Growth and magnetic characterization of Co nanoparticles obtained by femtosecond pulsed laser deposition.

We present a detailed study on the morphology and magnetic properties of Co nanostructures deposited onto oxidized Si substrates by femtosecond pulsed laser deposition. Generally, Co disks of nanometric dimensions are obtained just above the ablation threshold, with a size distribution characterized by an increasingly larger number of disks as their size diminishes, and with a maximum disk size that depends on the laser power density. In Au/Co/Au structures, in-plane magnetic anisotropy is observed in all cases, with no indication of superparamagnetism regardless of the amount of material or the laser power density. Magnetic force microscopy observations show coexistence of single-domain and vortex states for the magnetic domain structure of the disks. Superconducting quantum interference device magnetometry and x-ray magnetic circular dichroism measurements point to saturation magnetization values lower than the bulk, probably due to partial oxidation of the Co resulting from incomplete coverage by the Au capping layer.

Carola Milà i la felicitat de ser una dona : La teoria feminista de Maria Aurèlia Capmany en 'Feliçment, jo sóc una dona'

Aquest treball presenta una anàlisi textual de l'obra de Maria Aurèlia Capmany 'Feliçment, jo sóc una dona'. D'una banda, a través d'una breu presentació de l'autora fins al moment de la publicació de l'obra i, d'una altra, d'una síntesi del feminisme a Catalunya, l'autora del treball ens apropa a les teories feministes que Capmany aboca en la seva novel·la, fet que representa un punt d'inflació en la seva trajectòria novel·lística. L'anàlisi textual ens permet apropar-nos al concepte d'identitat femenina i a la seva construcció, així com relacionar-lo amb les teories feministes més recents.

La trajectòria de Pere Farrés com a estudiós de Miquel Martí i Pol

Revisem la llarga trajectòria d’estudi i de difusió de l’obra de Miquel Martí i Pol que Pere Farrés Arderiu (1948-2008) va portar a terme. Fou el primer que n’oferí una lectura acadèmica i és considerat l’estudiós que més profundament coneixia la poesia martipoliana. A més, aportem nova informació sobre els orígens de la relació personal i la coneixença literària de tots dos, i destaquem de la seva producció la varietat de gèneres, fent èmfasi en les antologies que permeten la síntesi biobibliogràfica del poeta.

Total synthesis of (-)-isoavenaciolide

An enantioselective approach to (-)-isoavenaciolide was achieved starting from 1- undecyn-3-ol. The synthesis relied upon the preparation of a chiral 4-silyloxy-2-alkenylborane by hydroboration of a protected 2,3-allenol and subsequent stereoselective addition to 2- thiophenecarboxaldehyde

Protected maleimide building blocks for the decoration of peptides, peptoids and peptide nucleic acids

Monomers allowing for the introduction of [2,5-dimethylfuran]-protected maleimides into polyamides such as peptides, peptide nucleic acids, and peptoids were prepared, as well as the corresponding oligomers. Suitable maleimide deprotection conditions were established in each case. The stability of the adducts generated by Michael-type maleimide-thiol reaction and Diels-Alder cycloaddition to maleimide deprotection conditions was exploited to prepare a variety of conjugates from peptide and PNA scaffolds incorporating one free and one protected maleimide. The target molecules were synthesized by using two subsequent maleimide-involving click reactions separated by a maleimide deprotection step. Carrying out maleimide deprotection and conjugation simultaneously gave better results than performing the two reactions subsequently.

Més de tres segles d"història: les exploracions florístiques al Cadí-Moixeró i muntanyes veïnes.

El 2003 es va publicar el catàleg de plantes vasculars del Parc del Cadí-Moixeró i les serres veïnes; poc després un de nosaltres en va presentar una síntesi en el número 3 d"aquesta revista. Al·ludíem aleshores a l"important bagatge tant d"exploracions científiques com de dades sobre la flora del territori existents en el moment de redactar el catàleg; de fet, gairebé tots els botànics catalans, i molts de francesos i d"espanyols, hi han passat en algun moment i han contribuït al coneixement de la seva flora.

Unsaturated Oxazolopiperidone Lactams: an Unexpected Domino-type Double Conjugate Additioncyclization Process

Reactions of 2-acetylindole enolate with unsaturated oxazolopiperidones 3, 4 and 10 unexpectedly gives pentacyclic dilactams 6, 7 and 11, respectively, resulting from a domino-type process involving two successive conjugate additions and a final cyclization.

Preparation of penta-azole containing cyclopeptides: challenges in macrocyclization

Herein is described the synthesis of several analogs of the natural product IB-01211 from concatenated azoles, via a biomimetic pathway based on cyclization-oxidation of serine containing peptides combined with the Hantzsch synthesis. The macrocyclization of rigid peptide compounds 1 and 2 to give IB-01211 and its epimer 12b was explored, and the results are compared here to those previously obtained for the macrocyclization of more flexible structures in the syntheses of YM-216391, telomestatin, and IB-01211. Lastly, the preliminary results of anti-tumor activity screening of the synthesized analogs are discussed.

Total synthesis and antiproliferative activity screening of (±)-aplicyanins A, B and E and related analogs

The first total synthesis of the indole alkaloids ()-aplicyanins A, B and E, plus seventeen analogs, all in racemic form is reported. Modifications to the parent compound included changing the number of bromine substituents on the indole, the groups on the indole nitrogen (H, Me or OMe), and/or the oxidation level of the heterocyclic core tetrahydropyrimidine. Each compound was screened against three human tumor cell lines, and fourteen of the newly synthesized compounds showed considerable cytotoxicity. The assay results were used to establish structure-activity relationships. These results suggest that the acetyl group moiety on the imine nitrogen, and the bromine at position 5 of the indole, are both critical to activity.

Synthesis and antitumor activity of mechercharmycin A analogues

Several analogs of the cytotoxic thiopeptide IB-01211 or Mechercharmycin A (1) have been synthetized. The cytotoxicity of 1 and the synthetized analogs was evaluated against a panel of three human tumor cell lines. Thiopeptide 1 and the most active derivatives, 2 and 3c, were chosen for further studies like effects on cell cycle progression and induction of apoptosis. Interestingly, the inhibition of cell division and activation of a programmed cell death by apoptosis was detected.

Arduino Tricorder : Aplicació Android per a la supervisió, control i adquisició de dades d'una placa Arduino

Aplicació Android per a la supervisió, control i adquisició de dades d'una placa Arduino que disposi de comuninació Ethernet i/o Wi-Fi. Creació d'interfícies dinàmiques amb diferents modalitats d'interacció: tàctil, reconeixement de veu i síntesi de veu.

Actualidad de la Idea de una universidad de J. H. Newman

A mitjans de segle XIX, John Henry Newman va rebre l'encàrrec d'organitzar i dirigir una nova universitat a Dublin. Com a síntesi de les reflexions que van acompanyar aquell projecte, va publicar un escrit intitulat Idea of a University que encara avui dia ofereix nombrosos elements per a la reflexió de tots aquells que en formem part de la comunitat universitària. Els trets distintius de la universitat en què Newman hi pensa són: una vocació humil de servei que es concreta en la formació de persones, no tant de gentlemen o elits socials; primacia de l'educació de la intel·ligència especulativa, sense subordinar-la a l'educació moral ni a la formació tècnica; un lloc d'ensenyament del saber universal -deixant per altres institucions l'activitat de pura investigació- i de contacte viu entre les diferents especialitats -és bàsic l'intercanvi continu d'experiències entre docents i alumnes d'estudis diferents-; una acció tutorial que permeti descobrir en cada alumne els seus talents i les seves aptituds particulars; una producció o 'transferència de coneixement' vinculada a la vàlua real de l'activitat intel·lectual -qui publica ho fa perquè realment té quelcom a dir-. Com a rerefons d'aquestes propostes, Newman posa l'accent en la necessitat que la universitat sigui un ambient on es confia pregonament en la possibilitat d'accedir a un coneixement veritable de la realitat. Més que mai en un món intel·lectual que ja a mitjans segle XIX començava a trontollar sota el pes del nihilisme i l'escepticisme, Newman reivindica el valor de la veritat com a fi últim de tota vida universitària.

Membrane interaction of a new synthetic antimicrobial lipopetide sp-85 with broad spectrum activity

Antimicrobial peptides offer a new class of therapeutic agents to which bacteria may not be able todevelop genetic resistance, since their main activity is in the lipid component of the bacterial cell mem-brane. We have developed a series of synthetic cationic cyclic lipopeptides based on natural polymyxin,and in this work we explore the interaction of sp-85, an analog that contains a C12 fatty acid at theN-terminus and two residues of arginine. This analog has been selected from its broad spectrum antibac-terial activity in the micromolar range, and it has a disruptive action on the cytoplasmic membrane ofbacteria, as demonstrated by TEM. In order to obtain information on the interaction of this analog withmembrane lipids, we have obtained thermodynamic parameters from mixed monolayers prepared withPOPG and POPE/POPG (molar ratio 6:4), as models of Gram positive and Gram negative bacteria, respec-tively. LangmuirBlodgett films have been extracted on glass plates and observed by confocal microscopy,and images are consistent with a strong destabilizing effect on the membrane organization induced bysp-85. The effect of sp-85 on the membrane is confirmed with unilamelar lipid vesicles of the same com-position, where biophysical experiments based on fluorescence are indicative of membrane fusion andpermeabilization starting at very low concentrations of peptide and only if anionic lipids are present.Overall, results described here provide strong evidence that the mode of action of sp-85 is the alterationof the bacterial membrane permeability barrier.

The synthesis of 1,2,3,6,6a,7-hexahydro-7-methyl-5-imino-1H-pyrrolo[1,2-c]imidazolo[5,4-b]indole

N-3-(1-Methylindol-3-yl)propan-N-(2,2,2-trichloroethoxysulfonyl)guanidine was synthesized from 3-formyl-1-methylindole in six steps and subjected to conditions intended to convert the side-chain into a 2-iminotetrahydropyrimidine- containing product, of relevance to a possible synthesis of the aplicyanins. An alternative reaction course was observed, resulting in the formation of a new tetracyclic system.

Selenomethionine incorporation into amyloid sequences regulates fibrillogenesis and toxicity.

The capacity of a polypeptide chain to engage in an amyloid formation process and cause a conformational disease is contained in its sequence. Some of the sequences undergoing fibrillation contain critical methionine (Met) residues which in vivo can be synthetically substituted by selenomethionine (SeM) and alter their properties.