2012
DOI: 10.1016/j.synthmet.2012.02.019
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Peroxidase-mediated synthesis of water-soluble fully sulfonated polyaniline

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Cited by 22 publications
(11 citation statements)
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“…Since the 1980s, various azoarylamines, arylaminoalcohols, arylaminoketones, aminobenzoic acids, and aminobenzenesulfonic acids have successfully been enzymatically polymerized (Table 7 ). The enzymatic polymerization of aminobenzoic acids and aminobenzenesulfonic acids has led to self-doped carboxylated and sulfonated PANIs containing acid moieties in the polymer backbone (Alva et al 1996 , 1997 ; Kim et al 2006a , b , 2007b ; Román et al 2012 ). Polyanionic templates were found to be unsuitable for the enzymatic polymerization of acid-functionalized aniline derivatives (Kim et al 2006a ).…”
Section: Enzymatic Polymerization Of Substituted Anilines and Other Amentioning
confidence: 99%
“…Since the 1980s, various azoarylamines, arylaminoalcohols, arylaminoketones, aminobenzoic acids, and aminobenzenesulfonic acids have successfully been enzymatically polymerized (Table 7 ). The enzymatic polymerization of aminobenzoic acids and aminobenzenesulfonic acids has led to self-doped carboxylated and sulfonated PANIs containing acid moieties in the polymer backbone (Alva et al 1996 , 1997 ; Kim et al 2006a , b , 2007b ; Román et al 2012 ). Polyanionic templates were found to be unsuitable for the enzymatic polymerization of acid-functionalized aniline derivatives (Kim et al 2006a ).…”
Section: Enzymatic Polymerization Of Substituted Anilines and Other Amentioning
confidence: 99%
“…Interestingly, deposition of Ag NPs on the hd‐MSN‐NH 2 nanoparticles showed the decrease in the binding energy values of 3d doublet as compared to their standard values in bulk silver (368.2 eV and 375.2 eV) . The high resolution spectrum of N 1s of hd‐MSN‐NH 2 showed two peaks at 395 eV and 398.4 eV corresponding to N−H and N−C bonding respectively …”
Section: Resultsmentioning
confidence: 97%
“…For example, it was found in a number of studies that substituted aniline containing a sulfo and alkoxysulfo group did not undergo electropolymerization. 35,[75][76][77] In order to prevent the overoxidation of the polymer lm, the anodic limit of the polymerization potential during the electrosynthesis of functionalized high molecular mass anilines is maintained at low values. At the initial stages of the process, the PANI lm grows slowly, but aer about 20 cycles this process accelerates signicantly and approaches completion aer 50 cycles at a scan rate of 10-100 mV s À1 , which indicates its low electrical conductivity.…”
Section: Electrochemical Synthesismentioning
confidence: 99%
“…The yield of the target product in the synthesis described above is no higher than 50%. 37,47,[74][75][76][77][78][79][80][81][82] Despite the simplicity of the experiment, it appears that the low popularity of this method for synthesizing high molecular mass compounds is explained by the low product yields.…”
Section: Interface Polymerizationmentioning
confidence: 99%
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