A Journey from Thermally Tunable Synthesis to Spectroscopy of Phenylmethanimine in Gas Phase and Solution

Phenylmethanimine is an aromatic imine with a twofold relevance in chemistry: organic synthesis and astrochemistry. To tackle both aspects, a multidisciplinary strategy has been exploited and a new, easily accessible synthetic approach to generate stable imine-intermediates in the gas phase and in solution has been introduced. The combination of this formation pathway, based on the thermal decomposition of hydrobenzamide, with a state-of-the-art computational characterization of phenylmethanimine laid the foundation for its first laboratory observation by means of rotational electric resonance spectroscopy. Both E and Z isomers have been accurately characterized, thus providing a reliable basis to guide future astronomical observations. A further characterization has been carried out by nuclear magnetic resonance spectroscopy, showing the feasibility of this synthetic approach in solution. The temperature dependence as well as possible mechanisms of the thermolysis process have been examined.     

More on trees and Cohen reals

In this paper we analyse some questions concerning trees on κ, both for the countable and the uncountable case, and the connections with Cohen reals. In particular, we provide a proof for one of the implications left open in [6, Question 5.2] about the diagram for regularity properties.     

The Asymptotic Behaviour of the Fourier Transforms of Orthogonal Polynomials I: Mellin Transform Techniques

The Fourier transform of orthogonal polynomials with respect to their own orthogonality measure defines the family of Fourier–Bessel functions. We study the asymptotic behaviour of these functions and of their products, for large real values of the argument. By employing a Mellin analysis we construct a general framework to exhibit the relation of the asymptotic decay laws to certain dimensions of the orthogonality measure, that are defined via the divergence abscissas of suitable integrals. The unifying r?le of Mellin transform techniques in deriving classical and new results is underlined. Submitted: November 5, 2004. Accepted: January 6, 2006.     

A MIP approach for some practical packing problems: Balancing constraints and tetris-like items

This paper considers packing problems with balancing conditions and items consisting of clusters of parallelepipeds (mutually orthogonal, i.e. tetris-like items). This issue is quite frequent in space engineering and a real-world application deals with the Automated Transfer Vehicle project (funded by the European Space Agency), at present under development. A Mixed Integer Programming (MIP) approach is proposed. The three-dimensional single bin packing problem is considered. It consists of orthogonally placing, with possibility of rotation, the maximum number of parallelepipeds into a given parallelepiped. A MIP formulation of the problem is reported together with a MIP-based heuristic approach. Balancing conditions are furthermore examined, as well as the orthogonal placement (with rotation) of tetris-like items into a rectangular domain.Received: September 2003, Revised: February 2004, AMS classification: 90B99, 05B40, 90C90, 90C59Thanks are due to T. A. Ciriani for the important suggestions given for the whole paper and to S. Gliozzi (IBM, Business Consulting Services) for the significant support offered, in particular in discussing the topics presented in Sect. 2.1.     

The set union problem with dynamic weighted backtracking

We consider an extension of the set union problem, in which dynamic weighted backtracking over sequences of unions is permitted. We present a new data structure which can support each operation inO(logn) time in the worst case. We prove that this bound is tight for pointer based algorithms. Furthermore, we design a different data structure to achieve better amortized bounds. The space complexity of both our data structures isO(n). Motivations for studying this problem arise in logic programming memory management.Work partially supported by NSF Grant CCR-88-14977, by the ESPRIT II Basic Research Actions Program of the EC under contract No. 3075 (Project ALCOM), and by the Italian MURST Project Algoritmi e Strutture di Calcolo.Partially supported by an IBM Graduate Fellowship.     

On unitals in PG(2,q^2) stabilized by a homology group

The linear collineation group of a classical unital of $\mathrm{PG}(2,q^2)$ contains a group of homologies of order $q+1$ . In this paper we prove that if $\mathcal{U }$ is a unital of PG $(2,q^2)$ stabilized by a homology group of order $q+1$ and $q$ is a prime number, then $\mathcal{U }$ is classical.     

Extreme value theory for singular measures

In this paper, we perform an analytical and numerical study of the extreme values of specific observables of dynamical systems possessing an invariant singular measure. Such observables are expressed as functions of the distance of the orbit of initial conditions with respect to a given point of the attractor. Using the block maxima approach, we show that the extremes are distributed according to the generalised extreme value distribution, where the parameters can be written as functions of the information dimension of the attractor. The numerical analysis is performed on a few low dimensional maps. For the Cantor ternary set and the Sierpinskij triangle, which can be constructed as iterated function systems, the inferred parameters show a very good agreement with the theoretical values. For strange attractors like those corresponding to the Lozi and He?non maps, a slower convergence to the generalised extreme value distribution is observed. Nevertheless, the results are in good statistical agreement with the theoretical estimates. It is apparent that the analysis of extremes allows for capturing fundamental information of the geometrical structure of the attractor of the underlying dynamical system, the basic reason being that the chosen observables act as magnifying glass in the neighborhood of the point from which the distance is computed.     

Biologically Inspired C−H and C=C Oxidations with Hydrogen Peroxide Catalyzed by Iron Coordination Complexes

The development of catalysts for the selective oxidation of readily available hydrocarbons or organic precursors into oxygenated products is a long‐standing goal in organic synthesis. In the last decade, some iron coordination complexes have shown the potential to fit this role. These catalysts can mimic the O?O activation mode of far more sophisticated iron oxygenase enzymes, generating powerful yet selective oxidants. In this review, we report state‐of‐the‐art C?H and C=C oxidations catalyzed by non‐heme iron complexes and H₂O₂ as the oxidant. Finally, we briefly describe some novel oxidative reactivity and the perspectives of this chemistry.