Synthesis and characterization of diphenylaminodiphenyl stryl based alternating copolymers

Diphenylaminobiphenylated stryl based alternating copolymers with phenyl or fluorene, which were expected to have a terphenylene vinylene backbone containing an (N,N‐diphenylamino)biphenyl pendant and a phenyl/fluorene/phenylene vinylene backbone containing an (N,N‐diphenylamino)biphenyl pendant, were synthesized by a Suzuki coupling reaction. The obtained copolymers were confirmed with various types of spectroscopy. The alternating copolymers showed good hole‐injection properties because of their low oxidation potential and good solubility and high thermal stability with a high glass‐transition temperature. The alternating copolymers showed blue emissions because of the adjusted conjugation lengths; the maximum wavelength was 460 nm for poly{4,4′‐biphenylene‐α‐[4″‐(N,N′‐diphenylamino)diphenyl]vinylene‐alt‐5‐(2′‐ethylhexyloxy)‐2‐methoxybenzene} and 487 nm for poly{4,4′‐biphenylene‐α‐[4″‐(N,N′‐diphenylamino)diphenyl] vinylene‐alt‐9,9‐dihexylfluorene}. The maximum brightness of indium tin oxide/poly(3,4‐ethylene dioxythiophene)/polymer/LiF/Al devices with poly{4,4′‐biphenylene‐α‐[4″‐(N,N′‐diphenylamino)diphenyl]vinylene‐alt‐5‐(2′‐ethylhexyloxy)‐2‐methoxybenzene} or poly{4,4′‐biphenylene‐α‐[4″‐(N,N′‐diphenylamino)diphenyl]vinylene‐alt‐9,9‐dihexylfluorene} as the emitting layer was 250 or 1000 cd/m², respectively. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 341–347, 2007     

掺CdSxSe1-x玻璃波导分布反馈光学双稳器件

本文给出了掺CdS_xSe_1-x玻璃平面波导分布反馈(DFB)光学双稳器件的设计和制备方法,实现了低功耗、快速的本征光学双稳。     

Spontaneous formation of cadmium hydroxide nanostrands in water

Cadmium hydroxide nanostrands with a diameter of 1.9 nm were spontaneously formed by raising the pH of a dilute Cd(NO3)2 solution. The length reaches a few micrometers and the aspect ratio exceeds 1000. The crystallographic structure was successfully elucidated by high-resolution electron microscopy. The surface of the nanostrands was remarkably positively charged and adsorbed an astonishing number of negatively charged dye molecules.     

An Arc as the Inverse Limit of a Single Bonding Map of Type N on [0,1]

Let I = [0, 1], c ₁, c ₂ ∈ (0, 1) with c ₁ < c ₂ and f : I⊸I be a continuous map satisfying: are both strictly increasing and is strictly decreasing. Let A = {x ∈ [0, c ₁]∣f(x) = x}, a=max A, a ₁ =max(A\{a}), and B = {x ∈ [c ₂, 1]∣f(x) = x}, b=minB, b ₁ =min(B\{b}). Then the inverse limit (I, f) is an arc if and only if one of the following three conditions holds: (1) If c ₁ < f (c ₁) ≤ c ₂ (resp. c ₁ ≤ f (c ₂) < c ₂), then f has a single fixed point, a period two orbit, but no points of period greater than two or f has more than one fixed point but no points of other periods, furthermore, if A≠φ and B≠φ, then f (c ₂) > a (resp. f (c ₁) < b). (2) If f (c ₁) ≤ c ₁ (resp. f (c ₂) ≥ c ₂), then f has more than one fixed point, furthermore, if B≠φ and A\ {a} ≠φ, f (c ₂) ≥ a or if a ₁ < f (c ₂) < a, f ² (c ₂) > f (c ₂), (resp. f has more than one fixed point, furthermore, if A≠φ and B\{b}≠φ, f (c ₁) ≤ b or if b < f (c ₂) < b ₁, f ² (c ₁) < f (c ₁)). (3) If f (c ₁) > c ₂ and f (c ₂) < c ₁, then f has a single fixed point, a single period two orbit lying in I\(u, v) but no points of period greater than two, where u, v ∈ [c ₁, c ₂] such that f (u) = c ₂ and f (v) = c ₁. Supported by the National Natural Science Foundation of China (No. 19961001, No. 60334020) and Outstanding Young Scientist Research Fund. (No. 60125310)     

Molality as a unit of measure for expressing 1H MRS brain metabolite concentrations in vivo

Absolute concentrations of cerebral metabolite in in vivo 1H magnetic resonance spectroscopy studies (1H-MRS) are widely reported in molar units as moles per liter of tissue, or in molal units as moles per kilogram of tissue. Such measurements require external referencing or assumptions as to local water content. To reduce the scan time, avoid assumptions that may be invalid under specific pathologies, and provide a universally accessible referencing procedure, we suggest that metabolite concentrations from 1H-MRS measurements in vivo be reported in molal units as moles per kilogram of tissue water. Using internal water referencing, a two-compartment water model, a simulated brain spectrum for peak identification, and a spectroscopic bi-exponential spin-spin relaxation segmentation technique, we measured the absolute concentrations for the four common 1H brain metabolites: choline (Cho), myo-inositol (mIno), phosphocreatine + creatine (Cr), and N-acetyl-aspartate (NAA), in the hippocampal region (n = 26) and along the Sylvian fissure (n = 61) of 35 healthy adults. A stimulated echo localization method (20 ms echo time, 10 ms mixing time, 4 s repetition time) yielded metabolite concentrations, uncorrected for metabolite relaxation or contributions from macromolecule resonances, that were expectantly higher than with molar literature values. Along the Sylvian fissure the average concentrations (coefficient of variation (CV)) in mmoles/kg of tissue water were 17.6 (12%) for NAA, 14.2 (9%) for Cr, 3.6 (13%) for Cho, and 13.2 (15%) for mIno. Respective values for the hippocampal region were 15.7 (20%), 14.7 (16%), 4.6 (19%), and 17.7 (26%). The concentrations of the two regions were significantly different (p 相似文献   

Lipase TL-mediated kinetic tesolution of 5-benzyloxy-1-tert-butyldimethylsilyloxy-2-pentanol at low temperature: concise asymmetric synthesis of both enantiomers of a piperazic acid derivative

Lipase TL-mediated kinetic resolution of (+/-)-5-benzyloxy-1-tert-butyldimethylsilyloxy-2-pentanol (5) at low temperature proceeded to give the corresponding (S)-alcohol 5 and (R)-acetate 6 in quantitative yields with high enantiomeric purity. The addition of bases such as pyridine, DMAP, 2,4- and 2,6-lutidines, or triethylamine considerably enhanced the rate of kinetic resolution. The alcohol (S)-5 and the acetate (R)-6 were converted to piperazic acid derivatives (R)- and (S)-3, respectively, via the intramolecular Mitsunobu reaction as a key step.     

Synthesis of a new insoluble polymer-supported chiral alcohol auxiliary and its first application to nucleophilic addition to ketenes

The preparation of a new optically active alcohol with a carboxylic function that allowed its attachment to an amine-functionalized insoluble polymer is described. Its first use as a polymer supported chiral auxiliary is demonstrated by asymmetric transformation of two racemic aryl propionic acids via ketene formation (95-96% ee).     

激光器机理及激光功率表达式的实验验证

运用光反馈的原理和技术演示并验证激光功率表达式，说明激光介质和光学谐振腔的性质和作用。     

β-NMR in II–VI semiconductors

β-active probe nuclei are implanted in nominally undoped ZnSe crystals. β-radiation detected nuclear magnetic resonance (β-NMR) studies are described for two different probe nuclei, ⁸Li and ¹²B. This way, the implantation behavior of two “opposite”dopants, one acceptor (Li) and one donor (B) can be characterized by the same microscopic technique. Such characterizations are attempted in terms of the structure of intermediate or final lattice sites, defect charge states, or the kinetics of defect reactions and site changes. This revised version was published online in July 2006 with corrections to the Cover Date.