Glycosylation of Volatile Phenols in Grapes following Pre-Harvest (On-Vine) vs. Post-Harvest (Off-Vine) Exposure to Smoke

Taint in grapes and wine following vineyard exposure to bushfire smoke continues to challenge the financial viability of grape and wine producers worldwide. In response, researchers are studying the chemical, sensory and physiological consequences of grapevine smoke exposure. However, studies involving winemaking trials are often limited by the availability of suitable quantities of smoke-affected grapes, either from vineyards exposed to smoke or from field trials involving the application of smoke to grapevines. This study compared the accumulation of volatile phenol glycosides (as compositional markers of smoke taint) in Viognier and Cabernet Sauvignon grapes exposed to smoke pre- vs. post-harvest, and found post-harvest smoke exposure of fruit gave similar levels of volatile phenol glycosides to fruit exposed to smoke pre-harvest. Furthermore, wines made from smoke-affected fruit contained similar levels of smoke-derived volatile phenols and their glycosides, irrespective of whether smoke exposure occurred pre- vs. post-harvest. Post-harvest smoke exposure therefore provides a valid approach to generating smoke-affected grapes in the quantities needed for winemaking trials and/or trials that employ both chemical and sensory analysis of wine.     

Localized versus diffuse damage in amorphous materials

Based on a Griffith approach, we study the behavior of disordered media constituted at the microscale by distributions of elastic and breakable links with variable activation and fracture thresholds. Depending on the microscopic distribution properties, the material may be characterized by an unstable strain domain, which gives the possibilities of having homogeneous or localized damage. Our simple model delivers a theoretical scheme to describe main experimental effects observed at the microstructure and macroscopic scale in disordered materials undergoing damage and relates them to the inhomogeneity properties of the material.     

Electrochemical Organic Synthesis of Electron-Rich Biaryl Scaffolds: An Update

Biaryl scaffolds are widely spread in biologically important natural products, in numerous therapeutic agents, but they are also considered a privileged class of ligands and (organo)catalysts; therefore, the development of efficient alternative methodologies to prepare such compounds is always attracting much attention. The present review discusses the organic electrosynthesis of biaryls starting from phenols, anilines, naphthols, and naphthylamines. The most significant examples of the works reported in the last decade are presented and classified according to the single class of molecules: after the introduction, the first three sections relate to the reactions of phenols, naphthols, and anilines, respectively; the other two sections refer to cross-coupling and miscellaneous reactions.     

Chemical reactions occurring in the thermal treatment of PC/PMMA blends

The chemical reactions occurring in the thermal treatment of bisphenol-A polycarbonate (PC) and poly(methyl methacrylate) (PMMA) blends have been investigated by nuclear magnetic resonance (NMR), mass spectrometry (MS), size exclusion chromatography (SEC), and thermogravimetry (TG). Our results suggest that in the melt-mixing of PC/PMMA blends, at 230°C, no exchange reactions occur and that only the depolymerization reaction of PMMA has been observed. In the presence of an ester-exchange catalyst (SnOBu₂), an exchange reaction was found to occur at 230°C, but no trace of PC/PMMA graft copolymer has been observed. Instead, an exchange reaction between the monomer methyl methacrylate (MMA), generated in the unzipping of PMMA chains, and the carbonate groups of PC has been suggested. This is due to the diffusion of MMA at the interface or even into the PC domains, where it can react with PC producing low molar mass PC oligomers bearing methacrylate and methyl carbonate chain ends and leaving the undecomposed PMMA chains unaffected. The TG curves of PC/PMMA blends prepared by mechanical mixing and by casting from THF show two separated degradation steps corresponding to that of homopolymers. This behavior is different from that of a transparent film of PC/PMMA blend, obtained by solvent casting from DCB/CHCl₃, which shows a single degradation step indicating that the degradation rate of PC is increased by the presence of PMMA in the blend. The thermal degradation products obtained by DPMS of this blend consist of methyl methacrylate (MMA), cyclic carbonates arising from the degradation of PMMA and PC, respectively, and a series of open chain bisphenol-A carbonate oligomers with methacrylate and methyl carbonate terminal groups. The presence of the latter compounds suggests a thermally activated exchange reaction occurring above 300°C between MMA and PC. The presence of bisphenol-A carbonate oligomers bearing methyl ether end groups, generated by a thermally activated decarboxylation of the methyl carbonate end groups of PC, has also been observed among the pyrolysis products. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1873–1884, 1998     

Thermal decomposition processes in aromatic polythiocarbonates

The thermal degradation of some polythiocarbonates obtained from bisphenol A bischloroformate and dithiols have been investigated by thermogravimetry and by direct pyrolysis in the mass spectrometer operating both in electron and chemical ionization. Poly(bisphenol A-co-tri-methylenedithiocarbonate) decomposes by an intramolecular exchange process (back-biting) producing trimethylene-1,3-dithiocarbonate and bisphenol A polycarbonate. The latter undergoes further thermal degradation at higher temperature yielding cyclic oligomers. Polymers containing tetramethylene-1,4-dithiocarbonate and hexamethylene-1,6-dithiocarbonate units decompose by the same mechanism, but the elimination of the dithiocarbonate units is not as fast and selective as the previous case. Some bisphenol A units are eliminated in the first thermal degradation stage and a rearrangement reaction producing ether linkage also occurs. Poly(phenylene-1,3-dithiocarbonate) decomposes by CO and COS loss with formation of sulfide and disulfide bridges along the polymer chains, which undergo further thermal degradation by a back-biting process yielding a series of cyclic compounds. The thermal degradation of Poly(bisphenol A-co-phenylenedithiocarbonate) takes place through an interchange reaction producing phenylene-1,3-dithiocarbonate sequences which further decompose as the corresponding polymer. The remaining bisphenol A polycarbonate decomposes at higher temperature producing cyclic carbonates.     

Effect of ion energy on the implantation products of benzene

Solid benzene has been implanted with inert-gas ions with energies ranging from 16 to 100 keV. The small variation observed in the relative concentration of the products has been found to depend mainly on the fact that the relative weight of the nuclear and electronic stopping mechanisms is changing along the energy range explored.