A precise jab to methane: The SO(2)(*+) radical cation (see figure) effectively activates CH(4) at room temperature through a [H(3)C(*)...HOSO(+)] methyl intermediate isolated in the gas phase by mass spectrometry. Methanol and ionized methyl hydrogen sulfoxylate, CH(3)OSOH(*+), are formed by selective, direct attack of the incipient methyl radical at the O atom of the intermediate. The reaction shows radical and charge effects in the activation of methane by metal-free radical cations.
The solubility parameter of a series of methyl esters of fatty acids, the components of biodiesel, was calculated using the group incremental method proposed by Van Krevelen. The solubility parameter of biodiesel was compared with that of a series of rubbers like EPDM, butyl rubber, polyisoprene, polybutadiene, SBR (with different content of styrene), and nitrile rubber (with different content of acrylonitrile) showing that biodiesel is an effective solvent of all the above mentioned rubbers with the exclusion of nitrile rubber. Indeed, it was experimentally verified that polyisoprene, polybutadiene and SBR are easily soluble in biodiesel while polystyrene gives a cloudy solution. Considerations on the solubility parameter of the biodiesel and of a series of rubbers have led to the conclusion that biodiesel behaves essentially as an internal lubricant in a diene rubber matrix, the same situation occurs with the common aromatic mineral oil plasticizer known as T-RAE. The experimental evaluation of biodiesel as plasticizer in an SBR-based rubber compound in comparison to an aromatic mineral oil have led to the primary conclusion that biodiesel is reactive with the sulphur curing agent subtracting sulphur to the crosslinking polymer chains and leading to a vulcanizatewith lower moduli, tensile and hardness and higher elongationsin comparison to a reference compound fully plasticized with an aromatic mineral oil. However, biodiesel seems a good low temperature plasticizer because the low elastic modulus observed is desired in a winter tire tread for a good grip on snow and ice. The present work is only an exploratory work, and the tire tread formulation with biodiesel was not optimized.
A series of α, ω-diphenylpolyynes were synthesized through the Cadiot Chodkiewicz reaction starting from Cu(I)-phenylacetylide and diiodoacetylene. The complete series of diphenylpolyynes Phi-(CC)n-Phi with n = 2,3,4 and 5 was obtained and analyzed by electronic absorption spectroscopy, liquid chromatography (HPLC-diode array) and FT-IR spectroscopy. The diphenylpolyynes when treated with nascent hydrogen produced by the action of HCl on Zn dust are changed into a mixture of diphenylpolyenes as shown by UV spectroscopy and HPLC
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