2011
DOI: 10.1021/jo2013143
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Site-Selective Imination of an Anthracenone Sensor: Selective Fluorescence Detection of Barium(II)

Abstract: Site-selective imination of anthraquinone-based macrocyclic crown ethers using titanium tetrachloride as the catalyst yields imines where only the external carbonyl group of the anthraquinone forms Schiff-bases. The following aromatic amines yield monomeric compounds (aniline, 4-nitroaniline, 4-pyrrolaniline, and 1,3-phenylenediamine). Reaction of 2 equiv of the macrocyclic anthraquinone host with 1,2- and 1,4-phenylenediamine yields dimeric imine compounds. The 1,2-diimino host acts as a luminescence sensor, … Show more

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Cited by 54 publications
(41 citation statements)
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“…2) The propensity of C=N bond to photoisomerization opens up a non-radiative relaxation pathway. [49][50][51] Both factors may be alleviated through metal coordination at the imino nitrogen, which is described in Section 2.9.…”
Section: Fluorescence Quantum Yieldmentioning
confidence: 99%
“…2) The propensity of C=N bond to photoisomerization opens up a non-radiative relaxation pathway. [49][50][51] Both factors may be alleviated through metal coordination at the imino nitrogen, which is described in Section 2.9.…”
Section: Fluorescence Quantum Yieldmentioning
confidence: 99%
“…12 Selective reduction of the internal carbonyl was achieved using 1.0 equiv of NaBH 4 in aqueous ethanolic solution. Only the more electronegative carbonyl group is reduced leaving the imine group unreacted, even when reduced over a lengthy period of time (15 h).…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…When tested with barium(II) titration in acetonitrile, a linear increase was seen in fluorescence intensity going from 0–133 µM (0 ppm to 18 ppm), after which the sensor molecule saturated. Although there are no other analytical data available, this sensor shows potential for the detection of barium(II) in aqueous media [51].…”
Section: Analytesmentioning
confidence: 99%