Topological particle field theory,general coordinate invariance and generalized Chern-Simons actions

We show that recently proposed generalized Chern-Simons action can be identified with the field theory action of a topological point particle. We find the crucial correspondence which makes it possible to derive the field theory actions from a special version of the generalized Chern-Simons actions. We provide arguments that the general coordinate invariance in the target space and the flat connection condition as a topological field theory can be accommodated in a very natural way. We propose series of new gauge invariant observables.     

Effects of dissolved gas species on ultrasonic degradation of (4-chloro-2-methylphenoxy) acetic acid (MCPA) in aqueous solution

Sonochemical degradation of MCPA ((4-chloro-2-methylphenoxy) acetic acid) in dilute aqueous solutions was studied using ultrasound with a frequency of 500 kHz. The effect of gas atmosphere on MCPA degradation was investigated in nitrogen (N(2)), air (O(2)/N(2)), oxygen (O(2)), argon (Ar) and Ar/O(2) (60/40% v/v) atmospheres. For sonochemical degradation of MCPA in N(2), air (O(2)/N(2)), O(2) and Ar atmospheres, the rate enhancement of MCPA decomposition by sonolysis was found to be more effective in an O(2)-enriched atmosphere compared to Ar atmosphere. It was considered that a higher amount of oxidants was formed in a higher O(2) partial pressure, which accelerated MCPA decomposition in a radical reaction system. On the other hand, both dechlorination and total organic carbon (TOC) removal rates were higher in Ar atmosphere, compared to those in O(2)/N(2) atmosphere. It was found that, MCPA was most effectively decomposed by sonication in Ar/O(2) (60/40% v/v) atmosphere, with higher rates of decomposition, dechlorination and TOC removal.     

Determination of bisphenol A with effective pretreatment medium using automated column-switching HPLC with fluorescence detection

A practical way for reducing contaminants, such as humic acids, and solving column-clogging problem in environmental water analysis with liquid chromatography is proposed. Detection interference by contamination is one of the most important issues of the environmental analyses. Moreover, due to the recent smaller diameter and fine particle size of an analytical column for HPLC system, a column-clogging problem is another practical difficulty as well. We found it possible to solve these problems by employing column-switching HPLC, which consists of a pretreatment column containing surface-modified polymer particles and flow changeover valves for cleaning the remaining matrices in the pretreatment column prior to analysis. This method was successfully applied to actual HPLC-fluorescence detection of bisphenol A. Limit of detection (LOD) in real sample was <0.7 ng/L. Repeatability was around 1.4% and recovery was around 97% or more. A particular pressure increase was not observed in 150 repeated analyses of real river water samples.     

Dimeric copper(II) trimethylsilyl­acetate adducts with pyridine, 2‐­methylpyridine, 3‐methylpyridine and quinoline,and a polymeric copper(II) trimethylsilylacetate

In the crystals of bis(pyridine‐N)tetrakis(μ‐trimethylsilylacetato‐O:O′)dicopper(II), [Cu₂(C₅H₁₁O₂Si)₄(C₅H₅N)₂], (I), the dinuclear Cu^II complexes have cage structures with Cu?Cu distances of 2.632 (1) and 2.635 (1) Å. In the crystals of bis(2‐­methylpyridine‐N)tetrakis(μ‐trimethylsilylacetato‐O:O′)dicopper(II), [Cu₂(C₅H₁₁O₂Si)₄(C₆H₇N)₂], (II), bis­(3‐methylpyridine‐N)tetrakis(μ‐trimethylsilylacetato‐O:O′)dicopper(II), [Cu₂(C₅H₁₁O₂Si)₄(C₆H₇N)₂], (III), and bis(quinoline‐N)­tetrakis(μ‐­trimethylsilylacetato‐O:O′)dicopper(II), [Cu₂(C₅H₁₁O₂Si)₄(C₉H₇N)₂], (IV), the centrosymmetric dinuclear Cu^II complexes have a cage structure with Cu?Cu distances of 2.664 (1), 2.638 (3) and 2.665 (1) Å, respectively. In the crystals of catena‐poly­[tetrakis(μ‐trimethylsilylacetato‐O:O′)dicopper(II)], [Cu₂(C₅H₁₁O₂Si)₄]_n, (V), the dinuclear Cu^II units of a cage structure are linked by the cyclic Cu—O bonds at the apical positions to form a linear chain by use of a glide translation.     

Dimeric copper(II) 3,3‐dimethyl­butyrate adducts with ethanol, 2‐methylpyridine, 3‐methylpyridine, 4‐methylpyridine and 3,3‐dimethylbutyric acid

In the crystals of the five title compounds, tetrakis‐(μ‐3,3‐dimethylbutyrato‐O:O′)bis(ethanol‐O)dicopper(II)–ethanol (1/2), [Cu₂(C₆H₁₁O₂)₄(C₂H₆O)₂]·2C₂H₆O, (I), tetrakis(μ‐3,3‐dimethylbutyrato‐O:O′)bis(2‐methylpyridine‐N)di­copper(II), [Cu₂(C₆H₁₁O₂)₄(C₆H₇N)₂], (II), tetrakis‐(μ‐3,3‐dimethylbutyrato‐O:O′)bis(3‐methylpyridine‐N)di‐copper(II), [Cu₂(C₆H₁₁O₂)₄(C₆H₇N)₂], (III), tetrakis‐(μ‐3,3‐dimethylbutyrato‐O:O′)bis(4‐methylpyridine‐N)di‐copper(II), [Cu₂(C₆H₁₁O₂)₄(C₆H₇N)₂], (IV), and tetrakis‐(μ‐3,3‐dimethylbutyrato‐O:O′)bis(3,3‐dimethylbutyric acid‐O)dicopper(II), [Cu₂(C₆H₁₁O₂)₄(C₆H₁₂O₂)₂], (V), the di­nuclear Cu^II complexes all have centrosymmetric cage structures and (IV) has two independent molecules. The Cu?Cu separations are: (I) 2.602 (3) Å, (II) 2.666 (3) Å, (III) 2.640 (2) Å, (IV) 2.638 (4) Å and (V) 2.599 (1) Å.     

(1R,2R,3S,4S)‐2‐[(2R,3S)‐2,3‐Di­methyl­oxiran‐2‐yl]‐3,4‐bis(4‐methoxy­benzyl­oxy)­cyclo­hexanol

The relative configuration was determined for the title com­pound, C₂₆H₃₄O₆, which was prepared in a synthetic study on immunosuppressant FR­65­814. There is an intra­mol­ecular hydrogen bond between the hydroxy and epoxy groups.     

Equatorial preference in the C[bond]H activation of cycloalkanes: GaCl3-catalyzed aromatic alkylation reaction

GaCl(3) catalyzes the aromatic alkylation of naphthalene or phenanthrene using cycloalkanes. The C[bond]C formation predominantly takes place at the least hindered positions of the substrates, and equatorial isomers regarding the cycloalkane moiety are generally obtained. The reaction of bicyclo[4.4.0]decane and naphthalene occurs at the 2-position of naphthalene and at the 2- or 3-carbons of the cycloalkane, and the products possess a trans configuration at the junctures and an equatorial configuration at the naphthyl groups. Notably, cis-bicyclo[4.4.0]decane turns out to be much more reactive than the trans isomer, and a turnover number "TON" up to 20 based on GaCl(3) is attained. 1,2-Dimethylcyclohexane reacts similarly, and the cis isomer is more reactive than the trans isomer. Monoalkylcycloalkanes react at the secondary carbons provided that the alkyl group is smaller than tert-butyl. Adamantanes react at the tertiary 1-position. The alkylation reaction is considered to involve the C[bond]H activation of cycloalkanes with GaCl(3) at the tertiary center followed by the migration of carbocations and electrophilic aromatic substitution yielding thermodynamically stable products. The stereochemistry of the reaction reveals that GaCl(3) activates the equatorial tertiary C[bond]H rather than the axial tertiary C[bond]H.     

Synthesis and electrochemical studies of ferrocene-dithiafulvalenes (Fc-DTF) and 1,1′-bis(dithiafulvalenyl)ferrocene (DTF-Fc-DTF). An approach towards new conducting organic materials

Novel π-conjugated donor compounds based on the strong electron-donating ferrocene moiety and dithiafulvalene donors exhibited increased electron donor ability. The ferrocenylketones 4a,b, 5, 8 and 9 were synthesized via described methods, and allowed to react with 2-dimethoxyphosphinyl-1,3-benzodithiole (13) in the presence of n-BuLi at −78°C in dry THF to afford the corresponding ferrocene-dithiafulvalenes 14a,b, 18, 19 and 1,1′-bis(benzo-1,3-dithiol-2-ylidene)ethyl]ferrocene (15). Electrochemical properties of these new donor compounds were studied using cyclic voltammetry (CV) and UV-Vis spectra. CV and absorption spectra of the new compounds were studied in comparison with ferrocene (6) and dibenzo-tetrathiafulvalene DB-TTF 3. Two-electron and three-electron redox behaviors were observed as two waves. The absorption spectra showed a red-shift with a slight increase in the absorption intensities.     

A fourth scale sensitive to the magnetic field; intermolecular frequency symmetry in a specific interaction between protein and low-molecular compound

We found a new method that a specific interaction between prion, i.e., high-molecular compound, and Cp-60, i.e., low-molecular one, could be successfully elucidated with intermolecular frequency symmetry (IFS). To accomplish this, the former sequence is analyzed with a sequence Fourier analysis used average nuclear (N) resonant frequency scale as a fourth one, and the latter structure with a 13C-NMR software. Further, such the symmetry could be observed in a specific interaction between a segment of human immunodeficiency virus (HIV)gag and PA-457 or between 1918 neuraminidase and peramivir. Therefore, the IFS rule seems to be evolutionarily conserved as a necessary condition even in a specific protein-organic compound interaction.     

GaCl3-Catalyzed ortho-ethynylation reaction of N-benzylanilines

Lithiated N-benzylanilines were ethynylated at the ortho-position with silylchloroethyne at 120 °C in the presence of a catalytic amount of GaCl₃. Trimethylsilylated N-methylaniline could also be used for this transformation.