2021
DOI: 10.37358/rc.20.12.8381
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New Benzo- and Dibenzo-Crown Ethers with (Azulen-1-yl)Vinyl Substituents

Abstract: Several 1-azulenyl vinyl crown ethers were synthesized starting from (1-azulenylmethyl) triphenylphosphonium iodide and 4-formylbenzo-crown ethers in the Wittig reaction conditions. The reaction worked in fair conditions and the obtained mixtures of geometric isomers were separated using column chromatography. The isomers were identified using 1H-NMR spectra and the mass spectra were recorded using ESI. The UV-vis spectra showed bathochromic effect in Z isomer compared with the E one.

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“…The dibenzocrown ether 125 was used as a support for the azulene moieties and the connection between them was realized with spacer C=C or N=N bonds, as described in Scheme 22. The bisvinylazulene 124 was achieved via the Wittig route, starting from the dibenzocrown 125, by passing through the dialdehyde intermediary 126 [53]. The bisazoderivatives 127 was produced via diazotization of the intermediate diamine 128 [54].…”
Section: The Dance Of Two or More Azulenes With Various Spacers ("Dan...mentioning
confidence: 99%
“…The dibenzocrown ether 125 was used as a support for the azulene moieties and the connection between them was realized with spacer C=C or N=N bonds, as described in Scheme 22. The bisvinylazulene 124 was achieved via the Wittig route, starting from the dibenzocrown 125, by passing through the dialdehyde intermediary 126 [53]. The bisazoderivatives 127 was produced via diazotization of the intermediate diamine 128 [54].…”
Section: The Dance Of Two or More Azulenes With Various Spacers ("Dan...mentioning
confidence: 99%