Towards controlled cationic polymer growth from inorganic oxide defects: Directing the mechanism of polystyrene grafting from γ-irradiated silica

Most studies on surface-initiated controlled polymerizations for the synthesis of polymeric covalent organic-inorganic hybrid materials focus on chemical methods requiring specific modifications of the inorganic substrate. Few mechanistically-aware approaches have been undertaken towards exploiting the reactivity of defects induced by physical techniques such as ionizing radiations or UV–Vis light. Within this framework, we take grafted polymerization of styrene from γ-irradiated silica as a mechanistic testing ground where para- and diamagnetic silica defects are present, and polymerization proceeds through both radical and cationic mechanisms, resulting in a bimodal molecular weight distribution. We show that these mechanistic intricacies can be sorted out by resorting to the chemical arsenal developed in the last decades for controlled polymerizations. Specifically, we obtained a silica-polystyrene grafted material by cationic grafting from at 30 °C, a unimodal molecular weight distribution, and a relatively high molecular weight (Mn = 7.4 kDa) with a PDI of 1.68.     

Camptothecin‐7‐yl‐methanthiole: Semisynthesis and Biological Evaluation

The introduction of a methylenthiol group at position 7 of camptothecin was carried out in four steps. This preparation also yielded the corresponding disulfide, which behaves as a prodrug due to its reactivity with glutathione. Assessment of their antiproliferative activities, investigations of their mechanism of action, and molecular modeling analysis indicated that the 7‐modified camptothecin derivatives described herein maintain the biological activity and drug–target interactions of the parent compound.     

Microsomal lipid peroxidation: Effect of vitamin E and its functional interaction with phospholipid hydroperoxide glutathione peroxidase

The role of vitamin E in the protection against iron dependent lipid peroxidation was studied in rat liver microsomes and Triton-dispersed microsomal lipid micelles. In these systems, an antioxidant effect of vitamin E at a physiological ratio to phospholipids could be observed only in the presence of phospholipid hydroperoxide glutathione peroxidase (PHGPX) and glutathione. The rationale of this cooperation is discussed on the basis of the hydroperoxyl radical scavenging capacity of vitamin E and the reduction of membrane hydroperoxides by PHGPX. The scavenging of lipid hydroperoxyl radicals by vitamin E, although inhibiting propagation of the peroxidative chain, produces lipid hydroperoxides from which ferrous iron generates alkoxyl radicals that react with vitamin E almost as fast as with fatty acids. Therefore, only if membrane hydroperoxides are continuously reduced by this specific peroxidase does the scavenging of hydroperoxyl radicals by vitamin E lead to an effective inhibition of lipid peroxidation.     

Ozonolysis of α-PINENE, β-PINENE,d- and l-Turpentine Oil Studied by Chirooptical Methods; Some Implications on the Atmospheric Chemistry of Biogenic Volatile Organic Compounds

The main constituents of biogenic volatile organic compounds (BVOC) released in the atmosphere from vegetation are terpenes. The most common terpenes are α-pinene and β-pinene. These molecules react with ozone, forming oxidized derivatives which have low vapor pressure and which nucleate into secondary organic aerosol (SOA). Such aerosol-forming reactions have been simulated in the gas phase on laboratory scale with the visualization of the formation of SOA. Electronic absorption spectroscopy shows that the UV peak of pinenes at 205 nm is shifted to 225 nm during and after ozonolysis and is accompanied by a series of spectral features in the near infrared region (between 850 nm and 1100 nm). Optical rotatory dispersion (ORD) spectra were recorded on pure β(+)pinene and β(?)pinene. After ozonolysis β-pinene enantiomers are converted into nopinone enantiomers. The ORD spectra of both (?)nopinone and (+)nopinone respectively were recorded. The former showed a peak at 453 nm, an inflection point at 430 nm and a trough at 405 nm. The ORD spectrum of (?)-nopinone appears completely symmetrical to that of (+)nopinone. Thus, ORD spectroscopy can distinguish between BVOC and oxidized BVOC quite easily at least in the case of β-pinene. The ORD spectra of α-pinene enantiomers are different from those of β-pinene enantiomers and although the ORD spectra of ozonized α-pinene are not easily distinguishable from those of the primary compounds, they are completely different from those of ozonized β-pinene enantiomers. A reasonable natural model of BVOC is offered by l- and d-turpentine oil whose composition reflects that of the BVOC from conifer forests. The ORD spectra of ozonized l- and d-turpentine has permitted to distinguish between the levorotatory and dextrorotatory oxidation products and showing the ketone peak at about 367–380 nm, thus permitting in a real model to distinguish between primary BVOC (turpentine) and oxidized BVOC (or SOA) corresponding to ozonized turpentine. It has been proposed that ORD spectra in the gas phase could be used to detect chiral BVOC and oxidized chiral BVOC.     

Polarized Backward Raman Amplification in Randomly Birefringent Fibers

In this paper, a model describing the vector interaction of an intense backward-propagating Raman pump and a weak forward-propagating Stokes signal in randomly birefringent fibers is proposed. The model accounts for the losses, the Raman interaction, and the linear and nonlinear birefringence. Realistic characteristics of the backward-propagation-birefringence vector have been originally accounted for. Numerical solutions show that polarized-backward-Raman amplifiers can have gain fluctuations larger than previously reported because of linear- and nonlinear-birefringence effects. Moreover, the gain mean depends on the signal and pump state of polarization imposed at the amplifier input or output. Simple formulas are derived for predicting the gain mean when nonlinear effects can be neglected     

Nanoscale characterization of the biomechanical hardening of bovine zona pellucida

The zona pellucida (ZP) is an extracellular membrane surrounding mammalian oocytes. The so-called zona hardening plays a key role in fertilization process, as it blocks polyspermy, which may also be caused by an increase in the mechanical stiffness of the ZP membrane. However, structural reorganization mechanisms leading to ZP''s biomechanical hardening are not fully understood yet. Furthermore, a correct estimate of the elastic properties of the ZP is still lacking. Therefore, the aim of the present study was to investigate the biomechanical behaviour of ZP membranes extracted from mature and fertilized bovine oocytes to better understand the mechanisms involved in the structural reorganization of the ZP that may lead to the biomechanical hardening of the ZP. For that purpose, a hybrid procedure is developed by combining atomic force microscopy nanoindentation measurements, nonlinear finite element analysis and nonlinear optimization. The proposed approach allows us to determine the biomechanical properties of the ZP more realistically than the classical analysis based on Hertz''s contact theory, as it accounts for the nonlinearity of finite indentation process, hyperelastic behaviour and material heterogeneity. Experimental results show the presence of significant biomechanical hardening induced by the fertilization process. By comparing various hyperelastic constitutive models, it is found that the Arruda–Boyce eight-chain model best describes the biomechanical response of the ZP. Fertilization leads to an increase in the degree of heterogeneity of membrane elastic properties. The Young modulus changes sharply within a superficial layer whose thickness is related to the characteristic distance between cross-links in the ZP filamentous network. These findings support the hypothesis that biomechanical hardening of bovine ZP is caused by an increase in the number of inter-filaments cross-links whose density should be higher in the ZP inner side.     

Sheathed cold-formed steel housing: A seismic design procedure

Nowadays, different research teams are engaged on experimental and theoretical studies having as main aim the evaluation of seismic performance of sheathed cold-formed steel frame structures. Although a relatively large number of experimental and theoretical studies are available, the development of useful tools for the seismic design should be improved. As an attempt to overcome this lack, this paper aims to present a structural design procedure that allows, through the definition of three design nomographs, the screw spacing and all the shear walls components to be obtained on the basis of linear dynamic or nonlinear static seismic analysis. In addition, a procedure for the prediction of the whole pushover response curve of sheathed cold-formed steel shear walls, which can be advantageously used for developing the design nomographs, is presented.     

Radiation-Induced Synthesis of Fullerene-Silica Hybrid Nanomaterials

C₆₀ fullerene has been radiation grafted on bare and functionalized silica surface with mercaptopropyl moieties in toluene solution. The resulting fullerene-silica hybrid nanomaterials have been characterized by FT-IR and solid state ¹³C CP-MAS NMR spectroscopy and compared to the radiolysis products of C₆₀ in toluene. It has been found that fullerene is grafted on silica surface but, because the radiation grafting has been conducted in toluene, fullerene results arylated from radicals derived from toluene radiolysis. The fullerene-silica hybrid nanomaterials cannot be extracted by warm decalin, demonstrating that the fullerene cage is chemically bonded on the silica surface. The thermal behavior of fullerene-silica hybrid nanomaterials has been studied by thermogravimetric analysis (TGA) and differential thermal analysis (DTA) in air flow.