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Polyaniline Doping by ?,?-Difluoro-?-amino Acids.


ABSTRACT: Currently, polyaniline (PANI) is considered as a promising polymer that can be used in biosensors, drug delivery systems, bioelectronics, etc. Its biocompatibility can be strongly improved by using dopants with biofunctionality. This study reveals the protonation/doping of PANI by fluorinated analogs of natural amino acids, namely, ?,?-difluoro-?-amino acids (DFAAs) with alkyl and aromatic tails in N-methylpyrrolidone solutions. We find that these acids can dope PANI due to both the weakened basicity of their amino groups because of two fluorine atoms in ?,?-positions and specific intermolecular interactions (?-? stacking, alkyl-?, F-?) of their tails with units of PANI chains. These interactions did not give the doped PANI salts with high conductivity but led to formation of stable PANI-DFAA complexes, which were confirmed both by clear changes in the UV-Vis and Fourier transform infrared spectra of the protonated/doped PANI and by their conductivity of ?10-6 S/cm. Our results suggest an applicability of such PANI complexes as carriers of DFAA for their biomedical applications.

SUBMITTER: Noskov Y 

PROVIDER: S-EPMC6649075 | biostudies-literature | 2019 Apr

REPOSITORIES: biostudies-literature

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Polyaniline Doping by α,α-Difluoro-β-amino Acids.

Noskov Yuriy Y   Sorochinsky Alexander A   Kukhar Valery V   Pud Alexander A  

ACS omega 20190424 4


Currently, polyaniline (PANI) is considered as a promising polymer that can be used in biosensors, drug delivery systems, bioelectronics, etc. Its biocompatibility can be strongly improved by using dopants with biofunctionality. This study reveals the protonation/doping of PANI by fluorinated analogs of natural amino acids, namely, α,α-difluoro-β-amino acids (DFAAs) with alkyl and aromatic tails in <i>N</i>-methylpyrrolidone solutions. We find that these acids can dope PANI due to both the weake  ...[more]

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