Mesoporous tertiary oxides via a novel amphiphilic approach

We report a facile biomimetic sol-gel synthesis using the sponge phase formed by the lipid monoolein as a structure-directing template, resulting in high phase purity, mesoporous dysprosium- and gadolinium titanates. The stability of monoolein in a 1,4-butanediol and water mixture complements the use of a simple sol-gel metal oxide synthesis route. By judicious control of the lipid/solvent concentration, the sponge phase of monoolein can be directly realised in the pyrochlore material, leading to a porous metal oxide network with an average pore diameter of 10 nm

Activation of carbon dioxide and carbon disulfide by a scandium N-heterocyclic carbene complex

A Sc NHC complex readily activates three equivalents of CO2 showing ‘Frustrated Lewis Pair’ type reactivity with each metal–carbene bond, but whilst CS2 is also activated by the labile carbenes, no metal involvement is observed. Graphical abstract: Activation of carbon dioxide and carbon disulfide by a scandium N-heterocyclic carbene comple

LJETOPIS KULTURNIH ZBIVANJA U SPLITU

Fischer-Tropsch synthesis (FTS) is commonly viewed as an alternative approach to the production of diesel fuels via sources independent of crude oil. The adaptability of the FTS process allows for the selective production of shorter chain C2 to C6 hydrocarbons and has the potential to be a legitimate source of useable chemical feedstocks with high value to the chemical manufacturing industry. Interestingly, although recognised as a poison in most catalytic systems, small amounts of sulfur in iron-based FTS catalysts has been demonstrated to promote catalyst reducibility and activity towards shorter chain hydrocarbons. However, it is not known what impact sulfur has on the formation of hydrocarbonaceous surface species that have been proposed to play a pivotal role in the mediation of reactants during iron FTS. Here we apply ambient pressure CO hydrogenation at 623 K on a selection of sulfur promoted iron FTS catalysts to investigate the effect of sulfur content on hydrocarbonaceous species formation. For the first time, we report the application of inelastic neutron scattering to quantify the presence of hydrocarbonaceous species under the presence of sulfur promotion. In combination with temperature programmed oxidation, X-ray diffraction, and Raman spectroscopy, we observe how low sulfur loadings (<700 ppm) perturb carbon and hydrogen retention levels. The results indicate that the presence and nature of the hydrocarbonaceous overlayer is sensitive to sulfur loading, with the reported loss in catalytic activity at high loadings correlating with the attenuation of hydrocarbonaceous surface species

High-Throughput Discovery of Hf Promotion on the Formation of Hcp Co and Fischer-Tropsch Activity

A proxy-based high-throughput experimental approach was used to explore the stability and activity of Co-based Fischer Tropsch Synthesis catalysts with different promoters on various supports. The protocol is based on the estimation by XRD of active phase, Co, particle size and relative amounts of crystalline phases, Co to support. Sequential libraries samples enabled exploration of four Co loadings with five different promoters on six support materials. Catalysts stable to aging in syngas, displaying minimal change of particle size or relative area, were evaluated for their activity under industrial conditions. This procedure identified SiC as support for stable catalysts and a combination of Ru and Hf to promote the formation hcp Co. Unsupported bulk samples of Co with appropriate amounts of Ru and Hf revealed that the formation of hcp Co is independent of the support. The hcp Co containing catalyst presented the highest catalytic activity and C5+ selectivity amongst the samples tested in this study confirming the effectiveness of the proxy-based high-throughput method.</jats:p

Role of SNX16 in the Dynamics of Tubulo-Cisternal Membrane Domains of Late Endosomes

In this paper, we report that the PX domain-containing protein SNX16, a member of the sorting nexin family, is associated with late endosome membranes. We find that SNX16 is selectively enriched on tubulo-cisternal elements of this membrane system, whose highly dynamic properties and formation depend on intact microtubules. By contrast, SNX16 was not found on vacuolar elements that typically contain LBPA, and thus presumably correspond to multivesicular endosomes. We conclude that SNX16, together with its partner phosphoinositide, define a highly dynamic subset of late endosomal membranes, supporting the notion that late endosomes are organized in distinct morphological and functional regions. Our data also indicate that SNX16 is involved in tubule formation and cholesterol transport as well as trafficking of the tetraspanin CD81, suggesting that the protein plays a role in the regulation of late endosome membrane dynamics

Using Parahydrogen Induced Polarization to Study Steps in the Hydroformylation Reaction.

A range of iridium complexes, Ir(η3-C3H5)(CO)(PR2R’)2 (1a-1e) [where 1a, PR2R’ = PPh3, 1b P(p-tol)3, 1c PMePh2, 1d PMe2Ph and 1e PMe3] were synthesized and their reactivity as stoichiometric hydroformylation precursors studied. Para-hydrogen assisted NMR spectroscopy detected the following intermediates: Ir(H)2(η3-C3H5)(CO)(PR2R’) (2a-e), Ir(H)2(η1-C3H5)(CO)(PR2R’)2 (4d-e), Ir(H)2(η1-C3H5)(CO)2(PR2R’) (10a-e), Ir(H)2(CO-C3H5)(CO)2(PR2R’) (11a-c), Ir(H)2(CO-C3H7)(CO)2(PR2R’) (12a-c) and Ir(H)2(CO-C3H5)(CO)(PR2R’)2 (13d-e). Some of these species exist as two geometric isomers according to their multinuclear NMR characteristics. The NMR studies suggest a role for the following 16 electron species in these reactions: Ir(η3-C3H5)(CO)(PR2R’), Ir(η1-C3H5)(CO)(PR2R’)2, Ir(η1-C3H5)(CO)2(PR2R’), Ir(CO-C3H5)(CO)2(PR2R’), Ir(CO-C3H7)(CO)2(PR2R’) and Ir(CO-C3H5)(CO)(PR2R’)2. Their role is linked to several 18 electron species in order to confirm the route by which hydroformylation and hydrogenation proceeds