Small-angle X-ray scattering from styrene-butadiene-styrene block copolymers

Abstract

A new type of time-dependent and strain-history-dependent viscoelasticity was discovered in semidilute polymer solutions. Dynamic moduli G′ and G″ of 20% and 10% nitrile butadiene rubber (NBR) solutions were recorded as a function of time while oscillatory shear deformations were maintained. The moduli decrease with time was observed only at lower frequencies. The time dependence of G′ was more pronounced than that of G″. At a higher temperature, the time dependence was extended toward higher frequencies also, and the time dependence became stronger. Lowering the concentration of solution gave a similar effect as increasing temperature. After the cessation of oscillations, a slow recovery was observed. The recovery was somewhat faster at the higher temperature. The time-dependent moduli and their recovery were explained by the change and recovery of structures associated with long branches and gels in the NBR. The structure change occurred at higher frequencies also, but it was not observed during the application of oscillation. Only in subsequent measurements at lower frequencies could the structure change be detected. Thus, the change may be regarded as strain history dependent. The mechanism of the structural change was explained with either the entanglement or osmotic pressure models, depending on concentration.     

Efficient and low-noise single-photon detection in 1550 nm communication band by frequency upconversion in periodically poled LiNbO3 waveguides

We demonstrate 1500 nm band single-photon detection with low dark-count noise and a potentially high efficiency, which may allow long distance and high-bit-rate quantum key distribution. By developing frequency upconversion devices based on periodically poled lithium niobate waveguides, which are specifically designed to use a pump wavelength longer than that of communication-band photons, we completely eliminate the dark-count noise caused by parasitic nonlinear processes in the waveguide. We observed an internal conversion efficiency as high as 40% and demonstrated scaling down to the single photon level while maintaining a background dark-count rate of 10(2)s(-1).     

Synthesis of (+)-altholactone, (+)-7-epi-altholactone, (−)-etharvensin,and (+)-alumheptolide-A using Pd-catalyzed carbonylation

Syntheses of (+)-altholactone isolated from Goniothalamus giganteus and its C-7 epimer (+)-7-epi-altholactone, (?)-etharvensin and (+)-alumheptolide-A were achieved. The lactone ring of these compounds was constructed using Pd-catalyzed carbonylation.     

Kinetic resolution of sterically hindered secondary alcohols catalyzed by aminophosphinite organocatalyst

Kinetic resolution of secondary alcohols by benzoylation using a phosphinite derivative of (1S,2R)-1-amino-2-indanol as the catalyst was investigated. The aminophosphinite catalyst is effective for the kinetic resolution of aryl cycloalkyl carbinols with a small number of examples for organocatalytic kinetic resolution to achieve resolution with s = up to 44. Although the benzoylation of phenylalkanols proceeded with a low selectivity, 1-arylalkanols bearing at least one substituent at the ortho position on the benzene ring or a branched alkyl group on the carbinol carbon were resolved with acceptable selectivity.     

pH-Dependent catalytic activity and chemoselectivity in transfer hydrogenation catalyzed by iridium complex with 4,4'-dihydroxy-2,2'-bipyridine

Transfer hydrogenation catalyzed by an iridium catalyst with 4,4'-dihydroxy-2,2'-bipyridine (DHBP) in an aqueous formate solution exhibits highly pH-dependent catalytic activity and chemoselectivity. The substantial change in the activity is due to the electronic effect based on the acid-base equilibrium of the phenolic hydroxyl group of DHBP. Under basic conditions, high turnover frequency values of the DHBP complex, which can be more than 1000 times the value of the unsubstituted analogue, are obtained (up to 81 000 h(-1) at 80 degrees C). In addition, the DHBP catalyst exhibits pH-dependent chemoselectivity for alpha,beta-unsaturated carbonyl compounds. Selective reduction of the C=C bond of enone with high activity are observed under basic conditions. The ketone moieties can be reduced with satisfactory activity under acidic conditions. In particular, pH-selective chemoselectivity of the C=O versus C=C bond reduction was observed in the transfer hydrogenation of cinnamaldehyde.     

Synthesis of Optically Active Polystyrene Catalyzed by Monophosphine Pd Complexes

Cationic Pd^II monophosphine complexes derived from α‐ and β‐cyclodextrins (CDs) promote the homopolymerization of styrene under carbon monoxide pressure. Although reversible CO coordination takes place under catalytic conditions according to ¹³C NMR studies with ¹³C‐enriched CO, both complexes catalyze the formation of CO‐free styrene polymers. These macromolecules display optical activity as a result of the presence of stereoregular sequences within the overall atactic polymer.     

The structures of three new shishididemniols from a tunicate of the family Didemnidae

Three new serinolipid derivatives, shishididemniols C (1), D (2), and E (3), were isolated as antibacterial constituents of a tunicate of the family Didemnidae. Their planar structures were elucidated by interpretation of NMR and MS data, whereas the absolute stereochemistry was determined by chemical conversions. Shishididemniols C (3), D (4), and E (5) exhibited antibacterial activity against the fish pathogenic bacterium Vibrio anguillarum.