2021
DOI: 10.1080/15421406.2021.1933685
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Synthesis and characterization of biphenyl-based azo liquid crystals and its optical properties: effect of lateral and tail group

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Cited by 7 publications
(2 citation statements)
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“…The esterification reaction to protect the acid group of p‐amino benzoic acid was carried out by using ethanol and concentrated H 2 SO 4 to convert ethyl 4‐amino benzoate (A) in 80 % yield [35] . In the second step, the diazotization reaction is performed on compound ( A ) with resorcinol by using NaNO 2 , HCl, and NaOH in an ice bath [36] . The mass volume of the reaction was vigorously mixed for 2 h. At that point, the azo dye product ( B ) conformed by using starch iodide and congo red paper.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The esterification reaction to protect the acid group of p‐amino benzoic acid was carried out by using ethanol and concentrated H 2 SO 4 to convert ethyl 4‐amino benzoate (A) in 80 % yield [35] . In the second step, the diazotization reaction is performed on compound ( A ) with resorcinol by using NaNO 2 , HCl, and NaOH in an ice bath [36] . The mass volume of the reaction was vigorously mixed for 2 h. At that point, the azo dye product ( B ) conformed by using starch iodide and congo red paper.…”
Section: Resultsmentioning
confidence: 99%
“…[35] In the second step, the diazotization reaction is performed on compound (A) with resorcinol by using NaNO 2 , HCl, and NaOH in an ice bath. [36] The mass volume of the reaction was vigorously mixed for 2 h. At that point, the azo dye product (B) conformed by using starch iodide and congo red paper. Further, the alkylation of compound (B) is carried out by the using acetone and alkyl bromides and K 2 CO 3 to convert di-alkoxy phenyl compounds (C 1 -C 4 ) in higher yields.…”
Section: Synthesis and Characterizationmentioning
confidence: 99%