H2 and O2 Activation—A Remarkable Insight into Hydrogenase

This article summarizes the development of a range of organometallic, biomimetic analogues of [NiFe]hydrogenases and their employment in a new generation of H₂‐O₂ fuel cells. It begins with a summary of O₂‐sensitive and O₂‐tolerant enzyme chemistry before detailing the properties and functionality of our biomimetic complexes, including: the first ever fully functional model, selective H₂ and O₂ activation, and the first catalyst using only common metals. These systems are centered on Ni–Fe, Ni–Ru, Ir–Ir, and Rh–Rh cores and use a range of ligands that all follow a set of design principles described herein.     

Dielectric Multilayer Including Azobenzene Polymer Liquid Crystal with Non-quarter-wave Stack

Dielectric multilayer including azobenzene polymer liquid crystal acts as a one-dimensional photonic crystal and has optical-switchable reflection bands. The reflection intensity can be controlled by irradiation of ultraviolet (UV) or visible light, in which the optical switch is based on cis-trans photoisomerization. An increase in the number of layers prevents photoresponse in the multilayer including azobenzen layers because UV or visible light for control cis-trans isomerization hardly reach the bottom of the multilayer due to exponential decay of light intensity. In this study, the multilayer consisting of thin azobenzene layers is investigated. According to numerical calculations, the non-quarter-wave structured multilayer has multiwavelength reflection band. Angular dependence of reflection color from multiwavelength stopband is also studied using the XYZ color space. The non-quarter-wave multilayer suppresses reflection color change compared with conventional quarter-wave multilayer.     

A Theoretical and Experimental Study of the Effects of Silyl Substituents in Enantioselective Reactions Catalyzed by Diphenylprolinol Silyl Ether

The effect of silyl substituents in diphenylprolinol silyl ether catalysts was investigated. Mechanistically, reactions catalyzed by diphenylprolinol silyl ether can be categorized into three types: two that involve an iminium ion intermediate, such as for the Michael‐type reaction (type A) and the cycloaddition reaction (type B), and one that proceeds via an enamine intermediate (type C). In the Michael‐type reaction via iminium ions (type A), excellent enantioselectivity is realized when the catalyst with a bulky silyl moiety is employed, in which efficient shielding of a diastereotopic face of the iminium ion is directed by the bulky silyl moiety. In the cycloaddition reaction of iminium ions (type B) and reactions via enamines (type C), excellent enantioselectivity is obtained even when the silyl group is less bulky and, in this case, too much bulk reduces the reaction rate. In other cases, the yield increases when diphenylprolinol silyl ethers with bulky substituents are employed, presumably by suppressing side reactions between the nucleophilic catalyst and the reagent. The conformational behaviors of the iminium and enamine species have been determined by theoretical calculations. These data explain the effect of the bulkiness of the silyl substituent on the enantioselectivity and reactivity of the catalysts.     

High-Pressure Solubility of l-Methionine in Water

The solubility (m _S) of l-methionine in water was measured at 298.2 K and pressures up to 200 MPa. The data were fitted to the equation ln(m _S/mol·kg^?1) = ?4.62 × 10^?6 (p/MPa)² + 2.65 × 10^?3 (p/MPa) ? 0.970 with a standard deviation of σ(ln m _S) = 0.002. The pressure coefficient of the logarithm of solubility (?ln m _S/?p) _T was thermodynamically estimated to be (2.62 ± 0.34) × 10^?3 MPa^?1 at 0.10 MPa using several parameters such as partial molar volume and activity coefficient of l-methionine in water and molar volume of solid l-methionine. The resulting value agrees well with the second term on the right-hand side of the fitted equation above, indicating the reliability of the high-pressure solubility measurements. The value of (?ln m _S/?p) _T also was compared with those of other amino acids.     

Recognition of gram-negative and gram-positive bacteria with a functionalized conducting polymer film

In this work, we successfully developed bacterial templates on the surface of an overoxidized polypyrrole film using both gram-negative and gram-positive bacteria in which bacterial surface chemical structures are precisely transferred at a molecular level. The sensor film identified target bacteria within minutes through a unique combination with dielectrophoresis. The bacterial cavities had high selectivity for distinguishing specific target bacteria in bacterial mixtures containing gram-negative (Escherichia coli and Pseudomonas aeruginosa) and gram-positive (Bacillus subtilis and Staphylococcus aureus) bacteria. This rapid and specific recognition system will enable not only bacterial sensing but also analysis of various biological species.     

Intracellular in vitro probe acylcarnitine assay for identifying deficiencies of carnitine transporter and carnitine palmitoyltransferase-1

Mitochondrial fatty acid oxidation (FAO) disorders are caused by defects in one of the FAO enzymes that regulates cellular uptake of fatty acids and free carnitine. An in vitro probe acylcarnitine (IVP) assay using cultured cells and tandem mass spectrometry is a tool to diagnose enzyme defects linked to most FAO disorders. Extracellular acylcarnitine (AC) profiling detects carnitine palmitoyltransferase-2, carnitine acylcarnitine translocase, and other FAO deficiencies. However, the diagnosis of primary carnitine deficiency (PCD) or carnitine palmitoyltransferase-1 (CPT1) deficiency using the conventional IVP assay has been hampered by the presence of a large amount of free carnitine (C0), a key molecule deregulated by these deficiencies. In the present study, we developed a novel IVP assay for the diagnosis of PCD and CPT1 deficiency by analyzing intracellular ACs. When exogenous C0 was reduced, intracellular C0 and total AC in these deficiencies showed specific profiles clearly distinguishable from other FAO disorders and control cells. Also, the ratio of intracellular to extracellular C0 levels showed a significant difference in cells with these deficiencies compared with control. Hence, intracellular AC profiling using the IVP assay under reduced C0 conditions is a useful method for diagnosing PCD or CPT1 deficiency.     

Tailoring of the desired selectivity and the turn-on detection range in a self-assembly-based fluorescence sensory system

This study demonstrates how to control the selectivity and the turn-on detection range toward the tailoring of an assembly-based fluorescence (FL) sensory system. Assembly-based FL chemosensors composed of oligophenylenevinylene with a varied number of guanidinium receptors (G2, G4 and G6) were newly developed, and their FL response to nucleotides (AMP, ADP and ATP) was investigated. Indeed, G6 exhibited FL emission via self-assembly with ATP. More importantly, the FL response of G6 showed markedly improved selectivity for ATP over ADP and a broadly extended detection range of ATP concentration under adjusted salt conditions. The salt effect on the FL response revealed the competitive binding interactions affecting the subsequent self-assembly process. These studies have unveiled the pivotal binding mechanisms operating in the self-assembly process, which tailor the performance level of the assembly-based sensory system. We believe that this study offers a new design principle of an assembly-based FL chemosensor with high selectivity and the appropriate detection range, being different from the conventional key-and-lock system.     

Williamson Ether Synthesis with Phenols at a Tertiary Stereogenic Carbon: Formal Enantioselective Phenoxylation of β‐Keto Esters

The enantioselective formation of α‐aryloxy‐β‐keto esters is described for the first time. Lewis acid catalyzed enantioselective chlorination of β‐keto esters and subsequent S_N2 reactions with phenols yielded α‐aryloxy‐β‐keto esters with up to 96 % ee. Favorskii rearrangement of α‐chloro‐β‐keto esters was also found to give 1,2‐diesters with slightly reduced enantiopurity.     

Tetraalkylammonium Salts as Hydrogen‐Bonding Catalysts

Although the hydrogen‐bonding ability of the α hydrogen atoms on tetraalkylammonium salts is often discussed with respect to phase‐transfer catalysts, catalysis that utilizes the hydrogen‐bond‐donor properties of tetraalkylammonium salts remains unknown. Herein, we demonstrate hydrogen‐bonding catalysis with newly designed tetraalkylammonium salt catalysts in Mannich‐type reactions. The structure and the hydrogen‐bonding ability of the new ammonium salts were investigated by X‐ray diffraction analysis and NMR titration studies.