared by palladium-catalyzed coupling from readily available compounds such as ethyl 3-decyl-2,2'-bithiophene-5-carboxylate and aryl halides. The obtained compounds feature increasing bathochromic shifts in their emission spectra with increasing aryl-substituent size yielding blue to bluish-green emissions. At the same time, their absorption spectra are almost independent from the identity of the terminal substituent with λmax values ranging from 395 to 405 nm. The observed trends are perfectly predicted by quantum chemical DFT/TDDFT calculations carried out for these new molecules.