Well‐Defined Silica‐Supported Mo–Alkylidene Catalyst Precursors Containing One OR Substituent: Methods of Preparation and Structure–Reactivity Relationship in Alkene Metathesis

Silica supports : Well‐defined silica‐supported Mo–alkylidene complexes containing one alkoxy/aryloxy substituent are selectively obtained by grafting onto silica either well‐defined molecular bis(alkoxy) or alkoxyamido complexes (see scheme). These silica‐supported complexes are highly efficient catalyst precursors for the metathesis of acyclic alkenes. However, they display poor performances in ring‐closing metathesis reactions, possibly due to the relatively large siloxy ligand (silica) inducing a greater rigidity.

     

Statistical optimization of the silylation reaction of a mercaptosilane with silanol groups on the surface of silica gel

Thiol-modified silica is often used as an intermediate product for further synthesis of modified stationary phases for chromatography or purification processes. Different conditions were used to synthesize such thiol-modified particles, but systematic optimizations remained scarce. In this study the reaction conditions for the synthesis of mercaptopropyl-modified silica were optimized. The general synthetic method consists in slurrying the silica gel in toluene before adding 3-mercaptopropyldimethoxymethylsilane together with a tertiary amine as catalyst (here dimethylaminopyridine). Reaction time and temperature were optimized using a full factorial design of experiment (DoE) from 3 to 25 h with temperature varying between 45 and 105 °C. The surface coverage of the silica with mercaptopropyl-groups was analyzed by two different ways (elemental analysis and chemical surface reaction with 2,2′-dipyridyl disulfide followed by HPLC-UV analysis of stoichiometrically liberated pyridyl-2-thione). We obtained a three-dimensional (3D) plot of the surface coverage as a function of reaction time and temperature. The arch-shaped hyperplane allowed us to determine an optimum with regard to time and temperature, which yields to the highest surface coverage possible. We also verified that the increase of the surface coverage does not lead to a decrease of the stability of the surface modification by subjecting the gels to treatment with high temperature and acidic conditions. The stability was monitored by different chromatographic methods. Moreover, ²⁹Si cross-polarization-magic angle spinning (CP-MAS) NMR spectra of materials prepared by different conditions allowed to confirm that the Si species on the surface were essentially the same, while there was only a minute difference in signal intensities for the individual Si species for materials obtained by distinct temperatures.     

VOPO4·H2O: a stacking faults structure studied by X-ray powder diffraction and DFT-D calculations

The dehydration process of VOPO(4)·2H(2)O occurs in two steps corresponding to successive elimination of the two crystallographically distinct water molecules. The intermediate phase VOPO(4)·H(2)O has been stabilized for X-ray powder diffraction studies. The resulting data suggest a tetragonal cell (a = 6.2203(2) ? and c = 6.18867(7) ?), but an important anisotropy in the line broadening points out the necessity of considering a not perfectly organized structure. Because of the layered structure of this compound, density functional theory calculations including dispersion corrections have been carried out to evaluate the possible presence of stacking faults. The results of these calculations give information about the nature of the translations and their probabilities using a Boltzmann distribution. DIFFaX+ simulations of the X-ray powder diffraction pattern have been carried out using the results of the theoretical calculations and confirm the presence and nature of stacking faults.     

Synthesis of Polycyclic Aromatic Hydrocarbon‐Based Nanovehicles Equipped with Triptycene Wheels

Two new nanovehicles that have extended aromatic platforms as the cargo zones have been obtained. Two strategies were considered for the formation of the perylene core from two naphthalene precursors. The first was based on a Scholl‐type reaction involving an oxidant, and the second used a brominated derivative to perform a homocoupling reaction. The first strategy failed under diverse coupling conditions in the presence of several strong oxidants. Nevertheless, the use of CoF₃ in trifluoroacetic acid triggered a dimerization reaction between two ester groups of one molecule and the naphthalene unit of another, thereby surprisingly yielding a ten‐membered carbon macrocycle. The second strategy encountered a lack of reactivity of the substrate under several homocoupling conditions. The dimerization was not easily performed but Ullmann‐type conditions ultimately gave the expected product. The low yield and low solubility of the product encouraged us to modify our initial design. The synthesis of a new chassis that incorporated additional tert‐butyl groups improved the solubility of the molecules and also prevented overcyclization of the aromatic platform by blocking these positions. Some p‐phenylene spacers were also intercalated between the iodine and perylene centers to increase the reactivity of the halide towards coupling reactions. Two new chassis were obtained by Scholl‐type oxidative coupling using FeCl₃ as the oxidant. The introduction of four triptycene wheels allowed the formation of the two corresponding nanovehicles.     

Thermo‐plasmonics: using metallic nanostructures as nano‐sources of heat

Recent years have seen a growing interest in using metal nanostructures to control temperature on the nanoscale. Under illumination at its plasmonic resonance, a metal nanoparticle features enhanced light absorption, turning it into an ideal nano‐source of heat, remotely controllable using light. Such a powerful and flexible photothermal scheme is the basis of thermo‐plasmonics. Here, the recent progress of this emerging and fast‐growing field is reviewed. First, the physics of heat generation in metal nanoparticles is described, under both continuous and pulsed illumination. The second part is dedicated to numerical and experimental methods that have been developed to further understand and engineer plasmonic‐assisted heating processes on the nanoscale. Finally, some of the most recent applications based on the heat generated by gold nanoparticles are surveyed, namely photothermal cancer therapy, nano‐surgery, drug delivery, photothermal imaging, protein tracking, photoacoustic imaging, nano‐chemistry and optofluidics.     

Phase transitions in 3,5-dichloropyridine

Abstract

Structural phase transitions in 3,5-dichloropyridine crystal have been studied by calorimetry (150–300 K), X-ray diffraction (300 K), ³⁵Cland ¹⁴N nuclear quadrupole resonance (75–300 K) and vibrational spectroscopy (20–300K). Three phases have been shown to exist: phase I, between 338 and 287.5 K, phase 11, between 287.5 and 167.5 K, and phase 111, below 167.5 K. Phase I is characterised by the space group P 2,/m and Z = 2 whereas phases I1 and 111 remain centrosymmetric but double the unit cell. All the phases are ordered and contain crystallo- graphically equivalent molecules. The I ? I1 transition is of first order and probably of the reconstructive type while the II ? III transition is believed to be displacive. Both transitions are monitored by predominantly R′_x and R′_z librational motions.     

The forest associated with the record process on a Lévy tree

We perform a pruning procedure on a Lévy tree and instead of throwing away the removed sub-tree, we regraft it on a given branch (not related to the Lévy tree). We prove that the tree constructed by regrafting is distributed as the original Lévy tree, generalizing a result of Addario-Berry, Broutin and Holmgren where only Aldous’s tree is considered. As a consequence, we obtain that the “average pruning time” of a leaf is distributed as the height of a leaf picked at random in the Lévy tree.     

Challenging 50 years of established views on Ugi reaction: a theoretical approach

The Ugi reaction is one of the most famous multicomponent couplings, and its efficiency is still explained by the original mechanism suggested by Ugi in the 60s. This article aims to present a thorough theoretical study of this reaction. It describes how the imine is activated and how the new stereogenic center is formed. Our calculations strongly suggest alternatives to some commonly accepted features, such as the reversibility of the intermediate steps, and temper the nature of the driving force of the reaction.     

Radical one-pot α,β-dual and β-mono-oxymethylation of alkylidenemalonate

Dimethylzinc-mediated radical conjugate addition reaction of dimethyl alkylidenemalonates with iodomethyl pivalate gave a high yield of the α,β-dual oxymethylation product in one pot under air and the β-pivaloyloxymethylation product under argon.     

A notion of geometric complexity and its application to topological rigidity

We introduce a geometric invariant, called finite decomposition complexity (FDC), to study topological rigidity of manifolds. We prove for instance that if the fundamental group of a compact aspherical manifold M has FDC, and if N is homotopy equivalent to M, then M×ℝ ⁿ is homeomorphic to N×ℝ ⁿ , for n large enough. This statement is known as the stable Borel conjecture. On the other hand, we show that the class of FDC groups includes all countable subgroups of GL(n,K), for any field K.