New layered cobalt oxyfluoride, Sr2CoO3F

The first Ruddlesden-Popper type layered cobalt oxyfluoride, Sr(2)CoO(3)F, has been synthesized under a pressure of 6 GPa at 1700 °C and shown to adopt a K(2)NiF(4)-type structure with distorted square pyramidal coordination around Co and with O/F disorder at the apical sites.     

Low temperature solventless synthesis and characterization of Ni and Fe magnetic nanoparticles

We have successfully implemented a facile, one-pot solventless synthesis procedure starting from acetylacetonate salts and CaH(2) to obtain carbon-coated ferromagnetic metallic Ni and Fe nanoparticles at low temperature. The use of CaH(2) as a reductant drastically reduces reaction temperature down to 140 °C.     

Modular Design of Domain Assembly in Porous Coordination Polymer Crystals via Reactivity-Directed Crystallization Process

The mesoscale design of domain assembly is crucial for controlling the bulk properties of solids. Herein, we propose a modular design of domain assembly in porous coordination polymer crystals via exquisite control of the kinetics of the crystal formation process. Employing precursors of comparable chemical reactivity affords the preparation of homogeneous solid-solution type crystals. Employing precursors of distinct chemical reactivity affords the preparation of heterogeneous phase separated crystals. We have utilized this reactivity-directed crystallization process for the facile synthesis of mesoscale architecture which are either solid-solution or phase-separated type crystals. This approach can be also adapted to ternary phase-separated type crystals from one-pot reaction. Phase-separated type frameworks possess unique gas adsorption properties that are not observed in single-phasic compounds. The results shed light on the importance of crystal formation kinetics for control of mesoscale domains in order to create porous solids with unique cooperative functionality.     

Guest-to-host transmission of structural changes for stimuli-responsive adsorption property

We show that structural changes of a guest molecule can trigger structural transformations of a crystalline host framework. Azobenzene was introduced into a flexible porous coordination polymer (PCP), and cis/trans isomerizations of the guest azobenzene by light or heat successfully induced structural transformations of the host PCP in a reversible fashion. This guest-to-host structural transmission resulted in drastic changes in the gas adsorption property of the host-guest composite, displaying a new strategy for creating stimuli-responsive porous materials.     

Growth of single-crystal Ca10(Pt4As8)(Fe(1.8)Pt(0.2)As2)5 nanowhiskers with superconductivity up to 33 K

Single-crystal Ca(10)(Pt(4)As(8))(Fe(1.8)Pt(0.2)As(2))(5) superconducting (SC) nanowhiskers with widths down to hundreds of nanometers were successfully grown in a Ta capsule in an evacuated quartz tube by a flux method. Magnetic and electrical properties measurements demonstrate that the whiskers have excellent crystallinity with critical temperature of up to 33 K, upper critical field of 52.8 T, and critical current density of J(c) of 6.0 × 10(5) A/cm(2) (at 26 K). Since cuprate high-T(c) SC whiskers are fragile ceramics, the present intermetallic SC whiskers with high T(c) have better opportunities for device applications. Moreover, although the growth mechanism is not understood well, the technique can be potentially useful for growth of other whiskers containing toxic elements.     

Effect of the effective anisotropy field of soft layer on magnetic properties of soft/hard stacked media

Magnetic properties of soft/hard stacked perpendicular magnetic recording media were investigated using a two-moment model with taking account of demagnetizing energy. Demagnetizing energy of the soft layer may improve the uniformity of magnetic properties of the composite media and also decrease the interlayer thickness, although weaken the thermal stability a little. The application of high saturation magnetization (M_s) soft magnetic material as the soft layer may compensate for the undesirable contribution while maintaining its benefits.     

Study on magnetization reversal of cobalt nanowire arrays by magnetic force microscopy

The magnetic properties of self-assembly cobalt nanowire arrays formed in anodic porous alumina template were investigated by nanosize imaging method and macroscopic magnetic measurement. We have successfully made a wire-by-wire observation of magnetization reversal of a cobalt nanowire array using magnetic force microscopy with a home-made FePt tip. The nanowires in this medium have uniaxial anisotropy with easy axis along the wire due to the large aspect ratio of the wires (30 nm in diameter and 300 nm in length). Considering the nanowires as single-domain structures, we can obtain the average DC demagnetization curve from nanosize images by calculating the number of wires in each magnetized direction, and the results agreed well with the DC demagnetization curve measured by macroscopic measurement. The magnetostatic field between wires was evaluated by a new nanosize imaging method. Macroscopic measurement shows that reversible magnetization occurs in this medium. Nanosize images of the remanent and saturated states prove that the reversible magnetization processes mainly take place inside individual wires and reversed wires induced by magnetostatic field just give a little contribution to the reversible magnetization.     

Reactivity of a trivalent phosphorus radical cation as an electrophile toward pyridine derivatives

The reaction of methylviologen (MV²⁺) with tributylphosphine ( 1p ) and diethylphenylphosphine ( 1q ) in the presence of an alkyl-substituted pyridine ( 2 ) was found to take place through a single-electron transfer (SET) from 1 to MV²⁺ followed by nucleophilic attack by 2 on the resulting phosphine radical cation 1 ^•+. Kinetic examination showed that, in the transition state for the reaction of 1 ^•+ with 2 , an unpaired electron is largely delocalized to the pyridine moiety. © 2000 John Wiley & Sons, Inc. Heteroatom Chem 11:152–157, 2000