Thermostable Trioxane-Dioxolane Copolymers Obtained with Boron Trifluoride: Acrylonitrile Complex as Initiator

Trioxane was copolymerized with small amounts of dioxolane in benzene in the presence of a boron trifluoride:a crylonitrile complex as initiator. The kinetics of reactions was expressed in terms of topoenergetic principles. The copolymerizations had no induction periods and the maximum reaction rate was found proportional to the square of both the initiator and monomers concentrations. A zwitterionic mechanism is suggested for initiation. The activation energy for the system with 5% dioxolane was determined as 18.3 kcal/mol. The melting behavior of the copolymers is briefly discussed as a function of the dioxolane initial content, and is indicative of the amorphous-crystalline coupling phenomenon. The copolymers with ～ 5% dioxolane are thermostable in air up to 250%deg; and are recommended for practical purposes.     

Reentrant phenomenon in cyanoaryl alkylthioxybenzoates and cyanobenzoyloxyphenyl alkylthiobenzoates

Abstract

Three new series of cyanoaryl 4-alkylthioxybenzoates have been synthesized and characterized. The 4-cyanophenyl series displays only transient mesomorphic properties while the 6-cyano-2-naphthyl and 4-cyanobiphenyl series exhibit the classical nematic and smectic A phases; a reentrant nematic phase is also found in the latter. Two other new series in which the position of the sulphur atom in the central rigid core has been varied were also prepared: the 4–[4′-cyanobenzoyloxy]-phenyl 4-alkylthiobenzoates and 4–[4′-alkylbenzoyloxy]phenyl 4-cyanothiobenzoates. As in the analogous benzoate series, the reentrant phenomenon with the sequence C, S_Are, N_re, S_A, N, I is observed with the nonyl derivatives. Comparisons between the alkoxybenzoates and the alkylthioxybenzoates are given.     

Novel C1-symmetric dibenzophosphole ligands: application in hydroformylation reactions

A new family of non-symmetrical disubstituted dibenzophospholes possessing different steric and electronic effects have been synthesized and characterized. Their preliminary evaluation in rhodium-catalyzed hydroformylation reactions is presented.     

Effects of hydrophobic polyhedral oligomeric silsesquioxane coating on water vapour barrier and water resistance properties of paperboard

The substitution of fossil based packaging materials with materials from renewable sources is a topic of current interest. Polyhedral oligomeric silsesquioxanes with fatty acid moieties can have a renewable content of more than 90 % and are therefore called bio-POSS. In this study the bio-POSS octa-(ethyl erucamide) silsesquioxane was coated on a paperboard substrate as a liquid coating. The water resistance and the water vapour barrier properties of the paperboard were improved. Samples on which the bio-POSS coating layer was dried at 80 °C had a slightly higher water resistance and water vapour barrier than samples dried at room temperature. UV treatment of the coating layer had little effect. Solid state ¹H-NMR of UV treated coatings showed no reaction of double bonds of bio-POSS in the coating layer. Multiple coating considerably enhanced the water resistance and water vapour barrier properties of the paperboard, due to an increase in the coating thickness and a reduction in number of pores on top coated surfaces.     

Photoinitiated cationic polymerisation of multifunctional systems

Different types of tridimensional polymer networks have been synthetised by photoinitiated cationic polymerisation of vinyl ether and epoxy-functionalised oligomers and polymers. The polymerisation kinetics was followed by real-time infrared (RTIR) spectroscopy, a technique that records directly conversion versus time profiles in a timescale as short as 1 s. The addition of a diacrylate monomer was shown to accelerate the ring-opening polymerisation of epoxidized polyisoprene, with formation of interpenetrating polymer networks having well contrasted properties. A dual polymer network has been generated by photocrosslinking of a polyisoprene functionalised with both epoxy and acrylate groups.     

Differential effects of various trivalent and pentavalent organic and inorganic arsenic species on glucose metabolism in isolated kidney cells

We have compared the acute toxicities of the trivalent arsenic species arsenite, oxophenylarsine (PhAsO), 2-chlorovinyloxoarsine (ClvinAsO), methyloxoarsine (MeAsO), and of the pentavalent arsenic species arsenate, methyl- and phenyl-arsonic acid in rat kidney tubules (RKT) and Madin-Darby canine kidney (MDCK) cells. In RKT, PhAsO (1 μmol I⁻¹, 60 min) almost completely (>90%) blocked gluconeogenesis without affecting cell viability as assessed by dye exclusion. In MDCK cells, PhAsO (2 μmol I⁻¹) markedly inhibited glucose uptake (60% of controls) within 30 min, while cell viability, as assessed by formazan formation, was not affected within 180 min. MeAsO and CIvinAsO were similarly effective to PhAsO in both RKT and MDCK cells. Estimated IC₅₀ values for the inhibition of gluconeogenesis were 0.55 (PhAsO), 0.69 (CIvinAsO) and 0.99 μmol I⁻¹ (MeAsO) and for the inhibition of glucose uptake 1.23 (PhAsO). 2.62 (CIvinAsO) and 6.99 μmol I⁻¹ (MeAsO). At longer storage times, aqueous solutions of MeAsO and of CIvinAsO, but not of PhAsO, gradually lost toxic activity in RKT and MDCK cells, especially at alkaline pH. Concomitantly, a gradual decrease in content as assessed by HPLC was detected. Roughly 10-fold higher concentrations of arsenite than of PhAsO were required for comparable effects on gluconeogenesis in RKT, whereas in MDCK cells about 100-fold higher concentrations were needed for similar inhibition of glucose uptake. Pentavalent arsenate and phenylarsonate were two orders of magnitude less effective than PhAsO in RKT, while methylarsonate had virtually no influence on gluconeogenic activity. In MDCK cells the pentavalent arsenic species showed effects only in the millimolar range. It is concluded (1) that different mechanisms are involved in the acute toxicity of oxoarsines and inorganic arsenic and (2) that PhAsO offers advantages as a model substance for mono-substituted trivalent arsenicals, because it is more stable and more readily detectable.     

Ring-opening metathesis copolymerization employing ruthenium-based metathesis catalysts

The copolymerization of both high- and low-strain cyclic olefins employing three ruthenium-based metathesis catalysts is desribed. The effect of the ligand environment as well as the nature of the carbene on the copolymerizations is discussed.