Layer-by-layer assembly of charged poly(phenylacetylene)s with induced macromolecular helicity

The macromolecular helicity of charged poly(phenylacetylene)s induced by small chiral guests in water can be retained by the alternative deposition of achiral polyelectrolytes with opposite charges, resulting in optically active multilayer thin films with a macromolecular helicity memory.     

Synthesis and properties of naphthalene trimers linked by 1,3,4-oxadiazole spacers

Two types of naphthalene trimers linked by 1,3,4-oxadiazole spacers were synthesized and investigated for their physical and electronic properties. 2,6- and 2,7-isomers on central naphthalene moieties were obtained in the forms of pale yellow solids and colorless crystals, respectively. The melting point of the 2,6-isomer was higher than that of the 2,7-isomer. An X-ray crystallographic analysis revealed a π-stacked column with a short intermolecular distance in the crystals of the 2,6-isomer. The absorption maximum of the 2,6-isomer was red-shifted as compared to that of the 2,7-isomer, indicating a π-conjugation between di-2-naphthyloxadiazole moieties in the 2,6-isomer. The quantum yields of the 2,6- and 2,7-isomers were measured to be 0.97 and 0.74, relative to that of 2,5-di-2-naphthyl-1,3,4-oxadiazole (0.85). Molecular orbital (MO) calculations demonstrated that the 2,6-isomer had a higher electron affinity than the 2,7-isomer. Thus, the crosslinking of building blocks is important for the design of functional materials.     

Optimization of ETV-ICP-MS conditions for the determination of multi-elements in semiconductor grade acids

The performance of an electro thermal vaporization (ETV) unit as a sample introduction device for an inductively coupled plasma mass spectrometer (quadrupole-ICP-MS) was evaluated. The technique was found to have several advantages over the conventional nebulization method. Some features of ETV-ICP-MS for single element determination have been investigated. Attempts were made to optimize the experimental parameters such as vaporization temperature, vaporization interval and carrier gas flow rate. The study highlights on the determination of Cr, Mn, Al and Na. A compromise condition for multi-element determination was suggested and tested from single-element optimum conditions obtained. 25 L solution was used for the analysis. Results obtained for the analysis of conc. HCl samples are also reported.     

Chemically amplified kojic acid responses of tyrosinase-based biosensor, based on inhibitory effect to substrate recycling driven by tyrosinase and -ascorbic acid

A tyrosinase-based chemically amplified biosensor, based on the substrate recycling of polyphenols driven by tyrosinase-catalyzed oxidation and chemical reduction by -ascorbic acid (AsA), has been utilized for the highly sensitive detection of inhibitors of tyrosinase such as kojic acid, benzoic and SCN⁻ ion. The amplified current response of immobilized tyrosinase-coupling oxygen electrode due to the recycling was suppressed by the addition of inhibitors, and a highly amplified response to kojic acid over other inhibitors was observed in the presence of 5 mM AsA. The amplification factor (AF) of kojic acid is substantially proportional to the AF of substrates, and the AF for 1 × 10⁻⁷ M kojic acid was increased by up to a factor of 143 when 1 × 10⁻⁵ M dopamine was used as a competitive substrate in the presence of 5 mM AsA. The amplified calibration curve of kojic acid obtained with 5 mM AsA was shifted towards more than a two decades lower concentration range compared with that of the non-amplified response, and the detection limit of kojic acid was lowered to 7 × 10⁻⁸ M.     

Helical arrays of pendant fullerenes on optically active poly(phenylacetylene)s

Novel, optically active, stereoregular poly(phenylacetylene)s bearing the bulky fullerene as the pendant were synthesized by copolymerization of an achiral phenylacetylene bearing a [60]fullerene unit with optically active phenylacetylene components in the presence of a rhodium catalyst. The C60-bound phenylacetylene was prepared by treatment of C60 with N-(4-ethynylbenzyl)glycine in a Prato reaction. The obtained copolymers exhibited induced circular dichroism (ICD) in solution both in the main-chain region and in the achiral fullerene chromophoric region, although their ICD intensities were highly dependent on the structures of the optically active phenylacetylenes and the solution temperature. These results indicate that the optically active copolymers form one-handed helical structures and that the pendant achiral fullerene groups are arranged in helical arrays with a predominant screw sense along the polymer backbone. The structures and morphology of the copolymers on solid substrates were also investigated by atomic force microscopy.     

Structural Design of Ionic Conduction Paths in Molecular Crystals for Selective and Enhanced Lithium Ion Conduction

The molecular crystals [Li{N(SO₂CF₃)₂}{C₆H₄(OCH₃)₂}₂] and [Li{N(SO₂CF₃)₂}{C₆F₂H₂(OCH₃)₂}₂] with solid‐state lithium ion conductivity have been synthesized by the addition of two equivalents of 1,2‐dimethoxybenzene or 1,2‐difluoro‐4,5‐dimethoxybenzene to Li{N(SO₂CF₃)₂}, respectively. Single‐crystal X‐ray diffraction analysis revealed the formation of ionic conduction paths with an ordered arrangement of lithium ions in these crystal structures, afforded by the self‐ assembled stacking of molecular‐based channels consisting of N(SO₂CF₃)₂ anion and 1,2‐dimethoxybenzene frameworks as a result of intermolecular aromatic and hydrogen interactions. These compounds show selective lithium ion conductivity as the anions behave as a component unit of the conduction paths. The relationship between the crystal structure and ionic conductivity of the molecular crystals provides a clue to the development of novel solid electrolytes based on molecular crystals showing fast and selective lithium ion conduction.     

Current driven domain wall velocities exceeding the spin angular momentum transfer rate in permalloy nanowires

The velocity of domain walls driven by current in zero magnetic field is measured in permalloy nanowires using real-time resistance measurements. The domain wall velocity increases with increasing current density, reaching a maximum velocity of approximately 110 m/s when the current density in the nanowire reaches approximately 1.5 x 10(8) A/cm(2). Such high current driven domain wall velocities exceed the estimated rate at which spin angular momentum is transferred to the domain wall from the flow of spin polarized conduction electrons, suggesting that other driving mechanisms, such as linear momentum transfer, need to be taken into account.     

Macromolecular helicity inversion of poly(phenylacetylene) derivatives induced by various external stimuli

Unique macromolecular helicity inversion of stereoregular, optically active poly(phenylacetylene) derivatives induced by external achiral and chiral stimuli is briefly reviewed. Stereoregular, cis-transoidal poly(phenylacetylene)s bearing an optically active substituent, such as (1R,2S)-norephedrine (poly- 1 ) and β-cyclodextrin residues (poly- 2 ), show an induced circular dichroism (ICD) in the UV-visible region of the polymer backbone in solution due to a predominantly one-handed helical conformation of the polymers. However, poly- 1 undergoes a helix-helix transition upon complexation with chiral acids having an R configuration, and the complexes exhibit a dramatic change in the ICD of poly- 1 . Poly- 2 also shows the inversion of macromolecular helicity responding to molecular and chiral recognition events that occurred at the remote cyclodextrin residues from the polymer backbone; the helicity inversion is accompanied by a visible color change. A similar helix-helix transition of poly((R)- or (S)-(4-((1-(1-naphthyl)ethyl)carbamoyl)phenyl)acetylene) is also briefly described.