A recyclable, self-supported organocatalyst based on a poly(N-heterocyclic carbene)

We report the synthesis and catalytic activity of a polymeric imidazolium salt. In contrast to the well-known resin-supported N-heterocyclic carbenes (NHCs), the material described herein affords a polymer with NHCs orthogonally positioned along a main chain upon generation in situ. The unique structural characteristics of the corresponding poly(NHC)s enabled the materials to display catalytic activities that were similar or superior to those displayed by monomeric analogues. Moreover, the new catalyst was successfully recovered and reused with minimal loss of performance over several cycles.     

Numerical simulation of cyclic voltammetry for reversible systems with complex stoichiometry

Reversible waves of voltammetry with complex non-unity stoichiometry are studied here based on theory. Numerical simulations were performed for various stoichiometric systems in which coefficients m and q were independently varied from 1 to 4 in a general reaction scheme, mO + ne⁻ ai qR. The calculation results indicate that the peak current function at complex stoichiometry differs from that at simple unity stoichiometry. The relation between the half-wave potential and the formal potential has been partially corrected from that previously reported in the literature. Parameters in the relation between the peak potential and the half-wave potential are unique for each stoichiometric system. The parameter in the relation between the peak potential and the half-peak potential is also presented here.     

1,5]-H shift of aldehyde hydrogen in dienal compounds to produce ketenes

In 3-ethoxycarbonyl-2,4-dienal compounds, a thermal [1,5]-H shift of aldehyde hydrogen easily proceeded to produce the corresponding vinyl ketenes due to the remarkable substituent effect caused by the C3 ester group. The produced ketenes were captured by an alcohol and olefins to afford the corresponding esters and four-membered ring compounds, respectively.     

On distorted probabilities and m-separable fuzzy measures

Fuzzy measures are used in conjunction with fuzzy integrals for aggregation. Their role in the aggregation is to permit the user to express the importance of the information sources (either criteria or experts). Due to the fact that fuzzy measures are set functions, the definition of such measures requires the definition of 2ⁿ parameters, where n is the number of information sources. To make the definition easier, several families of fuzzy measures have been defined in the literature.In this paper m-separable fuzzy measures are introduced. We present some results on this type of measures and we relate them to some of the previous existing ones. We study generating functions for m-separable fuzzy measures and some properties related to these generating functions.     

Synthesis and study of redox-active acyclic triazenes: toward electrochromic applications

Coupling of various 4-substituted phenyl azides with two distinct quinone-containing N-heterocyclic carbenes (NHCs) afforded the respective mono- and ditopic 1,3-disubstituted acyclic triazenes in moderate to excellent yields (38-92%). Depending on their pendant substituents (derived from the azides), the acyclic triazenes exhibited intense absorptions in the visible spectrum (359-428 nm), which were bathochromically shifted by up to Δλ=68 nm upon reduction of the quinone moiety on the component derived from the NHC. Cyclic voltammetry confirmed that the aforementioned redox processes were reversible, and a related set of UV-vis spectroelectrochemical experiments revealed that bulk electrolysis may also be used to switch reversibly the colors exhibited by these triazenes.     

Highly efficient enzymatic synthesis of 3'-deoxyapionucleic acid (apioNA) having the four natural nucleobases

The synthesis of the 3'-deoxyapionucleoside 3'-triphosphates (apioNTPs) having the four natural nucleobases and their enzymatic incorporation into a DNA-DNA primer-template have been tried. Therminator DNA polymerase was shown to incorporate these apioNTPs effectively giving 43mer DNA-apioNA chimera.     

Design and synthesis of new chiral phosphorus-olefin bidentate ligands and their use in the rhodium-catalyzed asymmetric addition of organoboroxines to N-sulfonyl imines

Novel chiral phosphorus-olefin bidentate ligands have been synthesized in a few steps from a readily available enantiopure compound. These ligands have been applied to a rhodium-catalyzed asymmetric addition of organoboroxines to N-sulfonyl aldimines, achieving high yield and enantioselectivity.     

New method for comprehensive detection of chemical warfare agents using an electron-cyclotron-resonance ion-source mass spectrometer

We developed a detection technology for vapor forms of chemical warfare agents (CWAs) with an element analysis system using an electron cyclotron resonance ion source. After the vapor sample was introduced directly into the ion source, the molecular material was decomposed into elements using electron cyclotron resonance plasma and ionized. The following CWAs and stimulants were examined: diisopropyl fluorophosphonate (DFP), 2-chloroethylethylsulfide (2CEES), cyanogen chloride (CNCl), and hydrogen cyanide (HCN). The type of chemical warfare agents, specifically, whether it was a nerve agent, blister agent, blood agent, or choking agent, could be determined by measuring the quantities of the monatomic ions or CN(+) using mass spectrometry. It was possible to detect gaseous CWAs that could not be detected by a conventional mass spectrometer. The distribution of electron temperature in the plasma could be closely controlled by adjusting the input power of the microwaves used to generate the electron cyclotron resonance plasma, and the target compounds could be detected as molecular ions or fragment ions, enabling identification of the target agents.     

On the global wellposedness for the nonlinear Schrödinger equations with L p -large initial data

We consider the Cauchy problem for the nonlinear Schrödinger equations $ \begin{array}{l} iu_t + \triangle u \pm |u|^{p-1}u =0, \qquad x \in \mathbb{R}^d, \quad t \in \mathbb{R} \\ u(x,0)= u_0(x), \qquad x \in \mathbb{R}^d \end{array} $ for 1 < p < 1 + 4/d and prove that there is a ${\rho (p ,d) \in (1,2)}We consider the Cauchy problem for the nonlinear Schr?dinger equations

l iut + \triangle u ±|u|p-1u = 0,        x ? \mathbbRd,     t ? \mathbbR u(x,0) = u0(x),        x ? \mathbbRd \begin{array}{l} iu_t + \triangle u \pm |u|^{p-1}u =0, \qquad x \in \mathbb{R}^d, \quad t \in \mathbb{R} \\ u(x,0)= u_0(x), \qquad x \in \mathbb{R}^d \end{array}      140. The Cauchy problem for hyperbolic systems with Hölder continuous coefficients with respect to time      Yasuo Yuzawa 《Journal of Differential Equations》2005,219(2):363-374 We discuss the local existance and uniqueness of solutions of certain nonstrictly hyperbolic systems, with Hölder continuous coefficients with respect to time variable. We reduce the nonstrictly hyperbolic systems to the parabolic ones, then we shall prove them by use of Tanabe-Sobolevski’s method.      [首页] « 上一页 [9] [10] [11] [12] [13] 14 [15] [16] [17] [18] [19] 下一页 » 末  页»

The Cauchy problem for hyperbolic systems with Hölder continuous coefficients with respect to time

We discuss the local existance and uniqueness of solutions of certain nonstrictly hyperbolic systems, with Hölder continuous coefficients with respect to time variable. We reduce the nonstrictly hyperbolic systems to the parabolic ones, then we shall prove them by use of Tanabe-Sobolevski’s method.