Olefin metathesis: what have we learned about homogeneous and heterogeneous catalysts from surface organometallic chemistry?

Since its early days, olefin metathesis has been in the focus of scientific discussions and technology development. While heterogeneous olefin metathesis catalysts based on supported group 6 metal oxides have been used for decades in the petrochemical industry, detailed mechanistic studies and the development of molecular organometallic chemistry have led to the development of robust and widely used homogeneous catalysts based on well-defined alkylidenes that have found applications for the synthesis of fine and bulk chemicals and are also used in the polymer industry. The development of the chemistry of high-oxidation group 5–7 alkylidenes and the use of surface organometallic chemistry (SOMC) principles unlocked the preparation of so-called well-defined supported olefin metathesis catalysts. The high activity and stability (often superior to their molecular analogues) and molecular-level characterisation of these systems, that were first reported in 2001, opened the possibility for the first direct structure–activity relationships for supported metathesis catalysts. This review describes first the history of SOMC in the field of olefin metathesis, and then focuses on what has happened since 2007, the date of our last comprehensive reviews in this field.

Surface organometallic chemistry bridges the gap between homogeneous and heterogeneous olefin metathesis catalysts.     

Modeling sequence evolution with kernel methods

We model the evolution of biological and linguistic sequences by comparing their statistical properties. This comparison is performed by means of efficiently computable kernel functions, that take two sequences as an input and return a measure of statistical similarity between them. We show how the use of such kernels allows to reconstruct the phylogenetic trees of primates based on the mitochondrial DNA (mtDNA) of existing animals, and the phylogenetic tree of Indo-European and other languages based on sample documents from existing languages. Kernel methods provide a convenient framework for many pattern analysis tasks, and recent advances have been focused on efficient methods for sequence comparison and analysis. While a large toolbox of algorithms has been developed to analyze data by using kernels, in this paper we demonstrate their use in combination with standard phylogenetic reconstruction algorithms and visualization methods.     

All tilting modules are of finite type

We prove that any infinitely generated tilting module is of finite type, namely that its associated tilting class is the Ext-orthogonal of a set of modules possessing a projective resolution consisting of finitely generated projective modules.

     

Complete charge pooling is prevented in viologen-based dendrimers by self-protection

We have investigated the electrochemical behavior, and chemical and photosensitized reduction of two dendrimers based on a 1,3,5-trisubstituted benzenoid core, which contain 9 and 21 4,4'-bipyridinium (usually called viologen) units, respectively, in their branches and are terminated with tetraarylmethane groups. For comparison purposes, the behavior of reference compounds that contain a single viologen unit have also been investigated. We have found that only part of the viologen units can be reduced in the dendrimer species. For the larger dendrimer, the number of reducible viologens (out of the 21 present) is 14 in electrochemical experiments (in MeCN), 9 on reduction with bis(benzene)chromium (in MeCN), and 13 by photoinduced electron transfer with 9-methylanthracene as a photosensitizer and triethanolamine as a sacrificial reductant in CH2Cl2. The reduced viologen units undergo partial dimerization. The photochemical experiments have shown that only monomeric, one-electron-reduced viologen units are formed at the beginning of the irradiation, followed by dimer formation, until a photostationary state is reached that contains 40 % nonreduced, 33 % monomeric reduced, and 27 % reduced units associated in the dimeric form. The results suggest that, upon reduction of a fraction of the viologen units, the dendrimer structure shrinks, with the result that the bulky terminal groups protect other viologen units from being reduced.     

Stability of a NDIR analyser for CO2 at atmospheric concentration

Carbon dioxide monitoring is significant in the environmental field since this gas plays an important role in the greenhouse effect. In order to determine CO2 concentration and to develop simulation models, it is necessary to carry out measurements which are accurate and comparable in time and space, i.e. SI-traceable. Non-dispersive infrared (NDIR) analysers are employed for CO2 measurements, as they are precise and stable. In order to achieve traceability, such instruments have to be characterized and calibrated. At the Istituto di Metrologia "G. Colonnetti"--CNR, a procedure for calibrating NDIR analysers for CO2 at atmospheric level was developed, which enables to calculate a correction for the analyser output. In addition, a complete uncertainty analysis was carried out and a correct traceability chain was established. The goal of the present work is the study of the stability of a NDIR analyser by repeating calibrations during three years and comparing the correction curves obtained to identify a proper re-calibration interval for such analysers. The investigated instrument has good repeatability and reproducibility, hence satisfactory stability during time, as shown by the short-term and long-term compatibility of calibration curves.