Small, carboxymethyl-starch-stabilised zinc oxide nanoparticles with a defined shape, size and morphology were prepared in situ in water at relatively low reaction temperatures using soluble carboxymethyl starch (CMS) as a combined crystallising, stabilising and solubilising agent and triethanolamine as the reducing agent. Aqueous colloidal solutions of these CMS-stabilised ZnO nanoparticles were used to deposit a coating of ZnO nanoparticles on cellulose paper by a wet-chemistry, polyelectrolyte, layer-by-layer approach using water as the only solvent. Such cellulose paper samples, coated with these CMS-stabilised ZnO nanoparticles, show higher brightness and whiteness than that of blank reference paper and are more stable to UV-radiation than the paper reference as well as demonstrating good antibacterial activity against MRSA and A.
View Article and Find Full Text PDFThe synthesis of nanoparticles has experienced a huge development over the past 20 years. However, this development has remained relatively limited to a few classes of nanomaterials such as iron oxides, semi-conducting oxides, plasmonic nanoparticles (essentially Au) and quantum dots. In these cases, a physical chemistry approach and standard recipes allow a good control of the size and shape of the resulting nano-objects.
View Article and Find Full Text PDFThe reaction of the metal-organic precursor Fe[N(SiMe3)2]2 with H2 in the presence of a long-chain acid and a long-chain amine in various proportions produces monodisperse zerovalent iron nanoparticles. These Fe particles display magnetic properties that match those of bulk iron as evidenced by magnetic and Mössbauer measurements. The nanoparticles adopt a cubic shape with edges of 7 nanometers and are incorporated into extended crystalline superlattices containing nanocubes in close proximity and with their crystallographic axes aligned.
View Article and Find Full Text PDFCo and NiFe nanoparticles (2.7 to 3.3 nm mean diameter) of narrow size distribution have been obtained through the decomposition of organometallic precursors in organic solutions of long alkyl chain ligands, namely oleic acid and hexadecylamine.
View Article and Find Full Text PDFThe dinuclear (Fe(II), Gd(III)) complexes studied in this report derive from hexadentate Schiff base ligands abbreviated H(2)L(i)() (i = 1, 2, 3). H(2)L(1) = N,N'-bis(3-methoxysalicylidene)-1,3-diamino-2,2'-dimethyl-propane, H(2)L(2) = N,N'-bis(3-methoxysalicylidene)-1,2-diamino-2-methylpropane, and H(2)L(3) = N,N'-bis(3-methoxysalicylidene)-1,2-diaminoethane. The crystal and molecular structures of three complexes have been determined at 160 K.
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