TURNING-OVER OF THE ELECTRIC DIPOLE IN A POLYMER*

The transition from the biexciton to the exciton can turn over the direction of the electric dipole of a polymericmolecule. This turning-over action combined with the photoinduced polarization reversion can be used as a switch. Theswitching speed is governed by the relaxation time of the turning-over process, which can be determined by a dynamicalsimulation.     

Mechanism Study for Thermal/Electric Field Poling of Fused Silica

On the basis of the experimental reports, the mechanism of the second-order susceptibility ⁽²⁾ for the thermal/electric field poling of fused silica is analyzed, and expressions for ⁽²⁾ are detailedly derived and numerically calculated for the first time. By comparison the theoretical value of ⁽²⁾ with the experiment results, we propose that the effective ⁽²⁾ is created via both the interaction of the intense electric field with the third-order susceptibility ⁽³⁾ and the dipole orientation. The theoretical results show that, in the differently applied voltage, the dipole orientation and ⁽³⁾ play different role in the formation of ⁽²⁾. This theory successfully explains some experiment results.     

Nuclear electric dipole moments at ion storage rings

Upper limits on the electric dipole moments (EDM) of elementary particles and atoms are presented, and their physical implications are discussed. The implications following from the neutron and atomic experiments are of comparable interest. The nuclear EDMs can be studied at ion storage rings, with the expected sensitivity much better than . This would represent a serious progress in studies of the CP-violation problem. This revised version was published online in August 2006 with corrections to the Cover Date.     

垂直电偶极子在球外侧电磁场的闭合解及验证

给出了理想导体球外侧垂直电偶极子激励电场的闭合解，解决了直接场的级数表达式的不连续性问题.同球外电磁场直接级数求和表达式的计算结果进行了比较.在相同的电磁模型下，利用闭合解对一种近似方法进行了验证：当垂直电偶极子以及场点在球体表面附近并且频率较低时，这两种方法的计算结果非常一致；当垂直电偶极子以及场点不在球体表面附近并且频率较高时，闭合解的计算结果逐渐出现了近似方法未出现的干涉现象.     

Line intensities in the 1.5-μm spectral region of acetylene

Line intensities are measured for 546 transitions belonging to 13 bands of the main isotopologue ¹²C₂H₂ of the acetylene molecule, in the 1.5-μm spectral domain. A multispectrum fitting procedure is used to retrieve line parameters from Fourier transform spectra. Prior to this work, line intensities were known for only 4 bands in this spectral region, from the work of El Hachtouki and Vander Auwera [Absolute line intensities in acetylene: the 1.5 μm region. J Mol Spectrosc 2002;216:355-62]. An excellent agreement is found with the results of these authors, showing that the accuracy of both results is likely better than 1% for the strong bands. However, the spectrum becomes very crowded when one wants to study weaker bands, so that the average accuracy of the intensities reported in the present work is 5%. From these data, vibrational transition dipole moments squared and Herman-Wallis coefficients have been determined for all the bands.     

Structure–reactivity relationships of alkyl α‐hydroxymethacrylate derivatives

A series of alkyl α‐hydroxymethacrylate derivatives with various secondary functionalities (ether, ester, carbonate, and carbamate) and terminal groups (alkyl, cyano, oxetane, cyclic carbonate, phenyl and morpholine) were synthesized to investigate the effect of intermolecular interactions, H‐bonding, π–π interactions, and dipole moment on monomer reactivity. All of the monomers except one ester and one ether derivative are novel. The polymerization rates, determined by using photo‐DSC, showed the average trend (aromatic carbamate > hydroxyl > ester > carbonate ～ aliphatic carbamate ～ ether), with several exceptions due to the differences in terminal groups. There is a correlation between the chemical shift differences of the double bond carbons, the calculated dipole moments, and the reactivities only for nonhydrogen bonded monomers. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

Synthesis and nonlinear optical properties of novel Y‐type polyester containing tricyanovinylthiazolylazoresorcinoxy group with enhanced thermal stability of dipole alignment

Novel Y‐type polyester 4 containing 5‐methyl‐4‐{5‐(1,2,2‐tricyanovinyl)‐2‐thiazolylazo}resorcinoxy groups as nonlinear optical (NLO) chromophores, which are parts of the polymer backbone, was prepared, and its NLO properties were investigated. Polyester 4 is soluble in common organic solvents such as N,N‐dimethylformamide and dimethylsulfoxide. Polymer 4 shows a thermal stability up to 250 °C from thermogravimetric analysis with glass‐transition temperature obtained from differential scanning calorimetry of approximately 94 °C. The second harmonic generation (SHG) coefficient (d₃₃) of poled polymer film at 1560‐nm fundamental wavelength is 8.12 × 10^?9 esu. The dipole alignment exhibits a thermal stability even at 6 °C higher than glass‐transition temperature (T_g), and no significant SHG decay is observed below 100 °C due to the partial main‐chain character of polymer structure, which is acceptable for NLO device applications. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

圆形面偶极层与圆电流的电磁场

通过解电场的轴对称边值问题求出了圆形面偶极层的电势分布，使用其结果和类比方法找到了圆电流的磁场分布。