01958nas a2200229   4500008004100000022001400041245011700055210006900172260009200241300001400333490000600347520110700353653002301460653002001483653001601503653000801519100002001527700002001547700001901567700001801586856012401604       2006                        eng d  a1533-488000aDirect synthesis of nanocrystalline silver from the reaction between silver carboxylates and n-trioctylphosphine0 aDirect synthesis of nanocrystalline silver from the reaction bet  a26650 THE OLD RD, STE 208, VALENCIA, CA 91381-0751 USAbAMER SCIENTIFIC PUBLISHERScJUL  a2095-21020 v63 a<p>Neat n-Trioctylphosphine (TOP) has been used for the first ever time for reduction of silver nitrate and silver carboxylates (citrate, oleate, and myristate) under mild thermal reaction conditions. UV-visible absorption measurements of re-dispersible silver particles that were obtained by reduction of silver myristrate (product-IV) and silver nitrate (product-I) showed surface plasmon resonance absorption peak at 400 nm. The powder XRD pattern of fcc zero-valent silver resulted in diameters in the range of about 25-30 nm. TEM analysis showed particle diameter similar to that was observed by the XRD. FTIR spectroscopy revealed that the organics from the carboxylate group are retained by the nano-particles in case of product-IV however, presence of TOP is observed in product-I. It is found that when silver nitrate is reduced by TOP, spherical silver nano-particles with poor redispersity are formed but extended heating results in formation of long silver rods of micrometer size however, the re-dispersible nano-particles are easily formed when silver carboxylates are reduced by TOP.</p>10aChemical synthesis10aNanocrystalline10anoble metal10aXRD1 aCharan, Shobhit1 aSingh, Narendra1 aKhanna, P., K.1 aPatil, K., R.  uhttps://library.ncl.res.in/content/direct-synthesis-nanocrystalline-silver-reaction-between-silver-carboxylates-and-n-002131nas a2200241   4500008004100000022001400041245010800055210006900163260007300232300001400305490000700319520127900326653002301605653001801628653001801646653000801664100002001672700002001692700001801712700002201730700001901752856011801771       2006                        eng d  a0167-577X00aUnusual formation of nano-particles of CdO and Cd(OH)(2) from the reaction of dimethyl cadmium with DMF0 aUnusual formation of nanoparticles of CdO and CdOH2 from the rea  aPO BOX 211, 1000 AE AMSTERDAM, NETHERLANDSbELSEVIER SCIENCE BVcDEC  a3492-34980 v603 a<p>This paper presents generation of CdO and Cd(OH)(2) nano-particles from Dimethyl Cadmium in DMF. The CdO nano-particles were obtained instead of CdSe, even when the reaction was done in presence of 1,2,3-selenadiazole (the source of selenium) with Me2Cd in DMF (product-I). The direct reaction of Me2Cd in DMF also leads to formation of CdO (product-II). However, Cd(OH)(2) nano-particles were obtained when Me2Cd was refluxed in DMF for a few hours followed by reaction of H2S gas (product-III). The formation of Cd(OH)(2) was also established via decomposition Of Me2Cd:Et2O adduct (product-IV). Nano-particles of CdO and Cd(OH)(2) (product-I to product-IV) were characterized by X-ray powder diffraction (XRD), TEM and SEM/EDS measurements, FTIR, thermal analysis (TGA) and XPS analysis. The particle size of all the products as calculated by XRD patterns were in the range of about 20 nm. TEM images showed that the products are agglomerated clusters with the particles in the nano-meter regime. The synthesis however, is understood to be unusual as the reactions with selenium source and sulfur source should have generated the CdSe and CdS however, the end products were always found to be the product-I to product-IV (c) 2006 Elsevier B.V. All rights reserved.</p>10aChemical synthesis10aNanoparticles10aSemiconductor10aXRD1 aSingh, Narendra1 aCharan, Shobhit1 aPatil, K., R.1 aViswanath, A., K.1 aKhanna, P., K.  uhttps://library.ncl.res.in/content/unusual-formation-nano-particles-cdo-and-cdoh2-reaction-dimethyl-cadmium-dmf-0