Organic Chemistry By Dr. I. L. Finar. Vol. 2: Stereochemistry and the Chemistry of Natural Products. Pp. xi + 733. (London and New York: Longmans, Green and Co., Ltd., 1956.) 40s. net.

Advanced Organic Chemistry

A simple hydrothermal method has been developed for the systematic synthesis of lanthanide orthophosphate crystals with different crystalline phases and morphologies. It has been shown that pure LnPO4 compounds change structure with decreasing Ln ionic radius:  i.e., the orthophosphates from Ho to Lu as well as Y exist only in the tetragonal zircon (xenotime) structure, while the orthophosphates from La to Dy exist in the hexagonal structure under hydrothermal treatment. The obtained hexagonal structured lanthanide orthophosphate LnPO4 (Ln = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, and Dy) products have a wirelike morphology. In contrast, tetragonal LnPO4 (Ln = Ho, Er, Tm, Yb, Lu, Y) samples prepared under the same experimental conditions consist of nanoparticles. The obtained hexagonal LnPO4 (Ln = La → Tb) can convert to the monoclinic monazite structured products, and their morphologies remained the same after calcination at 900 °C in air (Hexagonal DyPO4 is an exceptional case, it transformed to tetragonal DyPO...

Systematic synthesis and characterization of single-crystal lanthanide orthophosphate nanowires.

Herein, we present a survey of the literature covering the development of molecular imprinting science and technology over the years 2004-2011. In total, 3779 references to the original papers, rev ...

Molecular imprinting science and technology: a survey of the literature for the years 2004-2011.

Boronate affinity materials, as unique sorbents, have emerged as important media for the selective separation and molecular recognition of cis-diol-containing compounds. With the introduction of boronic acid functionality, boronate affinity materials exhibit several significant advantages, including broad-spectrum selectivity, reversible covalent binding, pH-controlled capture/release, fast association/desorption kinetics, and good compatibility with mass spectrometry. Because cis-diol-containing biomolecules, including nucleosides, saccharides, glycans, glycoproteins and so on, are the important targets in current research frontiers such as metabolomics, glycomics and proteomics, boronate affinity materials have gained rapid development and found increasing applications in the last decade. In this review, we critically survey recent advances in boronate affinity materials. We focus on fundamental considerations as well as important progress and new boronate affinity materials reported in the last decade. We particularly discuss on the effects of the structure of boronate ligands and supporting materials on the properties of boronate affinity materials, such as binding pH, affinity, selectivity, binding capacity, tolerance for interference and so on. A variety of promising applications, including affinity separation, proteomics, metabolomics, disease diagnostics and aptamer selection, are introduced with main emphasis on how boronate affinity materials can solve the issues in the applications and what merits boronate affinity materials can provide.

Boronate affinity materials for separation and molecular recognition: structure, properties and applications

Metal ion-imprinted polymers : Novel materials for selective recognition of inorganics

Various rare earth phosphates [rare earth elements: R = La, Ce, Pr, Nd, Sm, Yb, and Y; phosphates: Monazite-type, Xenotime-type, Rhabdophane-type, and Weinshenkite-type orthophosphates RPO4, polyphosphate R(PO3)3, and ultraphosphate RP5O14] were synthesized by heating the mixtures of each rare earth oxide and diammonium hydrogenphosphate or phosphoric acid. The compositions of rare earth phosphates were determined by XRD, FT-IR, and TG–DTA. Catalytic properties were studied as one of properties of various rare earth phosphates. Specific surface areas of samples were measured by the BET method. Acid strengths and amounts of acidic sites were measured using several indicators by n-butylamine titration. Acidic properties were also confirmed by adsorption of ammonia. Various rare earth phosphates were characterized by catalytic activities on dehydration reaction of 2-propanol, cracking/dehydrogenation
reaction of cumene, and isomerization reaction of butene. The characterization of catalysts was discussed with regard to type of rare earth elements, type of phosphates, and type of phosphorus resources.

Formation and catalytic characterization of various rare earth phosphates

A novel synthetic dopamine receptor bearing bidentate binding sites were prepared by covalent imprinting using a disulfide linkage which is cleaved and oxidized to a non-covalent sulfoxide recognition group. The used templates have dopamine-like structures connected to an allyl moiety via a disulfide and to a 4-vinylphenyl group via a cyclic boronic diester. After the polymerization, the ester bonds were hydrolyzed and the disulfide bond was reduced to remove the template moiety from the polymer matrix, followed by the oxidation to transform the thiol residues into sulfonic acid (post imprinted process). The imprinted polymer adsorbed dopamine selectively in aqueous solution with the two-point interaction, i.e. the formation of cyclic boronic diester and electrostatic interaction with the sulfonic acid residue.

Dopamine selective molecularly imprinted polymers via post-imprinting modification

Syntheses of various rare earth phosphates from some rare earth compounds

The liquid-phase deposition (LPD) reaction and the deposition mechanisms for the preparation of hazy TiO2, transparent TiO2, and NH4TiOF3 films were investigated by quantitative 19F NMR analysis. Contrary to the conventional understanding, the 19F NMR spectra indicated that BF3(OH)− formed within a short reaction time, and the concentration of BF3(OH)− was always much higher than that of BF4– during the LPD reaction. Quantitative analysis also indicated that several types of titanium complexes coordinated by fluoride ions dissolved in the LPD reaction solutions, but they were not detected by 19F NMR measurement because of rapid ligand substitution. A highly dense and transparent anatase TiO2 thin film was obtained at pH 3.5, and the growth of the particles comprising the films was accelerated by increasing the pH. Conversely, nucleation and crystal growth in the thin films were suppressed at lower pH. Furthermore, in the induction period of the LPD reaction, a shift of chemical equilibrium, which decrease...

Hideshi Maki

Papers

Formation and catalytic characterization of various rare earth phosphates

Dopamine selective molecularly imprinted polymers via post-imprinting modification

Syntheses of various rare earth phosphates from some rare earth compounds

Ionic Equilibria for Synthesis of TiO2 Thin Films by the Liquid-Phase Deposition

Mechanochemical effects of some rare-earth ultraphosphates and reforming of their surface for catalytic properties