2015
DOI: 10.1039/c5nj01828e
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Ethanol-guided synthesis of (flower-on-leaf)-like aniline oligomers with excellent adsorption properties

Abstract: A novel oligoaniline with hierarchical flower-on-leaf microstructures has been fabricated via the oxidation of aniline in EtOH/water (3 : 7, v/v) mixtures. The as-prepared oligoaniline was characterized using the UV-vis, FTIR, 1 H NMR and MALDI-TOF MS techniques for analyzing the chemical structures.A possible formation mechanism has been proposed to interpret the growth of such hierarchical microstructures, and several inter-molecular interactions were suggested to drive the supermolecular assembly. The effec… Show more

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Cited by 11 publications
(12 citation statements)
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“…Furthermore, the formation of oxygen-containing products (arylhydroxylamine, nitrosoarene, nitroarene, azoxyarene, amino-phenols, benzoquinones, and oligomers containing such structures) is also possible (Ćirić-Marjanović 2013b; Kříž et al 2011; Surwade et al 2009; Zhou et al 2015). The main product as well as the product distribution after the reaction is completed are very dependent on the reaction conditions: this includes such characteristics like the type of oxidant, the concentration of the oxidant, the concentration of the arylamine, the ratio between the oxidant and the arylamine, the solvent type, the presence of co-solvent, the ratio between the solvent and the co-solvent, and the presence and concentration of reaction-controlling templates (Ćirić-Marjanović 2013b; Rakić et al 2015; Walde and Guo 2011).…”
Section: Introductionmentioning
confidence: 99%
“…Furthermore, the formation of oxygen-containing products (arylhydroxylamine, nitrosoarene, nitroarene, azoxyarene, amino-phenols, benzoquinones, and oligomers containing such structures) is also possible (Ćirić-Marjanović 2013b; Kříž et al 2011; Surwade et al 2009; Zhou et al 2015). The main product as well as the product distribution after the reaction is completed are very dependent on the reaction conditions: this includes such characteristics like the type of oxidant, the concentration of the oxidant, the concentration of the arylamine, the ratio between the oxidant and the arylamine, the solvent type, the presence of co-solvent, the ratio between the solvent and the co-solvent, and the presence and concentration of reaction-controlling templates (Ćirić-Marjanović 2013b; Rakić et al 2015; Walde and Guo 2011).…”
Section: Introductionmentioning
confidence: 99%
“…2(a)) presents absorption bands at 275 and 386 nm, indicating that aniline oligomers were formed. 26,31 The absorption at 275 nm could be attributed to the -* transition in aniline, given the presence of a residual monomer in the product, while the band at 386 nm might be due to molecules with a phenazine-like structure. 26 Besides, the weak n-* shoulder at about 525 is also observed in the spectrum, which should correspond to linear oligomers.…”
Section: Resultsmentioning
confidence: 99%
“…The UV–Vis spectrum (Fig. (a)) presents absorption bands at 275 and 386 nm, indicating that aniline oligomers were formed , . The absorption at 275 nm could be attributed to the π –π* transition in aniline, given the presence of a residual monomer in the product, while the band at 386 nm might be due to molecules with a phenazine‐like structure .…”
Section: Resultsmentioning
confidence: 99%
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