ELECTRIC DICHROISM OF PURPLE MEMBRANE SUSPENSIONS

Abstract— Suspensions of purple membranes were exposed to reversing rectangular pulses of relatively low electric field (less than 100V/cm) at various frequencies. Orientation of the membranes was estimated by measuring linear dichroism at 565nm. In the electric field of frequency lower than about 10Hz the purple membranes tended to align perpendicular to the electric field. This orientation was induced mostly by permanent dipole which was perpendicular to the membrane surface. The value of permanent dipole moment was determined to be 140D per protein at pH 7.0, 25°C, in the presence of 5m M phosphate buffer.
In an electric field of frequency more than 100Hz the membrane tended to align parallel to the electric field. Electric polarizability parallel to the membrane surface was estimated to be 1 ± 10⁻¹² cm³ under the same conditions.
Electric dichroism of light-adapted and dark-adapted purple membranes was found to coincide with each other at high frequency. From this result the angle of retinal to the membrane surface was concluded to be the same between light-adapted and dark-adapted bacteriorhodopsins.     

Extra‐Large Mechanical Anisotropy of a Hydrogel with Maximized Electrostatic Repulsion between Cofacially Aligned 2D Electrolytes

In our previous work, we have shown that “electrostatic forces”, when generated anisotropically in aqueous media by 2D electrolytes upon cofacial orientation, enable the formation of a hydrogel with an anisotropic parameter, as defined by the ratio of elastic moduli E_⊥/E_∥, of 3.0. Herein, we successfully developed the design strategy for a hydrogel with an anisotropic parameter of no less than 85. This value is not only 28 times greater than that of our previous anisotropic hydrogel but also 6 times larger than the current champion record in synthetic hydrogels (E_⊥/E_∥～15). Firstly, we simply lowered ionic contaminants in the hydrogel and were able to enhance the anisotropic parameter from 3.0 to 18. Then, we chose a supporting polymer network allowing the hydrogel to carry a higher interior permittivity. Consequently, the anisotropic parameter was further enhanced from 18 to 85. Owing to the enhanced mechanical anisotropy, our new hydrogel displayed a superb ability of seismic isolation.     

A new synthesis of d1-coriolin A. Application of a new SN2 reaction at a neopentylic position

Dicyclopentadiene has been stereoselectively converted to a key tricyclic intermediate for the total synthesis of coriolin, through a route which involves a new S_N2 reaction at a neopentylic position.     

Effect of graft copolymer on demixing of immiscible polymers in solution

The effect of graft copolymer on the demixing of solutions of two immiscible homopolymers and critical conditions for emulsion formation were studied. The graft copolymer used in the present work consists of one backbone poly(vinyl acetate) (PVAc) and one branch polystyrene (PS). PVAc and PS of various degrees of polymerization were used as immiscible homopolymers. The common solvent was benzene. When the concentration of homopolymer blend was not sufficiently higher than the critical concentration for demixing of the blend solution, no stable emulsion was formed, even when a considerable amount of graft copolymer was present, and the added graft copolymer merely reduced the demixing rate. However, as the blend concentration was increased, a stable emulsion could readily be obtained by addition of rather small amounts of graft copolymer. The radius of emulsion droplets was inversely proportional to the weight ratio of the graft copolymer to the dispersed component polymer, in accordance with the theoretical prediction. It was concluded that the emulsions were stabilized against coagulation by graft copolymer molecules fixed strongly as a monolayer on the interface of the emulsion.     

Spin-dependent tunneling and Coulomb blockade in ferromagnetic nanoparticles

In this paper we review studies on spin-dependent transport in systems containing ferromagnetic nanoparticles. In a tunnel junction with a nanometer-scale-island, the charging effect leads to an electric current blockade phenomenon in which a single electron charge plays a significant role in electron transport, resulting in single-electron tunneling (SET) properties such as Coulomb blockade and Coulomb staircase. In a tunnel junction with a ferromagnetic nano-island and electrode, it was expected that the interplay of spin-dependent tunneling (SDT) and SET, i.e., spin-dependent single-electron tunneling (SD-SET), would give rise to remarkable tunnel magnetoresistance (TMR) phenomena. We investigated magnetotransport properties in both sequential tunneling and cotunneling regimes of SET and found the enhancement and oscillation of TMR. The self-assembled ferromagnetic nanoparticles we have employed in this study consisted of a Co–Al–O granular film with cobalt nanoparticles embedded in an Al–O insulating matrix. A _Co36Al22O42${\mathrm{Co}}_{36}{\mathrm{Al}}_{22}{\mathrm{O}}_{42}$ film prepared by a reactive sputtering method produced a TMR ratio reaching 10% and superparamagnetic behavior at room temperature. The TMR ratio exhibited an anomalous increase at low temperatures but no indication of change with bias voltage. In Section 4, we show that the anomalous increase of the MR provided evidence for higher-order tunneling (cotunneling) between large granules through intervening small granules. We emphasize that the existence of higher-order tunneling is a natural consequence of the granular structure, since broad distribution of granule size is an intrinsic property of granular systems. In Section 5, we concentrate on SD-SET properties in sequential tunneling regimes. We fabricated two types of device structures with Co–Al–O film using focused ion-beam milling or electron-beam lithography techniques. One had a granular nanobridge structure: point-shaped electrodes separated by a very narrow lateral gap filled with the Co–Al–O granular film. The other had a current-perpendicular-to-plane (CPP) geometry structure: a thin Co–Al–O granular film sandwiched by ferromagnetic electrodes with the current flowing in the direction perpendicular to the film plane through a few Co particles. We found the enhancement and oscillation of TMR due to spin-dependent SET in sequential tunneling regimes. In Section 6, we report experimental evidence of a spin accumulation effect in Co nanoparticles leading to the oscillation of TMR with alternate sign changes. Furthermore, we discovered that the spin relaxation time in the nanoparticles is unprecedentedly enhanced up to the order of more than hundreds of nanoseconds, compared to that evaluated from the spin-diffusion length of ferromagnetic layers in previous CPP-GMR studies, i.e., the order of tens of picoseconds.     

Synthesis and Bowl-in-Bowl Assembly of a Geodesic Phenylene Bowl

A phenylene multiring with a corannulenoidal skeleton was synthesized. Geodesic constraints over 20 phenylene panels resulted in its nanometer-sized, bowl-shaped molecular structure, which was unequivocally revealed by crystallographic analysis. The crystal structure also showed the presence of a bowl-in-bowl dimeric assembly, which was driven by entropic factors in solution.     

Control of thermal,mechanical, and optical properties of three‐component maleimide copolymers by steric bulkiness and hydrogen bonding

N‐substituted maleimides polymerize in the presence of a radical initiator to give polymers with excellent thermal stabilities and transparency. In this study, we synthesized various maleimide copolymers with styrenes and acrylic monomers to control their thermal and mechanical properties by the introduction of bulky substituents and intermolecular hydrogen bonding. Three‐component copolymers of N‐(2‐ethylhexyl)maleimide in combination with styrene, α‐methylstyrene (MSt), or 1‐methylenebenzocyclopentane (BC5) as the styrene derivatives, and n‐butyl acrylate, 2‐hydroxyethyl acrylate, 4‐hydroxybutyl acrylate, or acrylic acid as the acrylic monomers were prepared by radical copolymerization. These copolymers were revealed to exhibit excellent heat resistance by thermogravimetric analysis. Glass transition temperatures increased by the introduction of bulky MSt and BC5 repeating units. The mechanical properties of the copolymer films were improved by the introduction of intermolecular hydrogen bonding. Optical properties, such as transmittance, refractive index, Abbe number, and birefringence, were determined for the copolymers. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 1569–1579     

One-Step Preparation of Fe/N/C Single-Atom Catalysts Containing Fe−N4 Sites from an Iron Complex Precursor with 5,6,7,8-Tetraphenyl-1,12-Diazatriphenylene Ligands

Fe/N/C single-atom catalysts containing Fe−N_x sites prepared by pyrolysis are promising cathode materials for fuel cells and metal-air batteries due to their high oxygen reduction reaction (ORR) activities. We have developed iron complexes containing N2- or N3-chelating coordination structures with preorganized aromatic rings in a 1,12-diazatriphenylene framework tethering bromo substituents as precursors to precisely construct Fe−N₄ sites in an Fe/N/C catalyst. One-step pyrolysis of the iron complex with carbon black forms atomically dispersed Fe−N₄ sites without iron aggregates. X-ray absorption spectroscopy (XAS) and electrochemical measurements revealed that the iron complex with N3-coordination is more effectively converted to Fe−N₄ sites catalyzing ORR with a TOF value of 0.21 e site⁻¹ s⁻¹ at 0.8 V vs. RHE. This indicates that the formation of Fe−N₄ sites is controlled by precise tuning of the chemical structure of the iron complex precursor.