Synthesis and characterization of silver nanoparticles from (bis) alkylamine silver carboxylate precursors

A comparative study of amine and silver carboxylate adducts [R1COOAg-2(R2NH2)] (R-1 = 1, 7, 11; R-2 = 8, 12) as a key intermediate in NPs synthesis is carried out via differential scanning calorimetry, solidstate FT-infrared spectroscopy, C-13 CPMAS NMR, powder X-ray diffraction and X-ray photoelectron spectroscopy, and various solution NMR spectroscopies (H-1 and C-13 NMR, pulsed field gradient spin-echo NMR, and ROESY). It is proposed that carboxyl moieties in the presence of amine ligands are bound to silver ions via chelating bidentate type of coordination as opposed to bridging bidentate coordination of pure silver carboxylates resulting from the formation of dimeric units. All complexes are packed as lamellar bilayer structures. Silver carboxylate/amine complexes show one first-order melting transition. The evidence presented in this study shows that phase behavior of monovalent metal carboxylates are controlled, mainly, by head group bonding. In solution, insoluble silver salt is stabilized by amine molecules which exist in dynamic equilibrium. Using (bis) amine-silver carboxylate complex as precursor, silver nanoparticles were fabricated. During hightemperature thermolysis, the (bis) amine-carboxylate adduct decomposes to produce silver nanoparticles of small size. NPs are stabilized by strongly interacting carboxylate and trace amounts of amine derived from the silver precursor interacting with carboxylic acid. A corresponding aliphatic amide obtained from silver precursor at high-temperature reaction conditions is not taking part in the stabilization. Combining NMR techniques with FTIR, it was possible to follow an original stabilization mechanism.