Far-red triplet sensitized Z-to-E photoswitching of azobenzene in bioplastics

We report the first example of direct far-red triplet sensitized molecular photoswitching in a condensed phase wherein a liquid azobenzene derivative (Azo1) co-assembled within a liquid surfactant–protein film undergoes triplet sensitized Z-to-E photoswitching upon far-red/red light excitation in air. The role of triplet sensitization in photoswitching has been confirmed by quenching of sensitizer phosphorescence by Z-Azo1 and temperature-dependent photoswitching experiments. Herein, we demonstrate new biosustainable fabrication designs to address key challenges in solid-state photoswitching, effectively mitigating chromophore aggregation and requirement of high energy excitations by dispersing the photoswitch in the trapped liquid inside the solid framework and by shifting the action spectrum from blue-green light (450–560 nm) to the far-red/red light (740/640 nm) region.

We report the first example of direct far-red endothermic triplet sensitized Z-to-E photoswitching of azobenzene derivative (Azo1) in a condensed phase of a liquid Azo1 co-assembled within a liquid surfactant-protein bioplastic film in air.     

PHOTOREACTIVATION OF ULTRAVIOLET LIGHT-INDUCED DAMAGE IN CULTURED FISH CELLS AS REVEALED BY INCREASED COLONY FORMING ABILITY AND DECREASED CONTENT OF PYRIMIDINE DIMERS

Abstract— Cultured cells derived from a goldfish were irradiated with 254nm ultraviolet light. Cell survival and splitting of pyrimidine dimers after photoreactivation treatment with white fluorescent lamps were examined by colony forming ability and by a direct dimer assay, respectively. When UV-irradiated (5 J/m²) cells were illuminated by photoreactivating light, cell survival was enhanced up to a factor of 9 (40min) followed by a decline after prolonged exposures. Exposure of UV-irradiated (15 J/m²) cells to radiation from white fluorescent lamps reduced the amounts of thymine-containing dimers in a photoreactivating fluence dependent manner, up to about 60% reduction at 120 min exposure. Keeping UV-irradiated cells in the dark for up to 120min did not affect either cell survival or the amount of pyrimidine dimers in DNA, indicating that there were not detectable levels of a dark-repair system in the cells under our conditions. Correlation between photoreactivation of colony forming ability and photoreactivation of the pyrimidine dimers was demonstrated, at least at relatively low fluences of photoreactivating light.     

Hydrogenation of carbon monoxide by tetranuclear rare earth metal polyhydrido complexes. Selective formation of ethylene and isolation of well-defined polyoxo rare earth metal clusters

The reaction of the tetranuclear rare earth metal polyhydrido complexes {Cp'Ln(mu-H)2}4(THF) (Cp' = C5Me4SiMe3, Ln = Y (1a), Lu (1b)) with carbon monoxide (1 atm) yielded ethylene and the corresponding tetraoxo cubane complexes (Cp'Ln)4(mu3-O)4 (Ln = Y (5a), Lu (5b)). Stepwise formation of some key reaction intermediates, such as oxymethylene complexes (Cp'Ln)4(mu-OCH2)(mu-H)6(THF) (Ln = Y (2a), Lu (2b)), enolate species (Cp'Y)4(OCH=CH2)(mu-O)(mu-H)5(THF) (3), and dioxo complex (Cp'Y)4(mu3-O)2(mu-H)4(THF) (4), was confirmed. The molecular structures of 2a, 4, and 5b were determined by X-ray diffraction studies.     

A one-pot synthesis of piperidinium spirooxindoline-pyridineolates and indole-substituted pyridones in aqueous or ethanol medium

Molecular Diversity - Piperidinium spirooxindoline-pyridineolate has been prepared via one-pot multicomponent reaction of isatin, malononitrile, cyanoacetohydrazide, and piperidine in water or...     

AUSM-like expression of HLLC and its all-speed extension

Advection upstream splitting method (AUSM) and Harten-Lax-van Leer with contact (HLLC) are two popular families of flux functions. The AUSM is simple and requires no eigenstructure, which facilitates its extensions to general equations of state. Furthermore, one of its variants, simple low-dissipation AUSM (SLAU), is applicable to all speeds and features removal of parameter setting by the user. HLLC, on the other hand, clearly defines three distinct waves in Riemann problem, namely, left-running and right-running acoustic waves, and entropy wave. This paper demonstrates that HLLC can be written in a very similar form with the AUSM family and that the similar manner in extending AUSM family to all speeds is easily incorporated into HLLC in this AUSM-like form. Then, we combine the strengths of the both flux functions and offer a new inviscid numerical flux function within the framework of monotone upwind scheme for conservation laws (MUSCL) in computational fluid dynamics (CFD) for Euler and Navier-Stokes equations. The resultant HLLC with low dissipation (HLLCL) numerical flux can compute low Mach number flows and sound propagations at the same time with high accuracy, as demonstrated by one-dimensional and two-dimensional numerical examples. Furthermore, the results indicate that its extensions to general fluids such as supercritical fluids are encouraging.     

Nonlinear acoustic response through minute surface cracks: FEM simulation and experimentation

The second harmonic of a Rayleigh wave passing through a minute surface crack has been numerically analyzed by semi-explicit FEM including special elements which account for a nonlinear stress-strain relation at crack surfaces. Minute cracks perpendicular to a free, flat surface close under compressive stress when width of the crack opening is less than the longitudinal amplitude of the Rayleigh wave. Thereafter, compressive and shear stresses are partially transmitted through the closed cracks, whereas tensile and shear stresses are not transmitted through cracks that remain open. This leads to marked nonlinear ultrasonic response. Calculation was performed for an aluminum block having a surface crack. The transverse component of the Rayleigh wave propagating through the cracks shows distorted waveforms, making the second harmonic amplitude clearly noticeable. In an experiment, the second harmonic component of the leaky Rayleigh wave was detected for a simple crack model consisting of two aluminum blocks, by use of a PVDF line-focused transducer. The results of the experiment show that the second harmonic amplitude is a second-order function of the fundamental wave amplitude, and is more pronounced for low compressive stress applied to close the crack surfaces.     

BINOL Aza Macrocycle Derivatives: Synthesis of Dinaphthosulfone Aza Macrocycles Using p-Toluenesulfonic Acid (p-TsOH) in Methanol as an Efficient Route and Evaluation of Their 1H NMR Spectra

Dinaphthosulfone aza macrocycles were synthesized from the reaction of diamines and dinaphthosulfone diester (1,1′-sulfoxobis-(2-naphthoxy(2-methyl acetate))) in methanol in the presence of catalytic amounts of para toluenesulfonic acid (p-TsOH). Dinaphthosulfone diester (1,1′-sulfoxobis-(2-naphthoxy(2-methyl acetate))) was synthesized from the corresponding dinaphthosulfide diester and hydrogen peroxide in formic acid at room temperature. Dinaphthosulfide diester was prepared from initial dinaphtholsulfide diol (1,1′-thio bis(2-hydroxy naphthalene)) and methylchloroacetate. ¹H NMR spectroscopy showed the unusual splittings for these dinaphthosulfone aza macrocycles, and this finding could be proposed as the role of tetrahedral structure of sulfone functional group, hydrogen bonding in the cavity and size of macrocycle.     

A Straightforward Method for the Synthesis of Functionalized Trisubstituted Alkenes through Na2S/Al2O3 Catalyzed Knoevenagel Condensation

Na₂S/Al₂O₃ catalyzed the Knoevenagel condensation between an aldehyde and an active methylene compound to yield various trisubstituted alkenes.     

Unique oxidative metal-metal bond formation of linearly aligned tetranuclear Rh-Mo-Mo-Rh clusters

Reaction of Mo2(pyphos)4 (1) with [RhCl(CO)2]2 followed by treatment of excess amounts of tBuNC resulted in the clean formation of [Mo2Rh2(tBuNC)4(pyphos)4](X)2 (4a; X = Cl). The X-ray diffraction study as well as spectroscopic analyses of 4c (X = BPh4) implied that there is no direct sigma-bonding interaction between each Rh(I) atom and the Mo2 core. Each Rh(I) atom in 4 can be oxidized concurrently by 2 equiv of [Cp2Fe]PF6 to afford [Mo2Rh2(Cl)2(tBuNC)4(pyphos)4](PF6)2 (5) along with the formation of two Mo-Rh(II) single bonds and the reduction of the bond orders of the Mo-Mo moiety.