170,078 research outputs found

    SINGLET OXYGEN IN THE PHOTODEGRADATION OF LIGNIN MODELS

    No full text
    The photochemical oxidation of lignin models in the presence of singlet oxygen nas studied. The treatment of the non-phenolic beta-O-4 aryl ether derivatives 6, 7, and 8 in the presence of both oxygen and Rose Bengal gave products deming from a formal beta-C-O cleavage formation. By this way the derivatives 12. 13, and 15 were obtained, The photochemical oxidation of the phenolic beta-O-4 aryl ehter 9 gave the same type of product confirming that, in this case, the presence of the carbonyl group is not indispensable to have the cleavage reaction. The use of the model compound 10 showed that. When the phenoxy part of the molecule shows a lower reactivity towards singlet oxygen, the oxidation of the phenol moiety to hydroquinone call occur. The photochemical behaviour of these model compounds can be rationalised from a reaction of singlet oxygen with the phenoxy part of the molecule. (C) 1997 Published by Elsevier Science Ltd

    Photodegradation of lignin: The role of singlet oxygen

    No full text
    The photochemical irradiation of some phenoxyacetophenone derivatives in the presence of oxygen by using visible light did not produce any decomposition product. In the presence of singlet oxygen, sensitized by using Bengal Rose, decomposition products were obtained. The products obtained were similar to those obtained by direct beta-C-O cleavage on the substrate. In this case, the observed behavior can be explained assuming an attack of singlet oxygen on a phenoxy part of the molecule

    Chemistry and materials. Italic 4. Wood, 100 years of structural studies

    No full text
    Nonostante la prima caratterizzazione strutturale della lignina risalga al 1908 molto è ancora ignoto circa la struttura dei materiali lignocellulosici. Italic 4 ha dedicato una sessione agli avanzamenti nel settore, focalizzata principalmente sull’identificazione e caratterizzazione di interazioni supramolecolari in biopolimeri vegetali

    A novel and efficient catalytic epoxidation of monoterpenes by homogeneous and heterogeneous methyltrioxorhenium in ionic liquids

    No full text
    A convenient and efficient synthesis of monoterpene epoxides by application of methyltrioxorhenium and heterogeneous poly(4-vinylpyridine)/methyltrioxorhenium and microencapsulated polystyrene/methyltrioxorhenium catalytic systems in ionic liquids is described here. It was found that even highly sensitive terpenic epoxides were obtained in excellent yields. Environmentally friendly, easily available and low cost (UHP) urea hydrogen peroxide adduct was used as the primary oxidant. Catalysts were stable systems for at least four recycling oxidations. Experimental results showed that the reactions performed in ionic liquids were more selective and efficient than the ones performed in molecular solvents. (c) 2009 Elsevier B.V. All rights reserved

    Catalytic MTO-based C-H insertion reactions of hydrogen peroxide: An investigation on the polymeric support role in heterogeneous conditions

    No full text
    Polymer-supported methyltrioxorhenium (MTO) compounds are shown to act as efficient and selective catalysts for the oxy-functionalization of C-H bonds in representative hydrocarbon derivatives (leading to the corresponding alcohols or ketones), using H2O2 as oxidant. The different supports used for the heterogenation of MTO, such as poly(4-vinylpyridine), poly(4-vinylpyridine)-N-oxide and polystyrene resins, all showed different catalytic behaviour in terms of substrate conversion and product yield, depending on the experimental conditions used. It is noteworthy that the novel heterogeneous catalysts were found to be stable, it being possible to effect their recover and recycle at least five times without appreciable loss of activity
    corecore