A flexible one-pot route to metal/metal oxide nanocomposites

We report a one-pot route to Au/CeO2 nanocomposites. A readily-available biopolymer, sodium alginate, is exploited for controlled formation and stabilisation of gold nanoparticles followed by in situ growth of a sponge-like network of CeO2 nanoparticles. The flexible nature of this method as a general route to mixed metal/metal oxide nanocomposites is also demonstrated

The effects on grain quality traits of a grain serpin protein and the VPM 1 segment in southern Australian wheat breeding

Trabalho final do 6º ano médico com vista à atribuição do Grau de Mestre no âmbito do ciclo de estudos de mestrado integrado em medicina da Faculdade de Medicina de Coimbra.Introdução: Estudos prévios estabeleceram que até 12% dos doentes com enfarte agudo do miocárdio não demonstravam lesão coronária aparente ao exame angiográfico. Contudo, existe muito pouca informação disponível acerca deste fenómeno em enfartes agudos do miocárdio sem elevação do segmento ST. O objectivo deste estudo foi avaliar uma população de doentes com esse diagnóstico sujeitos a angiografia coronária, analisando e comparando as características clínicas e os prognósticos entre os que não revelaram lesão coronária aparente e os que apresentavam doença coronária epicárdica. Métodos: O nosso estudo avaliou 270 doentes com enfarte agudo do miocárdio sem elevação do segmento ST que foram sujeitos a angiografia coronária nas primeiras 72 horas de enfarte. Foram valorizadas as características demográficas, clínicas, parâmetros analíticos, achados electrocardiográficos, fracção de ejecção ventricular esquerda, duração do internamento e prognóstico.Previous studies established that up to 12% of patients with acute myocardial infarction did not present coronary atherosclerotic disease demonstrable with angiographic exam. However, little information is available about this phenomenon in acute non-STelevation myocardial infarction. We examined a population of patients with this diagnosis who had undergone coronary angiography, assessing and comparing the clinical characteristics and prognosis between the subset of patients with angiographically normal coronary arteries and the subset of patients with coronary disease

Doped-carbon electrocatalysts with trimodal porosity from a homogeneous polypeptide gel

One of the biggest challenges for materials science is to design facile routes to structurally complex materials, which is particularly important for global applications such as fuel cells. Doped nanostructured carbons are targeted as noble metal-free electrocatalysts for this purpose. Their intended widespread use, however, necessitates simple and robust preparation methods that do not compromise on material performance. Here, we demonstrate a versatile one-pot synthesis of nitrogen-doped carbons that exploits the templating ability of biological polymers. Starting with just metal nitrates and gelatin, multiphase C/Fe3C/MgO nanomaterials are formed, which are then etched to produce active carbon electrocatalysts with accessible trimodal porosity. These show remarkable performance in the oxygen reduction reaction – a key process in proton exchange membrane fuel cells. The activity is comparable to commercial platinum catalysts and shows improved stability with reduced crossover effects. This simple method offers a new route to widely applicable porous multicomponent nanocomposites

Flourescent liquid pyrene derivative-in-water mircoemulsions

A fluorescent liquid pyrene derivative with a high fluorescence quantum yield (65%) in the bulk state is reported. With this as the sole oil phase, stable luminescent oil-in-water microemulsions have been prepared. Increasing the loading of liquid pyrene swells the droplets, as detected by small-angle neutron scattering. These larger droplets have a greater proportion of pyrene excimer emission contribution in their photoluminescence spectra, which leads to a red shift in the chromaticity of the emission

Non-uniform Photoinduced Unfolding of Supramolecular Polymers Leading to Topological Block Nanofibers

Synthesis of one-dimensional nanofibers with distinct topological (higher-order structural) domains in the same main chain is one of the challenging topics in modern supramolecular polymer chemistry. Non-uniform structural transformation of supramolecular polymer chains by external stimuli may enable preparation of such nanofibers. To demonstrate feasibility of this post-polymerization strategy, we prepared a photoresponsive helically folded supramolecular polymers from a barbiturate monomer containing an azobenzene-embedded rigid π-conjugated scaffold. In contrast to previous helically folded supramolecular polymers composed of a more flexible azobenzene monomer, UV-light induced unfolding of the newly prepared helically folded supramolecular polymers occurred nonuniformly, affording topological block copolymers consisting of folded and unfolded domains. The formation of such blocky copolymers indicates that the photoinduced unfolding of the helically folded structures initiates from relatively flexible parts such as termini or defects. Spontaneous refolding of the unfolded domains was observed after visible-light irradiation followed by aging to restore fully folded structures

The aggregation of an alkyl-C₆₀ derivative as a function of concentration, temperature and solvent type

Contrast-variation SANS, SAXS, NMR and ITC measurements show that molecule1associates into micelles with tunable size based on the solution parameters.</p

Light-induced unfolding and refolding of supramolecular polymer nanofibres.

Unlike classical covalent polymers, one-dimensionally (1D) elongated supramolecular polymers (SPs) can be encoded with high degrees of internal order by the cooperative aggregation of molecular subunits, which endows these SPs with extraordinary properties and functions. However, this internal order has not yet been exploited to generate and dynamically control well-defined higher-order (secondary) conformations of the SP backbone, which may induce functionality that is comparable to protein folding/unfolding. Herein, we report light-induced conformational changes of SPs based on the 1D exotic stacking of hydrogen-bonded azobenzene hexamers. The stacking causes a unique internal order that leads to spontaneous curvature, which allows accessing conformations that range from randomly folded to helically folded coils. The reversible photoisomerization of the azobenzene moiety destroys or recovers the curvature of the main chain, which demonstrates external control over the SP conformation that may ultimately lead to biological functions

Directed assembly of optoelectronically active alkyl-<i>π</i>-conjugated molecules by adding <i>n</i>-alkanes or <i>π</i>-conjugated species

Supramolecular assembly can yield ordered structures by taking advantage of the cumulative effect of multiple non-covalent interactions between adjacent molecules. The thermodynamic origin of many self-assembled structures in water is the balance between the hydrophilic and hydrophobic segments of the molecule. Here, we show that this approach can be generalized to use solvophobic and solvophilic segments of fully hydrophobic alkylated fullerene molecules. Addition of n-alkanes results in their assembly--due to the antipathy of C60 towards n-alkanes--into micelles and hexagonally packed gel-fibres containing insulated C60 nanowires. The addition of pristine C60 instead directs the assembly into lamellar mesophases by increasing the proportion of π-conjugated material in the mixture. The assembled structures contain a large fraction of optoelectronically active material and exhibit comparably high photoconductivities. This method is shown to be applicable to several alkyl-π-conjugated molecules, and can be used to construct organized functional materials with π-conjugated sections