L p Regularity and partial Hölder continuity for solutions of second order parabolic systems with strictly controlled growth

Sunto Si dimostra innanzitutto la regolarità L^p-globale, 2 < p < p₀, delle derivate spaziali D_iu delle soluzioni di un problema di Cauchy-Dirichlet per sistemi parabolici lineari del II ordine definiti in un cilindro Q=×(0,T) Rⁿ×R_t, con dati al bordo nulli e coefficienti L. Questo risultato generalizza quello di [6]. Se ne deduce un risultato L^p-locale, 2

0, per le derivate spaziali D_iu di soluzioni di un sistema parabolico quasi-lineare del II ordine con andamenti strettamente controllati. Ne consegue che, sotto opportune ipotesi, le soluzioni in Q di un sistema parabolico quasi-lineare del II ordine con andamenti strettamente controllati, sono parzialmente hölderiane in Q nel senso che esiste un cilindro Q₀ Q, chiuso in Q e di misura di Hausdorff n-dimensionale 0, tal e che la soluzione u è hölderiana in QQ₀. Questo risultato generalizza quello di [8].     

Potential energy surface and rovibrational states of the ground Ar-HI complex

A potential energy surface for the ground electronic state of the Ar-HI van der Waals complex is calculated at the coupled-cluster with single and double excitations and a noniterative perturbation treatment of triple excitations [CCSD(T)] level of theory. Calculations are performed using for the iodine atom a correlation consistent triple-zeta valence basis set in conjunction with large-core Stuttgart-Dresden-Bonn relativistic pseudopotential, whereas specific augmented correlation consistent basis sets are employed for the H and Ar atoms supplemented with an additional set of bond functions. In agreement with previous studies, the equilibrium structure is found to be linear Ar-I-H, with a well depth of 205.38 cm(-1). Another two secondary minima are also predicted at a linear and bent Ar-H-I configurations with well depths of 153.57 and 151.57 cm(-1), respectively. The parametrized CCSD(T) potential is used to calculate rovibrational bound states of Ar-HI/Ar-DI complexes, and the vibrationally averaged structures of the different isomers are determined. Spectroscopic constants are also computed from the CCSD(T) surface and their comparison with available experimental data demonstrates the quality of the present surface in the corresponding configuration regions.     

Gadolinium‐Decorated Silica Microspheres as Redox‐Responsive MRI Probes for Applications in Cell Therapy Follow‐Up

The redox microenvironment within a cell graft can be considered as an indicator to assess whether the graft is metabolically active or hypoxic. We present a redox‐responsive MRI probe based on porous silica microparticles whose surface has been decorated with a Gd‐chelate through a disulphide bridge. Such microparticles are designed to be interspersed with therapeutic cells within a biocompatible hydrogel. The onset of reducing conditions within the hydrogel is paralleled by an increased clearance of Gd, that can be detected by MRI.     

A transmission problem on a polygonal partition: regularity and shape differentiability

We consider a transmission problem on a polygonal partition for the two-dimensional conductivity equation. For suitable classes of partitions we establish the exact behaviour of the gradient of solutions in a neighbourhood of the vertexes of the partition. This allows to prove shape differentiability of solutions and to establish an explicit formula for the shape derivative.     

Expanding the Scope of Arylsulfonylacetylenes as Alkynylating Reagents and Mechanistic Insights in the Formation of Csp2?Csp and Csp3?Csp Bonds from Organolithiums

We describe the unexpected behavior of the arylsulfonylacetylenes, which suffer an “anti‐Michael” addition of organolithiums producing their alkynylation under very mild conditions. The broad scope, excellent yields, and simplicity of the experimental procedure are the main features of this methodology. A rational explanation of all these results can be achieved by theoretical calculations, which suggest that the association of the organolithiums to the electrophile is a previous step of their intramolecular attack and is responsible for the unexpected “anti‐Michael” reactions observed for substituted sulfonylacetylenes.