9 research outputs found
Supersymmetry and Polytopes
We make an imaginative comparison between the Minimal Supersymmetric Standard
Model and the 24-cell polytope in four dimensions, the Octacube.Comment: Presented to the Workshop on Geometry and Physics: Supersymmetry.
Bilbao, Spain. May 200
Gauge theory in dimension
We first review the notion of a -manifold, defined in terms of a
principal ("gauge") bundle over a -dimensional manifold, before
discussing their relation to supergravity. In a second thread, we focus on
associative submanifolds and present their deformation theory. In particular,
we elaborate on a deformation problem with coassociative boundary condition.
Its space of infinitesimal deformations can be identified with the solution
space of an elliptic equation whose index is given by a topological formula.Comment: 15 page
The Classification of Highly Supersymmetric Supergravity Solutions
The spinorial geometry method is an effective method for constructing
systematic classifications of supersymmetric supergravity solutions. Recent
work on analysing highly supersymmetric solutions in type IIB supergravity
using this method is reviewed [arXiv:hep-th/0606049, arXiv:0710.1829]. It is
shown that all supersymmetric solutions of IIB supergravity with more than 28
Killing spinors are locally maximally supersymmetric.Comment: 23 pages, latex. To appear in the proceedings of the Special Metrics
and Supersymmetry conference at Universidad del Pais Vasco, May 2008.
References correcte
Graded geometry and Poisson reduction
The main result of [2] extends the Marsden-Ratiu reduction theorem [4] in Poisson geometry, and is proven by means of graded geometry. In this note we provide the background material about graded geometry necessary for the proof in [2]. Further, we provide an alternative algebraic proof for the main result. ©2009 American Institute of Physic
Mono‑, Bi‑, and Trinuclear Bis-Hydrated Mn<sup>2+</sup> Complexes as Potential MRI Contrast Agents
We report a series of ligands containing
pentadentate 6,6′-((methylazanediyl)bis(methylene))dipicolinic
acid binding units that form mono- (H<sub>2</sub>dpama), di- (<i>m</i>X(H<sub>2</sub>dpama)<sub>2</sub>), and trinuclear (<i>m</i>X(H<sub>2</sub>dpama)<sub>3</sub>) complexes with Mn<sup>2+</sup> containing two coordinated water molecules per metal ion,
which results in pentagonal bipyramidal coordination around the metal
ions. In contrast, the hexadentate ligand 6,6′-((ethane-1,2-diylbis(azanediyl))bis(methylene))dipicolinic
acid (H<sub>2</sub>bcpe) forms a complex with distorted octahedral
coordination around Mn<sup>2+</sup> that lacks coordinated water molecules.
The protonation constants of the ligands and the stability constants
of the Mn<sup>2+</sup>, Cu<sup>2+</sup>, and Zn<sup>2+</sup> complexes
were determined using potentiometric and spectrophotometric titrations
in 0.15 M NaCl. The pentadentate dpama<sup>2–</sup> ligand
and the di- and trinucleating mX(dpama)<sub>2</sub><sup>4–</sup> and mX(dpama)<sub>3</sub><sup>6–</sup> ligands provide metal
complexes with stabilities that are very similar to that of the complex
with the hexadentate ligand bcpe<sup>2–</sup>, with log β<sub>101</sub> values in the range 10.1–11.6. Cyclic voltammetry
experiments on aqueous solutions of the [Mn(bcpe)] complex reveal
a quasireversible system with a half-wave potential of +595 mV versus
Ag/AgCl. However, [Mn(dpama)] did not suffer oxidation in the range
0.0–1.0 V, revealing a higher resistance toward oxidation.
A detailed <sup>1</sup>H NMRD and <sup>17</sup>O NMR study provided
insight into the parameters that govern the relaxivity for these systems.
The exchange rate of the coordinated water molecules in [Mn(dpama)]
is relatively fast, <i>k</i><sub>ex</sub><sup>298</sup> = (3.06 ± 0.16) × 10<sup>8</sup> s<sup>–1</sup>. The trinuclear [mX(Mn(dpama)(H<sub>2</sub>O)<sub>2</sub>)<sub>3</sub>] complex was found to bind human
serum albumin with an association constant of 1286 ± 55 M<sup>–1</sup> and a relaxivity of the adduct of 45.2 ± 0.6
mM<sup>–1</sup> s<sup>–1</sup> at 310 K and 20 MHz
Stabilizing Divalent Europium in Aqueous Solution Using Size-Discrimination and Electrostatic Effects
We report two macrocyclic ligands
containing a 1,10-diaza-18-crown-6 fragment functionalized with either
two picolinamide pendant arms (bpa18c6) or one picolinamide and one
picolinate arm (ppa18c6<sup>–</sup>). The X-ray structure of
[La(ppa18c6)(H<sub>2</sub>O)]<sup>2+</sup> shows that the ligand binds
to the metal ion using the six donor atoms of the crown moiety and
the four donor atoms of the pendant arms, 11-coordination being completed
by the presence of a coordinated water molecule. The X-ray structure
of the [Sr(bpa18c6)(H<sub>2</sub>O)]<sup>2+</sup> was also investigated
due to the very similar ionic radii of Sr<sup>2+</sup> and Eu<sup>2+</sup>. The structure of this complex is very similar to that of
[La(ppa18c6)(H<sub>2</sub>O)]<sup>2+</sup>, with the metal ion being
11-coordinated. Potentiometric measurements were used to determine
the stability constants of the complexes formed with La<sup>3+</sup> and Eu<sup>3+</sup>. Both ligands present a very high selectivity
for the large La<sup>3+</sup> ion over the smaller Eu<sup>3+</sup>, with a size-discrimination ability that exceeds that of the analogous
ligand containing two picolinate pendant arms reported previously
(bp18c6<sup>2–</sup>). DFT calculations using the TPSSh functional
and the large-core pseudopotential approximation provided stability
trends in good agreement with the experimental values, indicating
that charge neutral ligands derived from 1,10-diaza-18-crown-6 enhance
the selectivity of the ligand for the large Ln<sup>3+</sup> ions.
Cyclic voltammetry measurements show that the stabilization of Eu<sup>2+</sup> by these ligands follows the sequence bp18c6<sup>2–</sup> < ppa18c6<sup>–</sup> < bpa18c6 with half-wave potentials
of −753 mV (bp18c6<sup>2–</sup>), −610 mV (ppa18c6<sup>–</sup>), and −453 mV (bpa18c6) versus Ag/AgCl. These
values reveal that the complex of bpa18c6 possesses higher stability
against oxidation than the aquated ion, for which an <i>E</i><sub>1/2</sub> value of −585 mV has been measured
Memorias I Congreso Internacional. Universidad, desarrollo y cooperación
La participación de la Universidad Politécnica Salesiana, representada por su Rector, en el III Congreso sobre Universidad, Cooperación y Desarrollo, en Madrid, abril de 2006, la publicación n. 8 de la revista Universitas dedicada al tema ¿Qué cooperación para qué desarrollo? y una experiencia generalizada tanto en Ecuador como en América latina de la urgente necesidad de repensar y replantear la Cooperación Internacional desde los Desarrollos Nacionales, fueron los tres precedentes principales para la organización del I Congreso sobre Uni-versidad, Desarrollo y Cooperación.
A la iniciativa de organizar dicho Congreso en Cuenca, con motivo de las celebraciones de los 450 años de fundación de la ciudad, junto con la Universidad Politécnica Salesiana, se unieron la Universidad de Cuenca, Universidad del Azuay, Universidad Particular Técnica de Loja, Universidad Santa María de Guayaquil y el Fondo Ecuatoriano Populorum Progressio FEPP. Todo el proyecto contó con el apoyo financiero del Municipio de Cuenca, del Consejo Provincial del Azuay, la Agencia Española de Cooperación Internacional, y de las Universidades participantes. Así mismo el Congreso se benefició del apoyo académico de la Universidad de Murcia.
Las tres Conferencias que enmarcaron el Congreso, coincidieron desde enfoques diferentes en una misma estimación de las relaciones entre Cooperación Internacional y Desarrollo Nacional. José de Souza, a partir de la problemática y experiencia de un desarrollo posible en América Latina, hizo un balance crítico no sólo de la Cooperación Internacional respecto de dicho desarrollo, sino también de las relaciones entre países desarrollados y subdesarrollados. Alfonso Moro, tomando como referencia principal las políticas y programas de la cooperación europea con América Latina, puso de manifiesto las relaciones de desigualdad y dependencia impuestas por dicha cooperación, las cuales condicionan y limitan las reales posibilidades de desarrollos autónomos y sostenidos en los países latinoamericanos
Extreme blazars under the eyes of MAGIC
Extreme high-frequency-peaked BL Lac objects (EHBLs) are the most energetic persistent sources in the universe. This contribution reports on long-term observing campaigns of tens of EHBLs that have been organized by the MAGIC collaboration to enlarge their population at VHE and understand the origin of their extreme properties. EHBLs are characterized by a spectral energy distribution (SED) featuring a synchrotron peak energy above 1 keV. Several EHBLs display a hard spectral index at very high energies (VHE; E > 100 GeV), suggesting a gamma-ray SED component peaking significantly above 1 TeV. Such extreme properties are challenging current standard emission and acceleration mechanisms. Recent studies have also unveiled intriguing disparities in the temporal characteristics of EHBLs. Some sources seem to display a persistent EHBL behaviour, while others belong to the EHBL family only temporarily. Here, we present recent results of the first hard-TeV EHBL catalog. The MAGIC observations are accompanied by an extensive multiwavelength coverage to obtain an optimal determination of the SED. This allow us to investigate leptonic and hadronic scenarios for the emission. We also present the recent detection of the EHBL RX J0812.0+0237 in the VHE band by MAGIC. Finally, we discuss a broad multiwavelength campaign on the BL Lac type object 1ES 2344+514, which showed intermittent EHBL characteristics in August 2016