Kinetics of the gas-phase reactions of the OH radical with (C2H5)3PO and (CH3O)2P(S)Cl at 296 ± 2 K

The kinetics of the gas-phase reactions of the OH radical with (C₂H₅O)₃PO and (CH₃O)₂P(S)Cl and of the reactions of NO₃ radicals and O₃ with (CH₃O)₂P(S)Cl have been studied at room temperature. Using a relative rate technique, the rate constants determined for the reactions of the OH radical with (C₂H₅O)₃PO and (CH₃O)₂P(S)Cl at 296 ± 2 K and 740 torr total pressure of air were (5.53 ± 0.35) × 10^?11 and (5.96 ± 0.38) × 10^?11 cm³ molecule^?1 s^?1, respectively. Upper limits to the rate constants for the NO₃ radical and O₃ reactions with (CH₃O)₂P(S)Cl of <3 × 10^?14 cm³ molecule^?1 s^?1 and <2 × 10^?19 cm³ molecule^?1 s^?1, respectively, were obtained. These data are compared and discussed with previous literature data for organophosphorus compounds.     

Formation of ring-retaining products from the OH radical-initiated reactions of benzene and toluene

The aromatic ring-retaining products formed from the gas–phase reactions of the OH radical with benzene and toluene, in the presence of NO_x, have been identified and their formation yields determined. These products, and their formation yields, are as follows: from benzene – phenol, 0.236 ± 0.044; nitrobenzene, {(0.0336 ± 0.0078) + (3.07 ± 0.92) × 10^?16[NO₂]}; from toluene – benzaldehyde, 0.0645 ± 0.0080; benzyl nitrate, 0.0084 ± 0.0017; o?cresol, 0.204 ± 0.027; m? + p?cresol, 0.048 ± 0.009; m-nitrotoluene, {(0.0135 ± 0.0029) + (1.90 ± 0.25) × 10^?16[NO₂]}, where the NO₂ concentration is in molecule cm^?3 units. The formation yields of o- and p-nitrotoluene from toluene were ca. 0.07 and 0.35 that of m-nitrotoluene, respectively. The observations that the nitro-aromatic yields do not extrapolate to zero as the NO₂ concentration approaches zero are not consistent with current chemical mechanisms for these OH radical-initiated reactions, and suggest that under the experimental conditions employed in this study the hydroxycyclohexadienyl radicals formed from OH radical addition to the aromatic ring react with NO₂ rather than with O₂. However, these data concerning the nitroaromatic yields are consistent with our previous conclusions that many of the nitrated polycyclic aromatic hydrocarbons present in ambient air are formed, at least in part, in the atmosphere from OH radical reactions.     

Quasitriangular Hopf algebras whose group-like elements form an abelian group

In this paper we prove some properties of the set of group-like elements of , , for a pointed minimal quasitriangular Hopf algebra over a field of characteristic 0, and for a pointed quasitriangular Hopf algebra which is indecomposable as a coalgebra. We first show that over a field of characteristic 0, for any pointed minimal quasitriangular Hopf algebra , is abelian. We show further that if is a quasitriangular Hopf algebra which is indecomposable as a coalgebra, then is contained in , the minimal quasitriangular Hopf algebra contained in . As a result, one gets that over a field of characteristic 0, a pointed indecomposable quasitriangular Hopf algebra has a finite abelian group of group-like elements.

     

The effect of thiolation on the mechanical and protein adsorption properties of polyurethanes

Segmented polyurethanes are important polymers for a number of industrial and technological applications. The purpose of this work was to synthesize polybutadiene-based polyurethanes and subsequently graft carboxylate and sulfonate side chains via thiol-ene reaction. Spectroscopic investigations showed that grafting yielded good conversion for the vinyl unsaturation of the polybutadiene soft segment. DSC and tensile testing revealed that grafted polyurethanes had a better segmental compatibility and superior mechanical properties than the control polyurethane without grafting. The carboxylic side chains of the soft segment were responsible for the observed improved mechanical properties. Initial protein adsorption tests on these polymers were found to be higher than the control surface. The polyurethanes of the current study could be used for biomedical applications where protein attachment to the surface is needed for specific cell adhesion and tissue repair.     

Gas-Phase Silicon Alkoxide Reactivity vs. Na-Alginate Droplets for Conjugation of Alginate and Sol-Gel Technologies

Solutions with Na-alginate concentrations ranging from 0.5 to 2.5% w/v are processed to prepare Ca-alginate beads using a nozzle ejector under constant He-flow. Beads were spherical in shape and their size distributions were determined; in all samples the average diameter fell in the 120–140 μm interval. Volumetric yields were found to be linearly dependent of the original Na-alginate load whereas the bead diameters were almost constant, according to a constant hindrance of Ca-alginate macromolecular units in the final Ca-alginate gel. The rheology of Na-alginate solutions was studied, with determination of intrinsic viscosity; experimental evidence of microsphere formation, even at the lowest Na-alginate concentrations, indicated that ejection processing changes the rheological parameters controlling bead formation in ordinary dropping processing. Gaseous silicon alkoxides – Si(OEt)₄ and MeSi(OEt)₃ – carried by a He flow were deposited on Na-alginate droplets during ejection. The process was studied by continuous mass spectrometry analysis before and after Na-alginate ejection during the 5-min treatment; in all cases results indicated a deposition yield of 58%. Traces of alcohol in the mass spectrometry analysis of the out-flow gas excluded instantaneous formation of sol-gel silica on the Na-alginate droplets during their residence in the gas phase. For various Na-alginate concentrations, ethanol released by silica gel formation is constant as well as the amount of deposited SiO₂; a siliceous layer ranging from 0.08 to 0.17 μm thick on the surface of the Ca-alginate beads was calculated.     

Functionality and stability of heparin immobilized onto poly(dimethylsiloxane)

Poly(dimethylsiloxane) (PDMS) has become an attractive material when working in the field of microfluidics, mainly because of the rapid prototyping process it involves. The increased surface volume ratio in microchannels makes the interaction between sample and material surface highly important, evident when handling complex biological samples such as plasma or blood. This study demonstrates a new grade of non-covalent heparin surface that adds efficient anticoagulant property to the PDMS material. The surface modification is a simple and fast one-step process performed at neutral pH, optimal when working with closed microsystems. The heparin formed a uniform and functional coating on hydrophobic PDMS with comparatively high level of antithrombin-binding capacity. In addition, long-term studies revealed that the immobilized heparin was more or less stable in the microchannels over a time of three weeks. Recalcified plasma in contact with native PDMS showed complete coagulation after 1h, while no fibrin formation was detected in plasma incubated on heparin-coated PDMS within the same time. In conclusion, we see the heparin coating developed and evaluated in this study as a tool that greatly facilitates the use of PDMS in microfluidics dealing with plasma or blood samples.     

The stokes-kirchhoff relation in chemically reacting fluids

A generalized Kirchhoff-Stokes equation for the sound attenuation coefficient is derived from irreversible thermodynamics. The discrepancy between the experimental value of the absorption coefficient and the value calculated from the generalized equation is analyzed. In particular, the so-called effective bulk viscosity and the transport coefficient which links a chemical reaction to the viscous processes are emphasized. An experimental example illustrating the general situation is also given.     

Asymmetric synthesis of the stereoisomers of 2-amino-5-carboxymethyl-cyclopentane-1-carboxylate

The stereoisomers of 2-amino-5-carboxymethyl-cyclopentane-1-carboxylate may be prepared stereoselectively from diester derivatives of (E,E)-octa-2,6-diendioc acid, with the key step utilising the conjugate addition of homochiral lithium N-benzyl-N- alpha-methylbenzylamide. The trans-C(1)-C(2)-stereoisomers are readily prepared via a diastereoselective tandem conjugate addition cyclisation protocol with lithium (R)-N-benzyl-N- alpha-methylbenzylamide, with subsequent hydrogenolysis and ester hydrolysis giving the (1R,2R,5R)- and (1R,2R,5S)- beta-amino diacids in good yields. The preparation of the cis-C(1)-C(2)-stereoisomers utilises a protocol involving N-oxidation and Cope elimination of the major diastereoisomeric product arising from conjugate addition and cyclisation, giving homochiral (R)-5-carboxymethyl-cyclopentene-1-carboxylate. Conjugate addition of either lithium (R)- or (S)-N-benzyl-N- alpha-methylbenzylamide to (R)-5-carboxymethyl-cyclopentene-1-carboxylate, and diastereoselective protonation with 2,6-di-tert-butyl phenol gives, after hydrogenolysis and ester hydrolysis, the (1S,2R,5R)- and (1R,2S,5R)- beta-amino diacids in good yield. The use of (S)-N-benzyl-N- alpha-methylbenzylamide in the initial conjugate addition and cyclisation reaction, and subsequent repetition of the elimination and conjugate addition strategy allows stereoselective access to all stereoisomers of 2-amino-5-carboxymethyl-cyclopentane-1-carboxylate.     

Efficient microwave combinatorial parallel and nonparallel synthesis of N-alkylated glycine methyl esters as peptide building blocks

An easy and convenient microwave-assisted synthesis of N-alkylated glycine methyl esters is described. Parallel and nonparallel combinatorial methods are described and compared. The described reactions are reductive alkylations of several aldehydes and glycine methyl ester in the presence of NaBH3CN. Good yields and short reaction times are the main aspects of these procedures.     

Microwave-assisted synthesis of 1,3-dihydro-[1,2,5]thiadiazolo[3,4-b]pyrazine-2,2-dioxides

1,3-Dihydro[1,2,5]thiadiazolo[3,4-b]pyrazine-2,2-dioxides are obtained in a good yield from the reaction of 2,3-diamino pyrazines with sulfamide under microwave conditions.