A novel blue-emitting polycyclic aromatic system was synthesized via anion-radical coupling. Its efficient direct hydroxylation led to a phenol possessing an intramolecular hydrogen-bond system. Since the energy gap difference between the enol and keto forms of this molecule is very small, characteristic of ESIPT chromophores, bathochromically shifted fluorescence was not observed.
We have developed a highly optimized methodology that allows for the oxidative acetoxylation of a sterically and electronically demanding library of analogues of benzo[h]quinoline. The optimal conditions for the insertion of an OAc group were identified after examining various reaction parameters (solvent, oxidant, catalyst, temperature, time). The conditions identified (Pd(OAc)(2), PhI(OAc)(2), MeCN, 150 °C, 16 h), combined with the hydrolysis of acetates, resulted in the formation of hydroxybenzoquinolines in 27-59% yield, whereas all previously published procedures were ineffective. This synthesis was compatible with diverse functionalities (ester, aldehyde, carbon-carbon triple bond) and, most importantly, worked for sterically hindered analogues as well as for compounds possessing electron-donating and electron-withdrawing substituents at various positions. All the obtained compounds demonstrated excited-state intramolecular proton transfer (ESIPT) manifesting as small fluorescence quantum yields and large Stokes shifts (8300-9660 cm(-1)). The effect of structural variations in eight 10-hydroxybenzo[h]quinoline analogues on absorption and emission properties was studied in detail.
Eight previously inaccessible derivatives of 10-hydroxybenzo[h]quinoline were prepared via a straightforward strategy comprising formation of the benzo[h]quinoline skeleton followed by C-H acetoxylation at position 10. The occurrence of excited state intramolecular proton transfer (ESIPT) was detected in all cases since emission was observed only from the excited keto-tautomer. Studies on derivatives bearing both electron-donating and electron-withdrawing groups adjacent to the pyridine ring allowed us to identify some design patterns giving rise to NIR emission and large Stokes shifts. For a derivative of 10-hydroxybenzo[c]acridine, emission at 745 nm was observed, one of the lowest energy fluorescence ever reported for ESIPT system. On the basis of time-resolved measurements, proton transfer was found to be extremely fast with time constants in the range (0.08-0.45 ps).
Two previously inaccessible analogs of 10-hydroxybenzo[h]quinoline were prepared via a straightforward strategy comprising the formation of π-expanded phenazines skeleton followed by C-H acetoxylation at position 10. Two bis-phenols possessing C2 and D2 symmetry were obtained in yields of 52% and 15%, respectively. The occurrence of excited state intramolecular proton transfer (ESIPT) was detected in all cases because steady state emission was observed only from the excited keto-tautomer. Additionally, a short-lived, ∼0.1 ps, emission decay was resolved by the femtosecond up-conversion technique at the blue side of the keto-tautomer emission band, 610 nm, and was attributed to the ESIPT, i.e., conversion from enol to keto tautomer. In comparison with the corresponding 10-hydroxybenzo[h]quinoline emissions, the emission spectrum of the π-expanded phenazine analogues were weaker but displayed a characteristic bathochromically shift into NIR region. These phenazine analogues constitute one of largest heterocycles for which ESIPT was unambiguously detected.
Absorption, fluorescence, and fluorescence excitation spectra of 12-hydroxy-1-azaperylene (HAP) and 1-azaperylene were studied in n-alkane matrices at 5 K. Two stable tautomers of HAP, each of them in n-nonane embedded in two sites, were identified and attributed to the enol and keto forms. Theoretical calculations of the energy and vibrational structure of the spectra suggest that tautomer A, with the (0, 0) transition energy at 18,980 ± 10 cm(-1) (and 19,060 ± 10 cm(-1) in the high energy site), should be identified as the keto form, whereas tautomer B, with the (0, 0) energy at 19,200 ± 20 cm(-1) (19,290 ± 20 cm(-1)), as the enol form. Observation of absorption and fluorescence of both tautomeric forms and lack of large Stokes shift of fluorescence of the keto form classify HAP as the limiting case of the excited-state intramolecular proton transfer system.
Meso-substituted corroles bearing directly linked ferrocene unit have been synthesized for the first time. Among various methods studied, only the condensation of pentafluorophenyldipyrromethane with a formylferrocene led to this type of product. A triad containing corrole and porphyrin bridged with ferrocene has been obtained by a convergent approach. Bilanes were used as crucial substrates in the porphyrin-forming step. For the first time it was shown that H 2 O-MeOH-HCl conditions are suitable for preparation of various 10-(formylaryl)corroles via the direct condensation of aromatic dialdehydes with dipyrromethanes. Electrochemical studies of 10-ferrocenyl-5,15-bis(pentafluorophenyl)corrole support the possibility of intramolecular electron transfer from the corrole to the ferrocene system after the electrode oxidation of the ferrocene to a ferrocenium cation. We have studied the structure of 1-(corrolyl)-1 0 -(porphyrinyl)ferrocene by 1 H NMR and UV-Vis. NMR spectra show that this compound has more conformational freedom than analogous, previously studied bis-porphyrinylferrocenes. Absorption spectra suggest the lack of strong electronic interaction between ferrocene and porphyrinoids for dyads and significant conjugation for the triad.
[structure: see text] An unexpected discovery of a novel cyclocondensation reaction of 1,8-diazabicyclo[5.4.0]undec-8-ene (DBU) with activated 1,2-dichloro compounds is described. The 2-aminopyrrole skeleton is generated through the concomitant formation of new nitrogen-carbon and carbon-carbon bonds. A new pentacyclic derivative formed upon the reaction of 2,3-dichloroquinoxaline with DBU exhibits strong fluorescence both in solutions (Phi in hexane = 0.4) and in the solid state.
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