Efficient Amide Based Halogenide Anion Receptors

In this paper, we present the synthesis and anion recognition properties of the amide based phenanthroline derivatives 1, 2 and 3. In all cases 1:1 receptor : anion complexes were observed. The receptors were found to be selective for fluoride and chloride respectively over other putative anionic guest species.     

具有负指数系数的微分算子的谱

本文研究了形如∑_n~k=o~((α_k)(e~((α_k)x))D~k(a_k≤0)及∑_k~n=o((-1)~k)α_(2k)D~ke~(α_(2k)x)D~k+i/2∑_k~n=o(α_(2k+1))(D~ke~((α_(2k+1))x)D~(k+1)+D~(k+1)e~((α_(2k+1)x)D~k)(α_k≤0)的算式的谱问题,分别得到了它们的本质谱或本质谱所在的范围.     

Synthesis and characterization of novel aromatic poly(imide–benzoxazole) copolymers

New poly(imide–benzoxazole) copolymers were prepared directly from a dianhydride, a diacid chloride, and a bis(o‐diaminophenol) monomer in a two‐step method. In the first step, poly(amic acid–hydroxyamide) precursors were synthesized by low‐temperature solution polymerization in an organic solvent. Subsequently, the thermal cyclodehydration of the poly(amic acid–hydroxyamide) precursors at 350 °C produced the corresponding poly(imide–benzoxazole) copolymers. The inherent viscosities of the precursor polymers were around 0.19–0.33 dL/g. The cyclized poly(imide–benzoxazole) copolymers had glass‐transition temperatures in the range of 331–377 °C. The 5% weight loss temperatures ranged from 524 to 535 °C in nitrogen and from 500 to 514 °C in air. The poly(imide–benzoxazole) copolymers were amorphous, as evidenced by the wide‐angle X‐ray diffraction measurements. The structures of the precursor copolymers and the fully cyclized copolymers were characterized by Fourier transform infrared, ¹H NMR, and elemental analysis. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 6020–6027, 2005     

Perturbation analysis of finitely clad optical waveguides and couplers

In calculating the modal characteristics of a finitely clad optical waveguide, if the wavelength is much shorter than the core of the waveguide, then the cladding of the waveguide can be assumed to be infinite. On the other hand, if the wavelength is much longer than the core, the core can be ignored. These two approximations, although simple and accurate in the two respective extreme cases, do not provide adequate information in the transition region, where many tapered devices are operated. To overcome this a novel perturbation method is devised, in which these two approximations are combined in such a way that a result that is accurate in all cases can be obtained. Analytical expressions based on this method for describing the dispersion characteristics of finitely clad slab waveguides and circular step-index fibres are derived and compared with other conventional approximations. The combined use of this method and the coupled-mode theory for the analysis of optical couplers is also described.     

Hilbert空间中非扩张映象的最近的公共不动点的逼近问题

本文在Hilbert空间的框架下,研究无限族非扩张映象T_1,T_2,…的迭代程序x_n+1=λ_(n+1)y+(1-λ_(n+1))T_(n+1)x_n的收敛性问题．在适当的条件下,证明了该迭代序列收敛于这一非扩张映象族的最近的公共不动点．其结果改进和推广了引文中相应的结果．     

由数列定义的函数

We construct real valued functions from infinite sequences. We also consider some properties of such functions and null sequences.     

TMDIM: an improved algorithm for the structure prediction of transmembrane domains of bitopic dimers

\(\alpha\)-Helical transmembrane proteins are the most important drug targets in rational drug development. However, solving the experimental structures of these proteins remains difficult, therefore computational methods to accurately and efficiently predict the structures are in great demand. We present an improved structure prediction method TMDIM based on Park et al. (Proteins 57:577–585, 2004) for predicting bitopic transmembrane protein dimers. Three major algorithmic improvements are introduction of the packing type classification, the multiple-condition decoy filtering, and the cluster-based candidate selection. In a test of predicting nine known bitopic dimers, approximately 78% of our predictions achieved a successful fit (RMSD <2.0 Å) and 78% of the cases are better predicted than the two other methods compared. Our method provides an alternative for modeling TM bitopic dimers of unknown structures for further computational studies. TMDIM is freely available on the web at https://cbbio.cis.umac.mo/TMDIM. Website is implemented in PHP, MySQL and Apache, with all major browsers supported.     

IR,Raman, and Surface‐enhanced Raman Spectroscopic Study on Triruthenium Dipyridylamide Diruthenium Nickel Dipyridylamide Family: Metal‐metal Bonding and Structures

We report the infrared, Raman, and surface‐enhanced Raman scattering (SERS) spectra of triruthenium dipyridylamido complexes and of diruthenium mixed nickel metal‐string complexes. From the results of analysis on the vibrational modes, we assigned their vibrational frequencies and structures. The infrared band at 323–326 cm^?1 is assigned to the Ru₃ asymmetric stretching mode for [Ru₃(dpa)₄Cl₂]^0–2+. In these complexes we observed no Raman band corresponding to the Ru₃ symmetric stretching mode although this mode is expected to have substantial Raman intensity. There is no frequency shift in the Ru₃ asymmetric stretching modes for the complexes with varied oxidational states. No splitting in Raman spectra for the pyridyl breathing line indicates similar bonding environment for both pyridyls in dpa^– , thus a delocalized structure in the [Ru₃]^6–8+ unit is proposed. For Ru₃(dpa)₄(CN)₂ complex series, we assign the infrared band at 302 cm^?1 to the Ru₃ asymmetric stretching mode and the weak Raman line at 285 cm^?1 to the Ru₃ symmetric stretching. Coordination to the strong axial ligand CN^– weakens the Ru‐Ru bonding. For the diruthenium nickel complex [Ru₂Ni(dpa)₄Cl₂]^0–1+, the diruthenium stretching mode ν_Ru‐Ru is assigned to the intense band at 327 and 333 cm^?1 in the Raman spectra for the neutral and oxidized forms, respectively. This implies a strong Ru‐Ru metal‐metal bonding.