1379575-16-2Relevant academic research and scientific papers
Diaryl-substituted perylene bis(imides): Synthesis, separation, characterization and comparison of electrochemical and optical properties of 1,7-and 1,6-regioisomer
Dey, Somnath,Efimov, Alexander,Lemmetyinen, Helge
experimental part, p. 2367 - 2374 (2012/05/20)
A series of diaryl-substituted perylene bis(imides) (PBIs) containing electron-donating and-withdrawing aryl groups in the bay region (1-, 6-, 7-and/or 12-positions of the perylene core) were synthesized by Suzuki coupling reaction. The corresponding regioisomers, namely, 1,7-and 1,6-regioisomer, were separated from the mixture by conventional column chromatography without any need of recrystallization. All the individual regioisomers were fully characterized by 1H NMR and HRMS spectroscopy. The compounds were studied by optical spectroscopy and electrochemical techniques. The optical and electrochemical properties of 1,7-regioisomer are slightly different from the 1,6-regioisomer of the respective diaryl-PBI. Significant redshift and broadening of the absorption and emission maxima were observed in all synthesized PBIs depending upon the electronic nature of the attached aryl group. This is very first time such large series of 1,6- diarylperylenetetracarboxydiimides with their corresponding 1,7-regioisomers were synthesized, separated, characterized and studied in detail. 1,7-and 1,6-rsegioisomers of a series of diarylperylenetetracarboxydiimide derivatives were synthesized, separated, and electrochemical and spectroscopic studies have been done in detail. The regioisomers are chromatographically separable and fully characterized by 1H NMR spectroscopy.
Bay region borylation of perylene bisimides
Dey, Somnath,Efimov, Alexander,Lemmetyinen, Helge
supporting information; experimental part, p. 5955 - 5958 (2011/12/14)
Novel bispinacolborane-N,N′-bis(octyl)-3,4,9,10- perylenetetracarboxylic acid bisimide (PBI) was synthesized in high yield. The title compound is a key intermediate in the preparation of PBI aryl derivatives through Suzuki cross-coupling by using a large variety of easily accessible aryl halides. The benign effect of a nonpolar solvent, mild base, and high reaction temperature on the borylation reaction was studied, and the reaction conditions were optimized accordingly. To demonstrate the potential and flexibility of the proposed building block, two corresponding bisarylperylene bisimides were prepared in high yields. For the first time, an efficient and straightforward method was developed for thesynthesis of bis-pinacolborane-N,N′-bis(octyl) -3,4,9,10-perylene tetracarboxylic bisimide derivatives by using a commercially available Pd catalyst. Two Suzuki cross-coupling reactions of novel bispinacolborane perylene derivative are also reported.
