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Erschienen in: Colloid and Polymer Science 4/2017

21.02.2017 | Original Contribution

Preparation and optical properties of colloidal Ag0 nanoclusters from reduction of solution ionomer Ag-carboxylate ionic aggregates activated by swelling of covalently attached chain segments

verfasst von: Bofeng Li, Tao Hu, Nian Ma, Zhen Hu, Xinghou Gong, Chonggang Wu, Masanori Hara

Erschienen in: Colloid and Polymer Science | Ausgabe 4/2017

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Abstract

Small colloidal Ag0 nanoclusters successfully were prepared from solution reaction of CH3COOAg with a copolymer acid, poly(methyl methacrylate-ran-methacrylic acid) (MMA–MAA), in a methanol-containing solvent at room temperature in the dark in the absence of a typical chemical reductant. Tentatively mechanistically, slow PMMA-ionomerisation of the Ag+ ions produces intramolecular –COO–Ag+ aggregate cross-links in the solution, which, upon swelling of the chain segments covalently bound to them, are activated by the resultant elastic forces to dissociate instantaneously at the O–Ag coordination bonds to give bare (i.e. uncoordinated), highly oxidative Ag+ ions, which are subject to reduction by the active α-H atoms of the solvent methanol to make Ag0 nanoclusters supported by the re-formed MMA–MAA; the MMA–MAA acid-copolymer, without itself undergoing any permanent chemical change, serves as a mechanical-activator or, say, catalyst for the mechanochemical reduction of CH3COOAg. This novel, facile approach may universally be extended to fabricate other transition-metal nanoclusters deposited in diverse polymeric matrices.

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Metadaten
Titel
Preparation and optical properties of colloidal Ag0 nanoclusters from reduction of solution ionomer Ag-carboxylate ionic aggregates activated by swelling of covalently attached chain segments
verfasst von
Bofeng Li
Tao Hu
Nian Ma
Zhen Hu
Xinghou Gong
Chonggang Wu
Masanori Hara
Publikationsdatum
21.02.2017
Verlag
Springer Berlin Heidelberg
Erschienen in
Colloid and Polymer Science / Ausgabe 4/2017
Print ISSN: 0303-402X
Elektronische ISSN: 1435-1536
DOI
https://doi.org/10.1007/s00396-017-4033-9

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