5-(对羧基苯偶氮)-8-羟基喹啉与钍的显色反应及应用

研究了钍与5-(对羧基苯偶氮)-8-羟基喹啉(5-CPAHQ)的显色反应条件:在阳离子表面活性剂十六烷基三甲基溴化铵(CTMAB)存在下,pH4.4-5.4缓冲介质中,形成稳定的橙红色络合物,最大吸收波长为490nm,ε=1.10×105L·mol-1·cm-1,钍在0-9μg/25mL范围内符合比尔定律。用TBP萃淋树脂分离,该方法可用于测定矿石中的微量钍。     

An algorithm for three-way data analysis that alternatively minimizes coupled vector (COV) resolution error and PARAFAC error.

A novel algorithm, alternatively minimizing coupled vector (COV) resolution error and PARAFAC error algorithm, is proposed in this paper. This algorithm can overcome the problem of slow convergence and is insensitive to the estimation of component number, such problems are unavoidable while using the traditional parallel factors analysis (PARAFAC) algorithm. In other words, this algorithm is capable of improving the computing speed and providing accurate resolutions provided that the number of factors used in the computation is no less than that of the actual underlying ones. The characteristic performances were demonstrated with a novel fluorescence data array.     

ANTI FUZZY VECTOR SPACES（Ⅱ）

ＡＮＴＩＦＵＺＺＹＶＥＣＴＯＲＳＰＡＣＥＳ（Ⅱ）ＣｈｅｎＹｏｎｇｎｉａｎ（ＤｅｐａｒｔｍｅｎｔｏｆＭａｔｈｅｍａｔｉｃｓ，ＸｉｎｊｉａｎｇＮｏｒｍａｌＵｎｉｖｅｒｓｉｔｙ，８３００５４，Ｘｉｎｊｉａｎｇ，Ｐ．Ｒ．Ｃｈｉｎａ）ＡＮＴＩＦＵＺＺＹＶＥＣＴ...     

Synthesis and transition temperatures of liquid crystals incorporating a 1,4-tetrafluorophenylene unit

Two homologous series of mesogenic materials which incorporate a 1,4-tetrafluorophenylene moiety and a terminal cyano- or nitro-substituent have been synthesized by using palladiumcatalysed coupling procedures. The compounds exhibit nematic and/or smectic A phases.     

Adams谱序列中α~s(n)h0hk的收敛性

证明了(i)在p≥ 5,2≤s≤p- 1 ,k≥ 2时, β_sh₀h_k+1收敛到E_∞ ;(ii)在p≥7,3≤s≤p-1,k≥3时, γ_sh₀h_k+1收敛到E_∞.     

Viscosity-splitting scheme for the Navier-Stokes equations

A viscosity-splitting scheme for the initial boundary value problems of the Navier-Stokes equations is considered. In the scheme, the Stokes equation is solved in conjunction with a nonhomogeneous boundary condition which connects the tangent flow with a no-slip flow. Convergence is proved.     

Continuous preparation of decorated nano zinc oxide organic sols with intense luminescence

A sort of decorated nano ZnO organic sols have been successively prepared by pulsed laser ablation at the interface of ZnO target and a flowing liquid containing polymers. It is found that the decorated nano ZnO ethanol sols, the decorated nano ZnO-PS (polystyrene) cyclohexane sols and the decorated nano ZnO-PMMA (polymethyl methacrylate) ethyl butyrate sols all have strong fluorescence emission at 329 nm and 411 nm, 308 nm and 317 nm, and at 330 nm and 400 nm, respectively. The results show the decorating for nano ZnO will intensely affect their luminescence, and the wavelength and intensity of luminescence can be adjusted or controlled by the different decoration.     

Synthesis of grafted poly(p‐phenyleneethynylene) with energy donor–acceptor architecture via atom transfer radical polymerization: Towards nonaggregating and hole‐facilitating light‐emitting material

In this contribution, we demonstrate a new effective methodology for constructing highly efficient and durable poly(p‐phenyleneethynylene) (PPE) containing emissive material with nonaggregating and hole‐facilitating properties through the introduction of hole‐transporting blocks into the PPE system as the grafting coils as well as building the energy donor–acceptor architecture between the grafting coils and the PPE backbone. Poly(2‐(carbazol‐9‐yl)ethyl methacrylate) (PCzEMA), herein, is chosen as the hole‐transporting blocks, and incorporated into the PPE system as the grafting coils via atom transfer radical polymerization. The chemical structure of the resultant copolymer, PPE‐g‐PCzEMA, was characterized by NMR and gel permeation chromatography, showing that the desirable copolymer was obtained with the narrow polydispersity. The increased thermal stability of PPE‐g‐PCzEMA was confirmed by thermogravimetric analysis and differential scanning calorimetry along with its macroinitiator. The optoelectronic properties of this copolymer were studied in detail by ultraviolet‐visible absorption, photoluminescence emission and excitation spectra, and cyclic voltammogram (CV). The results indicate that PPE‐g‐PCzEMA exhibits the solid‐state luminescent property dominated by individual lumophores, and also the energy transfer process from the PCzEMA blocks to the PPE backbone with a relatively higher energy transfer efficiency in the solid‐state compared to that of the solution state. Additionally, the hole‐injection property is greatly facilitated due to the presence of PCzEMA, as confirmed by CV profiles. All these data indicate that PPE‐g‐PCzEMA is a good candidate for use in optoelectronic devices. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 3776–3787, 2007