Hyperspherical slow variable discretization method for weakly bound triatomic molecules

We develop a method for calculating the bound state energies and the wave functions of weakly bound triatomic molecular systems. The method is based on the use of hyperspherical coordinates, combined with the slow variable discretization approach. The finite-element methods-discrete variable representation scheme provides an efficient means to solve the coupled-channel hyper-radial equations. Our method is applied to searching for bound states of the (20)Ne(2)H and (4)He(20)NeH triatomic molecules, using the best empirical pairwise interaction potentials. We consider not only zero total nuclear orbital momentum, J = 0, states but also J > 0 states. The (20)Ne(2)H system has been found to possess one bound state each for the J(Π)=0(+),1(-), and 2(+) symmetries, while there exist only one bound state for the (4)He(20)NeH system in the 0(+) symmetry. We shall calculate the bound state energies and analyze the molecular structures of these species in detail.     

Use of dimethyl carbonate as a solvent greatly enhances the biaryl coupling of aryl iodides and organoboron reagents without adding any transition metal catalysts

The coupling reaction of aryl iodides with arylboronic acids to give biaryl compounds can be efficiently performed without adding a transition metal catalyst. The key to success is the use of dimethyl carbonate as a solvent. This finding provides a new strategy for constructing a biaryl linkage.     

Maximal minors of a matrix with linear form entries

Let P be a matrix whose entries are homogeneous polynomials in n variables of degree one over an algebraically closed field. We show that the maximal minors, say m-minors, of P generate the linear space of homogeneous polynomials of degree m if P has the maximal rank m at every point of the affine n-space except the origin.     

The "off-on" fluorescence detection of alkaline earth metal ions by using 1-naphthylacetanilide derivatives: new cation sensors based on oligo-ethylene oxides connecting 1-naphthylacetanilide at its terminals.

New fluorescent ionophores containing the 1-naphthylacetanilide moiety based on oligo-ethylene oxide (1(4) and 1(5)) have been synthesized, and their photochemical behaviors have been studied. In the absence of a metal ion, the 1-naphthylacetanilide moiety showed a weak fluorescence emission (fluorescence "off state"). However, complexation with Ca(2+) induced a large enhancement effect on the fluorescence intensity of 1(4) and 1(5) from the naphthalene ring (fluorescence "on" state). This behavior can be explained in terms of a similar twisted intramolecular charge-transfer relaxation mechanism. Such "off-on" fluorescence responses of 1(4) and 1(5) provide the digital detection of alkaline earth metal ions.     

Cyclization reactions of homopropargyl azide derivatives catalyzed by PtCl4 in ethanol solution: synthesis of functionalized pyrrole derivatives

[Structure: see text] PtCl4-catalyzed cyclization reactions of homopropargyl azide derivatives to pyrrole rings were investigated. Using ethanol as solvent with 2,6-di-tert-butyl-4-methylpyridine as the base was found to be the best set of conditions for effecting this ring-closing reaction. These reaction conditions can be applied to the preparation of functionalized pyrrole derivatives, with no effect on the functional groups.     

Exciton recurrence motion in aggregate systems in the presence of quantized optical fields

The exciton dynamics of model aggregate systems, dimer, trimer, and pentamer, composed of two-state monomers is computationally investigated in the presence of three types of quantized optical fields, i.e., coherent, amplitude-squeezed, and phase-squeezed fields, in comparison with the case of classical laser fields. The constituent monomers are assumed to interact with each other by the dipole-dipole interaction, and the two-exciton model, which takes into account both the one- and two-exciton generations, is employed. As shown in previous studies, near-degenerate exciton states in the presence of a (near) resonant classical laser field create quantum superposition states and thus cause the spatial exciton recurrence motion after cutting the applied field. In contrast, continuously applied quantized optical fields turn out to induce similar exciton recurrence motions in the quiescent region between the collapse and revival behaviors of Rabi oscillation. The spatial features of exciton recurrence motions are shown to depend on the architecture of aggregates. It is also found that the coherent and amplitude-squeezed fields tend to induce longer-term exciton recurrence behavior than the phase-squeezed field. These features have a possibility for opening up a novel creation and control scheme of exciton recurrence motions in aggregate systems under the quantized optical fields.     

Thermodynamics of Hydrophobic Interactions: Entropic Recognition of a Hydrophobic Moiety by Poly(Ethylene Oxide)–Zinc Porphyrin Conjugates

The recognition of 4‐alkylpyridines by water‐soluble poly(ethylene oxide)–zinc porphyrin conjugates was studied with a focus on the thermodynamic parameters of binding. Microcalorimetric studies indicated that binding of the alkyl group of the guest in water is driven by the entropic term (δΔH⁰=ΔH⁰(4‐pentylpyridine)? ΔH⁰(4‐methylpyridine)=+1.7 kJ mol^?1, δTΔS⁰=TΔS⁰(4‐pentylpyridine)? TΔS⁰(4‐methylpyridine)=+11.8 kJ mol^?1 at 298 K), thus showing the significance of water reorganization during host–guest interaction. The enthalpy–entropy compensation temperature of binding of 4‐alkylpyridines was as low as 38 K; only below this temperature could the enthalpic term be a driving force. The binding affinity was modulated by the addition of cations and by varying the degree of polymerization of poly(ethylene oxide), which suggests that guest binding is coupled with polymer conformation.     

Preparation and characterization of a polyclonal antibody from rabbit for detection of trinitrotoluene by a surface plasmon resonance biosensor

A polyclonal antibody against trinitrophenyl (TNP) derivatives was raised in rabbit, and the antibody was applied to detection of trinitrotoluene (TNT) using a surface plasmon resonance (SPR) biosensor. TNP-keyhole limpet hemocyanine (TNP-KLH) conjugate was injected into a rabbit, and a polyclonal anti-TNP antibody was realized after purification of the sera using protein G. Aspects of the anti-TNP antibody against various nitroaromatic compounds, such as cross-reactivities and affinities, were characterized. The temperature dependence of the affinity between the anti-TNP antibody and TNT was also evaluated. The quantification of TNT was based on the principle of indirect competitive immunoassay, in which the immunoreaction between the TNP-β-alanine-ovalbumin (TNP-β-ala-OVA) and anti-TNP antibody was inhibited in the presence of free TNT in solution. TNP-β-ala-OVA was immobilized to the dextran matrix on the Au surface by amine coupling. The addition of a mixture of free TNT to the anti-TNP antibody was found to decrease the incidence angle shift due to the inhibitory effect of TNT. The immunoassay exhibited excellent sensitivity for the detection of TNT in the concentration range of 3 × 10⁻¹¹ to 3 × 10⁻⁷ g/ml. To increase the sensitivity of the sensor, anti-rabbit IgG antibody was used. After flowing the mixture of free TNT and anti-TNP antibody, anti-rabbit IgG antibody was injected, and the incidence angle shift was measured. Amplification of the signal was observed and the detection limit was improved to 1 × 10⁻¹¹ g/ml.