New [1,3]thiazolo[3,2-b][1,2,4]triazol-7-ium cationic surfactant as a stabilizer of silver and gold nanoparticles

A new [1,3]thiazolo[3,2- b ][1,2,4]triazol-7-ium-based cationic surfactant was examined as a stabilizer in the “wet chemistry” synthesis of silver and gold nanoparticles (NPs). The synthesis of the new [1,3]thiazolo[3,2- b ][1,2,4]triazol-7-ium cationic surfactant was performed via the reaction of p...

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Published in:Applied nanoscience Vol. 13; no. 7; pp. 5079 - 5090
Main Authors: Fizer, Maksym M., Fizer, Oksana I., Slivka, Mikhailo V., Mariychuk, Ruslan T.
Format: Journal Article
Language:English
Published: Cham Springer International Publishing 01-07-2023
Springer Nature B.V
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Abstract A new [1,3]thiazolo[3,2- b ][1,2,4]triazol-7-ium-based cationic surfactant was examined as a stabilizer in the “wet chemistry” synthesis of silver and gold nanoparticles (NPs). The synthesis of the new [1,3]thiazolo[3,2- b ][1,2,4]triazol-7-ium cationic surfactant was performed via the reaction of proton-induced cyclization of 5-heptadecyl-4-methyl-3-methallylsulfanyl-1,2,4-triazole. The new heterocyclic surfactant was explored as a stabilizer in an efficient synthesis of silver and gold NPs from silver nitrate and tetrachloroauric acid. The structure of the new [1,3]thiazolo[3,2- b ][1,2,4]triazol-7-ium surfactant was analyzed by Fourier transformed infrared spectroscopy, nuclear magnetic resonance (on 1 H and 13 C nucleus), and with density functional theory calculations at the PBE0/def2-SVP/def2-TZVP(Ag/Au) level of theory. The NPs’ solutions were characterized by UV–Vis spectroscopy. The electronic structure and stabilization ability of [1,3]thiazolo[3,2- b ][1,2,4]triazol-7-ium cation were compared with the characteristics of cetylpyridinium. 2-Heptadecyl-3,6,6-trimethyl-5,6-dihydro-3 H -[1,3]thiazolo[3,2- b ][1,2,4]triazol-7-ium perchlorate can be used as a stabilizer to synthesize Ag–, Au–, and Ag–Au-NPs. Quantum chemical modeling clearly shows a preferable association of metal NP anions (Ag 15 − and Au 15 − ) with the cationic surfactant.
AbstractList A new [1,3]thiazolo[3,2- b ][1,2,4]triazol-7-ium-based cationic surfactant was examined as a stabilizer in the “wet chemistry” synthesis of silver and gold nanoparticles (NPs). The synthesis of the new [1,3]thiazolo[3,2- b ][1,2,4]triazol-7-ium cationic surfactant was performed via the reaction of proton-induced cyclization of 5-heptadecyl-4-methyl-3-methallylsulfanyl-1,2,4-triazole. The new heterocyclic surfactant was explored as a stabilizer in an efficient synthesis of silver and gold NPs from silver nitrate and tetrachloroauric acid. The structure of the new [1,3]thiazolo[3,2- b ][1,2,4]triazol-7-ium surfactant was analyzed by Fourier transformed infrared spectroscopy, nuclear magnetic resonance (on 1 H and 13 C nucleus), and with density functional theory calculations at the PBE0/def2-SVP/def2-TZVP(Ag/Au) level of theory. The NPs’ solutions were characterized by UV–Vis spectroscopy. The electronic structure and stabilization ability of [1,3]thiazolo[3,2- b ][1,2,4]triazol-7-ium cation were compared with the characteristics of cetylpyridinium. 2-Heptadecyl-3,6,6-trimethyl-5,6-dihydro-3 H -[1,3]thiazolo[3,2- b ][1,2,4]triazol-7-ium perchlorate can be used as a stabilizer to synthesize Ag–, Au–, and Ag–Au-NPs. Quantum chemical modeling clearly shows a preferable association of metal NP anions (Ag 15 − and Au 15 − ) with the cationic surfactant.
A new [1,3]thiazolo[3,2-b][1,2,4]triazol-7-ium-based cationic surfactant was examined as a stabilizer in the “wet chemistry” synthesis of silver and gold nanoparticles (NPs). The synthesis of the new [1,3]thiazolo[3,2-b][1,2,4]triazol-7-ium cationic surfactant was performed via the reaction of proton-induced cyclization of 5-heptadecyl-4-methyl-3-methallylsulfanyl-1,2,4-triazole. The new heterocyclic surfactant was explored as a stabilizer in an efficient synthesis of silver and gold NPs from silver nitrate and tetrachloroauric acid. The structure of the new [1,3]thiazolo[3,2-b][1,2,4]triazol-7-ium surfactant was analyzed by Fourier transformed infrared spectroscopy, nuclear magnetic resonance (on 1H and 13C nucleus), and with density functional theory calculations at the PBE0/def2-SVP/def2-TZVP(Ag/Au) level of theory. The NPs’ solutions were characterized by UV–Vis spectroscopy. The electronic structure and stabilization ability of [1,3]thiazolo[3,2-b][1,2,4]triazol-7-ium cation were compared with the characteristics of cetylpyridinium. 2-Heptadecyl-3,6,6-trimethyl-5,6-dihydro-3H-[1,3]thiazolo[3,2-b][1,2,4]triazol-7-ium perchlorate can be used as a stabilizer to synthesize Ag–, Au–, and Ag–Au-NPs. Quantum chemical modeling clearly shows a preferable association of metal NP anions (Ag15− and Au15−) with the cationic surfactant.
Author Fizer, Maksym M.
Slivka, Mikhailo V.
Fizer, Oksana I.
Mariychuk, Ruslan T.
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Keywords Metal nanoparticles
1,2,4-Triazole
Gold nanoparticles
Density functional theory
Reactivity descriptors
Surfactant
Silver nanoparticles
1,3-Thiazole
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Snippet A new [1,3]thiazolo[3,2- b ][1,2,4]triazol-7-ium-based cationic surfactant was examined as a stabilizer in the “wet chemistry” synthesis of silver and gold...
A new [1,3]thiazolo[3,2-b][1,2,4]triazol-7-ium-based cationic surfactant was examined as a stabilizer in the “wet chemistry” synthesis of silver and gold...
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SubjectTerms Cations
Chemical synthesis
Chemistry and Materials Science
Density functional theory
Electronic structure
Gold
Infrared analysis
Infrared spectroscopy
Materials Science
Membrane Biology
Nanochemistry
Nanoparticles
Nanotechnology
Nanotechnology and Microengineering
NMR
Nuclear magnetic resonance
Original Article
Quantum chemistry
Silver
Silver nitrate
Stabilizers (agents)
Surfactants
Title New [1,3]thiazolo[3,2-b][1,2,4]triazol-7-ium cationic surfactant as a stabilizer of silver and gold nanoparticles
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