Hollow nanostructures of platinum with controllable dimensions can be synthesized by templating against selenium nanowires and colloids

Hollow nanostructures of platinum have been synthesized by reducing PtCl2 with alcohol in the presence of selenium nanowires or colloids. The Se template could be removed by soaking the resultant Se@Pt nanostructures in hydrazine or by heating them to 200-250 degrees C. The size and wall thickness of the polycrystalline hollow nanostructures could be controlled by varying the template, reaction time, and the concentration of PtCl2.     

Synthesis of lanthanide and lanthanide-silicate aerogels

In this paper we report on the preparation of mixed lanthanide-silicate and pure lanthanide aerogels from the chlorides of erbium, praseodymium, and neodymium. A two-step sol-gel method is described for preparing the mixed aerogels, using a sub-stoichiometric amount of water in the first step to prepare a partially condensed silica-lanthanide precursor. The pure lanthanide aerogels are prepared directly from the chlorides using propylene oxide as a scavenger for reaction generated hydrochloric acid. The aerogel microstructures vary from colloidal for the pure lanthanide and high weight percent lanthanide-silicate aerogels to polymeric for the low weight percent lanthanide-silicate aerogels. This change in microstructure is also indicated by the BET analyses, which show that the surface areas decrease with increasing lanthanide concentrations. In general, we measured reductions of lanthanide contents during the supercritical drying step due to insufficient linking and subsequent washing out of the lanthanides from the gels. Also, the retention efficiency for the lanthanide improves with higher silica concentrations, making quantitative doping by this method practical only for the lower lanthanide concentrations.     

Metal ion promoted transesterifications of carboxylate esters. A structure/activity study of the efficacy of Zn2+ and La3+ to catalyze the methanolysis of some aryl and aliphatic esters

The methanolysis of various aryl and aliphatic carboxylate esters promoted by methoxide, 1,5,9-triazacyclododecane : Zn2+(-OCH3) and La3+(-OCH3), were studied and the derived rate constants (kOCH3, kcat3:Zn(OCH3) and kcatLa(OCH3)) correlated in various ways. The metal ion catalyzed reactions are very much faster than the background reactions in some cases reaching up to 7 x 10(6)-fold acceleration when present at concentrations of 5 mmol dm(-3). The data for both metals exhibit non-linear Bronsted correlations with the pKa of the leaving group which are analyzed in terms of a change in rate limiting step from formation to breakdown of a metal-coordinated tetrahedral intermediate as the pKa increases above values of approximately 14.7. Plots of the log kOCH3 reaction vs. the log kcat values for each metal ion indicate low sensitivity for aryl esters and a higher sensitivity for the aliphatic esters. A mechanistic rationale for the observations is presented.     

Biomimetic studies of terminal oxidases: trisimidazole picket metalloporphyrins

Three biomimetic models for the binuclear Fe/Cu (heme/trisimidazole) active site of terminal oxidases, such as cytochrome c oxidase and related enzymes, have been prepared. Based upon a tetrakis(aminophenyl)porphyrin core, these models possess a single covalently linked imidazole-bearing tail on one side of the porphyrin and three imidazole "pickets" on the opposite side of the porphyrin ring. Three different imidazole picket motifs are characterized in free base, Fe, Zn, Fe/Cu, and Zn/Cu forms. A combination of NMR, EPR, and IR demonstrates that, for the N-methylimidazole systems studied, the distal Cu is bound within the trisimidazole environment in the reduced (Cu(I)) and oxidized (Cu(II)) forms. The imidazole picket substitution pattern and state of metalation have significant influence on the interaction of these compounds with CO. For imidazole picket systems containing NH groups, intramolecular H bonds compete with Cu(I) coordination of the N donors.     

On the nature of pulsars

The paper contains a relatively non-technical summary of some recent work by the author and Jeremy Butterfield. The goal is to find a way of assigning meaningful truth values to propositions in quantum theory: something that is not possible in the normal, instrumentalist interpretation. The key mathematical tool is presheaf theory where multi-valued, contextual truth values arise naturally. We show how this can be applied to quantum theory, with the ‘contexts’ chosen to be Boolean subalgebras of the set of all projection operators.