Helical gold nanotube synthesized at 150 K

Gold nanowires were synthesized at 150 K by electron beam thinning of a gold thin foil in an UHV electron microscope. The gold nanowires were found to have a helical multishell structure (HMS). One particular nanowire, which was thinner than the 7-1 HMS nanowire, was found to have a tubular structure. The gold single wall nanotube is composed of five atomic rows that coil about the tube axis. The diameter was 0.4 nm and the pitch was 11 nm. The stability of the (5,3) nanotube was discussed in terms of the shear deformation of the triangular network of gold atoms.     

Near-infrared emissions with widely different widths in two kinds of Er-doped oxide glasses with high refractive indices and low phonon energies

Er³⁺-doped alkali-barium-bismuth-tellurite (LKBBT) and alkali-barium-bismuth-gallate (LKBBG) glasses with high refractive indices and low phonon energies have been designed, fabricated, characterized and compared. Intense 1.53 μm emissions with widely different widths in the two kinds of glasses were observed and recorded under 980 nm diode laser excitation. The full-widths at half-maximum of the 1.53 μm emission bands in LKBBT and LKBBG glasses are 58 and 40 nm, and the lifetimes of them were measured to be 3.21 and 3.97 ms, respectively. The quantum efficiencies for the ⁴I_13/2 level in both glasses are almost 100%. The 1.53 μm broad and narrow emissions with high spontaneous emission probabilities and large emission cross-sections indicate that Er³⁺-doped LKBBT and LKBBG glasses are suitable materials in developing broadband optical amplifier and infrared laser, respectively.     

Application of Dithlol-s-triazine Derivatives to PVC CrossUnking

The effects of crosslinking on PVC are well known in regard to the improvement of mechanical properties, creep behavior, and softening temperature. Little is known, however, on the application of the PVC-crosslinking reaction, because most of crosslinked PVC tends to color easily at elevated temperatures. In this paper, a novel PVC-crosslinking reaction with 2-R-4,6-dithiol-s-triazine (I) has been presented to obtain insoluble products which hardly color on ageing. The reaction rate and induction period of the crosslinking reaction with I are made controllable by selecting the basicity of the substituent R of I as well as that of an acid acceptor in the blends. The utility of I as stabilizer as well as a crosslinking agent is also emphasized.     

Selective synthesis of poly(p‐oxybenzoyl) by fractional polycondensation: Enhancement of selectivity by shearing

The influence of shear flow, especially the timing for the application of shearing, was examined to enhance the selectivity for the preparation of poly(p‐oxybenzoyl) (Pp‐OB) by using hydrodynamically induced phase separation during polymerization of 4‐(4‐acetoxybenzoyloxy)benzoic acid (p‐ABAD) and m‐acetoxybenzoic acid (m‐ABA). The polymers containing few m‐oxybenzoyl (m‐OB) moieties were obtained as precipitates even at high content of m‐OB moiety in feed (χ_f) under shear flow. The content of m‐OB moiety in the precipitates (χ_p) prepared under shearing throughout the polymerization at the shear rate (γ) of 489 s^?1 was 6.3 mol % even at χ_f of 60 mol %. Especially, the Pp‐OB was obtained as the precipitates at χ_f of less than 50 mol %. The timing of the application of the shearing influenced the selectivity significantly, and the shearing just after the precipitation of the oligomers started was quite efficient to enhance the selectivity more. The χ_p of the precipitates prepared with shearing at γ of 489 s^?1 just after the precipitation was only 3.9 mol % even at χ_f of 60 mol %. The shear flow reduced the difference in the reactivity between p‐ABAD and m‐ABA, resulting in the decrease in the selectivity with regard to the formation of p‐oxybenzoyl homo‐oligomer. However, the shear flow enhanced the difference in the miscibility between homo‐oligomers and co‐oligomers. This change in the miscibility by shear flow brought about the more rapid precipitation of homo‐oligomers, leading to the enhancement of the selectivity. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

Preparation of poly(p‐oxybenzoyl) crystals using direct polymerization of p‐hydroxybenzoic acid in the presence of boronic anhydrides

Poly(p‐oxybenzoyl) (POB) crystals were prepared by reaction‐induced crystallization during direct polymerization of p‐hydroxybenzoic acid in the presence of boronic anhydrides. Polymerizations were carried out at 300 °C in dibenzyltoluene at a concentration of 1% with three kinds of anhydrides of boronic acid such as 3,4,5‐trifluorophenylboronic acid (TFB), 4‐methoxyphenylboronic acid (MPB) and 4‐biphenylboronic acid (BPB). The POB crystals were formed as precipitates in the solution and the morphology was considerably influenced by both the structure of the boronic anhydride and its concentration (c_B). Needle‐like crystals were firmed in the presence of TFB anhydride (TFBA) at c_Bs of 5 and 10 mol % by the spiral growth of lamellae. Spherical aggregates of slab‐like crystals were formed at c_Bs from 50 to 100 mol %. The polymerization with MPB anhydride and BPB anhydride (BPBA) also yielded the needle‐like crystals at c_Bs of 50 and 5 mol %, respectively. The polymerization with TFBA at lower c_B was favorable to prepare the needle‐like crystal. Molecular weight was also influenced by the structure of the boronic anhydride and c_B. M_n increased generally with c_B and BPBA gave the highest M_n of 14.7 × 10³ at c_B of 100 mol %. The loose packing of the molecules in the crystal caused by the bulkiness of the end‐groups made the polymerization in the crystals more efficiently. Morphology and molecular weight of the POB crystals could be controlled by the chemical structure and the content of boronic anhydride. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011.     

Anomalous thermochromic transition of poly(di‐n‐octylsilane)

The thermochromic behavior of poly(di‐n‐octylsilane) {[Si(C₈H₁₇)₂]_n; PDOS} was studied by ultraviolet (UV) absorption, differential scanning calorimetry, and X‐ray diffraction measurements. The structure of PDOS in the low‐temperature phase strongly depended on not only the temperature but also the rate of cooling, that is, the thermal history. Temperature‐dependent UV absorption spectra were highly dependent on thermal hysteresis. Cooled rapidly (10 K/min), PDOS showed two absorption peaks at 3.32 and 3.51 eV in low‐temperature‐ordered phases, whereas a single absorption peak at 3.32 eV became predominant with slow cooling (0.3 K/min). The appearance of the two peaks at low temperatures suggested that a mixture of different conformations was introduced by rapid cooling. A fiber diffraction pattern measured at 240 K after rapid cooling also showed evidence of the existence of novel conformation. A temperature‐dependent powder X‐ray diffraction pattern changed significantly between 270 and 280 K. Rapid cooling reduced the intensity of the X‐ray diffraction peak in this temperature region. This intensity change was explained by the conformational mixture in the polymer. © 2001 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 39: 1085–1092, 2001     

Preparation of open tubular solid-phase extraction column with 5-amino-8-hydroxyquinoline-modified gold nanoparticle phase for the enrichment of heavy metal ions.

A 5-amino-8-hydroxyquinoline (AHQ)-modified gold nanoparticle (GNP) layer was fabricated on an inner wall of a silica capillary column by alternatively passing a citrate-stabilized GNP solution and an AHQ solution in a repeating fashion. The observations by a field emission scanning electron microscope showed that the thickness of the resulting GNP layer was about 0.15 microm. This column was then used as an open tubular solid-phase extraction column for cadmium, followed by electrothermal atomic absorption spectrometric determination. The detection limit of 0.009 ng ml(-1) was obtained.     

Positive Galois coverings of self-injective algebras

In the article, we study the structure of Galois coverings of self-injective artin algebras with infinite cyclic Galois groups. In particular, we characterize all basic, connected, self-injective artin algebras having Galois coverings by the repetitive algebras of basic connected artin algebras and with the Galois groups generated by positive automorphisms of the repetitive algebras.