Calculating the surface tension between a flat solid and a liquid: a theoretical and computer simulation study of three topologically different methods

We discuss three topologically different methods for calculating the surface tension between a flat solid and a liquid from theoretical and computer simulation viewpoints. The first method, commonly used in experiments, measures the contact angle at which a static droplet of liquid rests on a solid surface. We present a new analysis algorithm for this method and explore the effects of line tension on the contact angle. The second method, commonly used computer simulations, uses the pressure tensor through the virial in a system where a thick, infinitely extended slab of liquid rests on a solid surface. The third method, which is original to this paper and is closest to the thermodynamic definition of surface tension, applies to a spherical solid in contact with liquid in which the flat solid is recovered by extrapolating the sphere radius to infinity. We find that the second and third methods agree with each other, while the first method systematically underestimates surface tension values.     

Diastereoselective syntheses and oxygenation of silyl fulleroids

The addition of silyl diazomethane (1a-d) to fullerene C₆₀ at room temperature provided the mono-adducts, the bis- and tris-adducts of silyl fulleroid (3a-d) in moderate yields. The structures of the silyl fulleroids were characterized by mass spectroscopy, as well as ¹H and ¹³C NMR. The gated ¹H NMR and ¹³C-¹H COLOC analyses of 3a-d showed a correlation between the methine proton resonances and three fullerene carbons. These observations, as well as the ¹H NMR chemical shifts of the methine protons, suggest a remarkable diastereoselectivity, with the silyl groups located above a five-membered ring. Two transition states of the thermal nitrogen-extrusion of pyrazoline intermediate (2a) were theoretically obtained, the structures of which disclosed that the diastereoselectivity is a consequence of minimization of the repulsive interaction between the silyl groups and the N₂ moiety. The bridgehead CC double bond of the silyl fulleroid is thought to be reactive by POAV analyses. The silyl fulleroids (3a,b) were found to react with singlet oxygen to afford the silyl enol ether (9a,b) via 1,3-silyl migration of a diketone (8a,b). This is the first example of ¹O₂ oxygenation of fulleroids.     

High oxygen-reduction activity of silk-derived activated carbon

Activated carbon prepared from silk fibroin, which is free of metal elements, showed a high catalytic activity for the oxygen-reduction reaction (ORR). The activated carbon had a very high onset potential of E_onset = 0.83 V (vs. RHE) in oxygen-saturated 0.5 M H₂SO₄ at 60 °C. The ORR on the activated carbon proceeded by a four-electron process in the high-electrode-potential region; this gradually decreased to a 3.5-electron reaction below about 0.6 V (vs. RHE). Only about 1% of nitrogen atoms (mostly quaternary) remained in the activated carbon by heat-treatment at up to 1200 °C are responsible for the high catalytic activity. The open circuit voltage of a polymer electrolyte fuel cell using the activated carbon as the cathode and a platinum/carbon black anode under pure oxygen and hydrogen gases, respectively, both at one atmosphere, was 0.96 V at 27 °C.     

Planar catechin analogues with alkyl side chains: a potent antioxidant and an alpha-glucosidase inhibitor

Planar catechin analogues having various alkyl side chain lengths were synthesized, and their remarkable antioxidative abilities and alpha-glucosidase inhibitory activities are shown.     

X-ray illumination induced Fe(II) spin crossover in the Prussian blue analogue cesium iron hexacyanochromate

The effect of X-ray illumination on the structural properties of the mixed valence Prussian blue analogue CsFe(II)[Cr(III)(CN)6] has been studied by time-dependent high-resolution synchrotron X-ray diffraction. Abrupt isosymmetric phase transitions, accompanied by dramatic volume collapse, were found in the temperature range 245-265 K, induced by sudden Fe(II) spin transitions from the high spin (HS) (4t(2g)2e(g), S = 2) to the low spin (LS) (6t(2g)0e(g), S = 0) configuration. Absorption of X-ray photons generates photoexcited Fe(II)(LS) domains whose size rapidly grows with time until the percolation threshold is reached and the structure collapse is triggered. The persistent character of the optically excited spin crossover states derives from the strong electron-phonon coupling, associated with the large lattice relaxations, which accompany the internal spin rearrangements. It is thus possible to use X-ray light in a controllable and efficient way to induce photoswitching between the ground and hidden or inaccessible excited states in suitably selected multistable materials in the bulk.     

Interrelation between inhomogeneity and cyclability in O3‐NaFe1/2Co1/2O2

O3‐NaFe_1/2Co_1/2O₂ shows initial capacity of 160 mAh/g and an average operating voltage of 3.1 V (vs. Na) with good cyclability, and is a promising candidate of the cathode materials for sodium‐ion secondary batteries (SIBs). Here, we found that the cyclability of the slowly‐cooled sample is much worse than that of quenched one, even though the former sample keeps the O3‐type structure. The energy dispersive X‐ray spectroscopy (EDX) images suggest that the slow‐cooled sample (Na_x Fe_1–yCo_y O₂) is inhomogeneous in the Fe concentration (1 – y), perhaps triggered by the Na deficiency (1 – x). We ascribed the poor cyclability in the slowly‐cooled sample to the concentration inhomogeneity (Δy). The Δy is further responsible for the fluctuation of the lattice constants (a and c), as revealed by the Williamson–Hall plot. (© 2016 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim)     

Visualization of high-order dispersion for compression of few-cycle pulses

We present a visually intuitive method for higher-order dispersion compensation based on multi-photon interpulse interference pulse scans. The dispersion values obtained from these scans are fed back as a correction to an acousto-optical programmable dispersive filter to compensate residual higher-order dispersions up to fifth order. This method is applied to the dispersion management of a non-collinear optical parametric chirped-pulse amplifier. A grism-pair stretcher is designed based on a global dispersion balance which provides a large stretching factor and supports a spectral bandwidth of up to 320 nm. It is implemented in a two-stage three-pass non-collinear optical parametric chirped-pulse amplifier and stretches 6-fs seed pulses to about 80 ps from 700 to 1,000 nm. The amplified pulses are compressed by material dispersion. Pulses of less than 10-fs duration with a pulse energy of 125 μJ are obtained at 20-kHz repetition rate.     

Intramolecular σ-bond metathesis between carbon-carbon and silicon-silicon bonds

An intramolecular σ-bond metathesis between carbon-carbon and silicon-silicon bonds took place on treatment of a disilane tethered to a cyclobutanone with a palladium(0) catalyst, furnishing a silaindane skeleton as well as an acylsilane functionality at once.     

Organotin-catalyzed highly regioselective thiocarbonylation of nonprotected carbohydrates and synthesis of deoxy carbohydrates in a minimum number of steps

Nonprotected carbohydrates: The catalytic regioselective thiocarbonylation of carbohydrates by using organotin dichloride under mild conditions was demonstrated. The reaction afforded various deoxy saccharides in high yields and excellent regioselectivity in a minimum number of steps. The regioselectivity of the thiocarbonylation is attributed to the intrinsic character of the carbohydrates based on the stereorelationship of their hydroxy groups (see scheme).