2012
DOI: 10.5155/eurjchem.3.4.461-467.699
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Benzo[g]quinoline heterocyclic derivative as a typical precursor in the synthesis of new class of cyanine-like dyes

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Cited by 9 publications
(5 citation statements)
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References 26 publications
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“…Substitution A = 1-ethyl pyridinium-4-yl salt in dye (4a) by A = 1-ethyl quinolinium-4-yl salt in dye (4b) caused a bathochromic shift of λmax = 75 nm, so compound (4b), exhibited λmax = 520 nm. This back to the more extensive π-delocalization and conjugation within the extra phenyl ring in quinolinium ring in dye (4b) (Table 2) (Ahmed et al, 2018;Gomaa et al, 2012;Shindy et al, 2019;Shindy et al, 2017;Shindy et al, 2015;Soriano et al, 2015;Shindy et al, 2018).…”
Section: Spectral Behavior In 95 % Ethanol Solutionmentioning
confidence: 97%
“…Substitution A = 1-ethyl pyridinium-4-yl salt in dye (4a) by A = 1-ethyl quinolinium-4-yl salt in dye (4b) caused a bathochromic shift of λmax = 75 nm, so compound (4b), exhibited λmax = 520 nm. This back to the more extensive π-delocalization and conjugation within the extra phenyl ring in quinolinium ring in dye (4b) (Table 2) (Ahmed et al, 2018;Gomaa et al, 2012;Shindy et al, 2019;Shindy et al, 2017;Shindy et al, 2015;Soriano et al, 2015;Shindy et al, 2018).…”
Section: Spectral Behavior In 95 % Ethanol Solutionmentioning
confidence: 97%
“…Procedure for the synthesis of 5- ((3-acetyl-1,4-dioxo-1,4-dihydronaphthalen-2yl) diazenyl)-2-hydroxybenzaldehyde (3) Compound (1) (2-acetyl-3-aminonaphthalene-1, 4-dione(1)) and diazonium salt (2) were synthesized according to previous methods [40][41][42].…”
Section: Chemistrymentioning
confidence: 99%
“…Some reactions go through bond breaking, indicating irreversible reaction. For quasi reversible reactions, peak currents not exact proportional [20][21][22][23][24][25][26][27][28][29][30] to .…”
Section: Electro Chemical Behavior Redox Processes For Cubr 2 At Glasmentioning
confidence: 99%