ABSTRACT
Solvothermal reaction of a mixture of Sn, Mn, and Te at 200 degrees C using teta as the solvent yields a novel inorganic-organic hybrid solid [Mn(teta)(en)].[Mn(teta)][Mn(SnTe4)2.Mn(teta)] (teta=triethylenetetramine and en=ethylenediamine; 1), which has a homochiral single-stranded helical structure. The material is a semiconductor with a band gap of 0.88 eV and shows paramagnetic behavior between 2 and 300 K.
Subject(s)
Metals/chemistry , Tellurium/chemistry , Models, Molecular , Molecular Conformation , Spectrophotometry , Stereoisomerism , TemperatureABSTRACT
A high-temperature solution-phase hydrolysis approach has been developed for the synthesis of colloidal magnetite nanocrystals with well-controlled size and size distribution, high crystallinity, and high water solubility. The synthesis was accomplished by the hydrolysis and reduction of iron(III) cations in diethylene glycol with a rapidly injected solution of sodium hydroxide at an elevated temperature. The high reaction temperature allows for control over size and size distribution and yields highly crystalline products. The superior water solubility is achieved by using a polyelectrolyte, that is, poly(acrylic acid) as the capping agent, the carboxylate groups of which partially bind to the nanocrystal surface and partially extend into the surrounding water. The direct synthesis of water-soluble nanocrystals eliminates the need for additional surface modification steps which are usually required for treating hydrophobic nanocrystals produced in nonpolar solvents through the widely recognized pyrolysis route. The abundant carboxylate groups on the nanocrystal surface allow further modifications, such as bioconjugation, as demonstrated by linking cysteamine to the particle surface. The monodisperse, highly water-soluble, superparamagnetic, and biocompatible magnetite nanocrystals should find immediate important biomedical applications.
