Solvent and temperature-dependent conductive behavior of poly(3-hexylthiophene)

Impedance characterization at different temperatures has been used to investigate the conductive behavior of Poly(3-hexylthiophene) (P3HT), prepared in different solvents, as the semiconductor layer in organic multilayer capacitor. It has been found that the P3HT films using chloroform and toluene solvents exhibit an enhancement in conductivity by heating following an Arrhenius law with an activation energy transition from 0.004 to 0.026 eV and from 0.002 to 0.015 eV at ~313 K, respectively, which originates from band tail hopping that occurs around the Fermi edge. The boiling point of the used solvents can affect P3HT crystallization process, which causes the difference in conduction and activation energy.     

量子Generalized Reed-Solomon码

构造出了一族量子纠错码，这族码具有参数［［n，n-2k，k+1］］_q，是q维量子系统上的码，q是任意素数的幂.这族码的最小距离达到了理论上限，因此，以码距来说，它是最优的.证明了当2≤n≤q或者q²-q+2≤n≤q²时，码都是存在的.     

Direct visualization of layer-by-layer self-assembled multilayers of organometallic polymers

Direct visualization of organometallic-organic and novel all-organometallic multilayer superlattices prepared by layer-by-layer assembly of cationic/anionic polyferrocenylsilane and anionic polystyrene sulfonate polyelectrolytes using a gold coating/transmission electron microscopy (TEM) technique is reported.     

分布式系统的层次式命名方案设计

针对大规模分布式系统中对象迁移、网络和系统动态重构的要求,本文提出了一种层次式的命名和编址方案,它将对位置透明的标识（ＯＩＤ）和表示位置的地址（ＯＡＤ）二者结合起来标识对象．     

Small peptides catalyze highly enantioselective direct aldol reactions of aldehydes with hydroxyacetone: unprecedented regiocontrol in aqueous media

[reaction: see text] L-Proline-based small peptides have been developed as efficient catalysts for the asymmetric direct aldol reactions of hydroxyacetone with aldehydes. Chiral 1,4-diols 7, which are disfavored products in similar aldol reactions catalyzed by either aldolases or L-proline, were obtained in high yields and enantioselectivities of up to 96% ee with peptides 3 and 4 in aqueous media.     

Enzymatic ring-opening copolymerization of trimethylene carbonate and ethylene ethyl phosphate

A growing interest in biodegradable polymers and their biomedical and pharmaceutical applications has developed since the past decade. Ring-opening polymerization has been regarded as an efficient route for the synthesis of the biodegradable polymers, such as polyester, polycar- bonates and polyphosphates[1—6]. However, chemical methods for the ring-opening polymerization of biodegradable polymers need extremely pure monomers and anhydrous conditions as well as metallic catalysts, which must …     

Rules on pair electron correlation in MOH (M=H,Li, Na)

In this article, the transferable property of pair correlation energies of OH components is discussed for a series of OH containing compounds MOH (M=H, Li, Na). In this series of compounds, from OH free radicals through HOH, LiOH, NaOH to OH^?, both the intra‐ and interpair correlation energies and intra‐ and intershell correlation energies of the inner orbital electrons change little. The 1s$_{\mathrm{O}}^{2}$ is very much alike in all the above OH containing systems and such a pair correlation is transferable. But the interpair correlation and intrashell correlation energies of the valence electrons are large and change a lot in all systems. In MOH molecules, the OH correlation energy contribution increases with the increase of the ionic bond strength of the compound and this contribution is always between the correlation energy values of OH free radicals and OH^? atomic groups. For strong ionic compounds, we present a very simple method to estimate the correlation energy by adding the correlation energies of its component ions within the chemical accuracy (2 kcal/mol). © 2001 John Wiley & Sons, Inc. Int J Quant Chem 83: 311–317, 2001     

非线性光学格子中的光束演化研究

研究光学格子中(即在光传输的横截面上存在周期格子势的调制)光束的演化，利用变分原理，求出了光束宽度、振幅、频率啁啾参量随传播距离的演化形式.发现光束宽度与调制周期的比值必须小于一定的值才能形成孤子的传输；同时，还得到了光束在不同的条件下存在着不同的传输过程.光学格子中周期格子的作用有类似非线性的良好的特性，周期格子的引入提供了可以更好地控制格子孤子的形成和传输的参考条件.     

Influence of nonlinear dispersion on modulation instability of coherent and partially coherent ultrashort pulses in metamaterials

The combination of dispersive magnetic permeability with nonlinear polarization leads to a series of nonlinear dispersion terms in the propagation equations for ultrashort pulses in metamaterials. Here we present an investigation of modulation instability (MI) of both coherent and partially coherent ultrashort pulses in metamaterials to identify the role of nonlinear dispersion in pulse propagation. The Wigner–Moyal equation for partially coherent ultrashort pulses and the nonlinear dispersion relation for MI in metamaterials are derived. Combining the standard MI theory with the unique properties of the metamaterial, the influence of the controllable first-order nonlinear dispersion, namely self-steepening, and the second-order nonlinear dispersion on both coherent and partially coherent MI, in both negative-index and positive-index regions of the metamaterial for all physically possible cases is analyzed in detail. For the first time to our knowledge, we demonstrate that the role of the second-order nonlinear dispersion in MI is equivalent to that of group-velocity dispersion (GVD) to some extent, and thus due to the role of the second-order nonlinear dispersion, MI may appear in the otherwise impossible cases, such as in the normal GVD regime. PACS 42.25.Kb; 42.65.Sf; 78.20.Ci     

Synthesis of 2,2,6,6-tetrafluoro-4-phenylmethylmorpholin-3-ones: A simple approach from fluorinated triethylene glycol

2,2,6,6-Tetrafluoro-4-phenylmethylmorpholin-3-ones are obtained from a new single step, preparative route by reacting triethylene glycol di(trifluoromethanesulfonate), which contains poly -CF₂O- groups, with benzylamine. Reaction of trifluoromethylsulfonate and trifluoromethoxy derivatives with benzylamine gave either the nucleophilically-substituted product or the product resulting from the basic hydrolysis of the difluoromethoxy group. Replacement of a fluoroether chain by a fluoroalkane gave rise to fluorinated phenylmethylpiperidine and phenylmethylazepine via the combination of trifluoromethanesulfonic fluoroalkyldiyl esters and benzylamine.