Selective synthesis of organogold magic clusters Au54(C≡CPh)26

Organogold clusters Au(54)(C(2)Ph)(26) were selectively synthesized by reacting polymer-stabilized Au clusters (1.2 ± 0.2 nm) with excess phenylacetylene in chloroform.     

Cu NMR/NQR Studies on Magnetism in Impurity/Hole-Doped Spin-Ladder Compounds

Cu nuclear magnetic resonance (NMR) spectra of impurities (Zn, Ni, and La)-doped spin-1/2 Heisenberg ladder compounds SrCu₂O₃ (Sr123) are broadened with Curie-like temperature (T) dependence. The spectra have been successfully fit by using a quasi-one-dimensional (Q1D) staggered polarization (SP) model. Such a SP has also revealed in Cu NMR measurements of Sr_14–x Ca _x Cu₂₄O₄₁ (Cax) with hole-doped ladders. The origin of possible 3D antiferromagnetic (AF) long-range ordering in (Zn and Ni)-doped Sr123 and Cax around x=12 at low T is considered to be similar. Once unpaired spins S ₀'s are induced and 3D interlayer interaction occurs, the localized spins couple in the whole system.     

Appearance of magnetic long range order in the spin ladder compound LaCuO2.5

We report here the two current topics in the ladder compounds. 1. The new ladder compound LaCuO_2.5 recently discovered by Hiroi and Takano shows a clear sign of magnetic long range order at around 125 K observed by μ⁺SR technique. This result demonstrates that the ground state of LaCuO_2.5 is not a spin liquid state, but a magnetically ordered state. 2. Superconductivity has been found in the ladder material (Sr,Ca)₁₄Cu₂₄O₄₁ under high pressure between 3 GPa and 4.5 GPa. The superconducting transition temperatures T_c (onset) are 12 K and 9 K at 3 GPa and 4.5 GPa, respectively. This revised version was published online in July 2006 with corrections to the Cover Date.     

Magnetic properties of hexagonal ferrite dot arrays

Patterned magnetic media have been considered as one of the promising candidates for future ultra-high-density magnetic recording. In this paper, a new kind of patterned medium based on hexagonal ferrite have been studied. We have successfully fabricated strontium ferrite dot arrays by electron beam lithography. Their magnetic properties are evaluated by magnetic force microscopy (MFM) and superconducting quantum interference device (SQUID). The results show the dot arrays have perpendicular anisotropy. Dots with the lateral size larger than 500 nm show multidomain magnetization configuration in the initial magnetization state. However, with dot size decreased to 500 nm, all the dots have single-domain configuration both in the initial magnetization state and remanent magnetization state.     

Predissociation of acetylene in à Au state

The fluorescence excitation spectrum, the MPI spectrum, and the absorption spectrum of acetylene due to the à ¹A_u← transition were observed in a gas and in a supersonic jet. A sudden decrease in the fluorescence quantum yield Φ_f was found above the V⁴ K² (46339 cm⁻¹) vibronic sublevel. The decrease is due to predissociation into C₂H + H. AK and J dependence on Φ_f was also found.     

Design of base-discriminating fluorescent nucleoside and its application to t/c SNP typing

We report a novel method for base detection using a base-discriminating fluorescent (BDF) nucleoside. We developed BDF probes containing methoxybenzodeazaadenine MDA and methoxybenzodeazainosine MDI, which give strong fluorescence only when the base on the complementary strand is cytosine and thymine, respectively. Thus, the MDA- and MDI-containing ODNs can be used as a very effective BDF probe for the detection of single base alterations, such as SNPs and point mutations. The present method using BDF probes is a very powerful tool for SNP typing that does not require any enzymes and time-consuming steps, and can avoid hybridization errors. In addition, a combination of MDA- and MDI-containing BDF probes facilitates the T/C SNP typing of a heterozygous sample.     

Overcoming Steric Hindrance in Aryl-Aryl Homocoupling via On-Surface Copolymerization

On-surface synthesis is a unique tool for growing low-dimensional carbon nanomaterials with precise structural control down to the atomic level. This novel approach relies on carefully designed precursor molecules, which are deposited on suitable substrates and activated to ultimately form the desired nanostructures. One of the most applied reactions to covalently interlink molecular precursors is dehalogenative aryl-aryl coupling. Despite the versatility of this approach, many unsuccessful attempts are also known, most of them associated to the poor capability of the activated precursors to couple to each other. Such failure is often related to the steric hindrance between reactants, which may arise due to their coplanarity upon adsorption on a surface. Here, we propose a copolymerization approach to overcome the limitations that prevent intermolecular homocoupling. We apply the strategy of using suitable linkers as additional reactants to the formation of fully conjugated polycyclic nanowires incorporating non-benzenoid rings.