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941.
Fen Tan Cong Xiao Hong‐Gang Cheng Wei Wu Ke‐Rong Ding Prof. Dr. Wen‐Jing Xiao 《化学:亚洲杂志》2012,7(3):493-497
942.
Cheng‐Xiong Liu Zhi‐yong Guo Yan‐Hong Xue Hong‐Yan Zhang Hong‐Qi Zhang Kun Zou Nian‐Yu Huang 《Magnetic resonance in chemistry : MRC》2012,50(4):320-324
Three new steroidal compounds with polyhydroxy groups, tupisteroide A–C (1–3), were obtained from the roots of Tupistra chinensis, together with one known compound (4) that was isolated from this plant for the first time. The structures of tupisteroide A–C were determined on the basis of one‐ and two‐dimensional NMR spectroscopy, including 1H–1H Correlation Spectroscopy, Heteronuclear Multiple Bond Correlation, and Heteronuclear Single Quantum Coherence experiments. The isolated compounds were evaluated for their cytotoxic activities against A549, HepG2, and CaSki cancer cell lines in vitro. Among them, compounds 1, 2, and 4 did not show significant inhibitory activity, but compound 3 showed cytotoxicity against A549 cancer cell lines with IC50 values of 25.0 μM. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
943.
Jie Miao Weiwei He Lifen Zhang Yi Wang Zhenping Cheng Xiulin Zhu 《Journal of polymer science. Part A, Polymer chemistry》2012,50(11):2194-2200
In this work, living radical polymerizations of a water‐soluble monomer poly(ethylene glycol) monomethyl ether methacylate (PEGMA) in bulk with low‐toxic iron catalyst system, including iron chloride hexahydrate and triphenylphosphine, were carried out successfully. Effect of reaction temperature and catalyst concentration on the polymerization of PEGMA was investigated. The polymerization kinetics showed the features of “living”/controlled radical polymerization. For example, Mn,GPC values of the resultant polymers increased linearly with monomer conversion. A faster polymerization of PEGMA could be obtained in the presence of a reducing agent Fe(0) wire or ascorbic acid. In the case of Fe(0) wire as the reducing agent, a monomer conversion of 80% was obtained in 80 min of reaction time at 90 °C, yielding a water‐soluble poly(PEGMA) with Mn = 65,500 g mol?1 and Mw/Mn = 1.39. The features of “living”/controlled radical polymerization of PEGMA were verified by analysis of chain‐end and chain‐extension experiments. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
944.
Shijing Cheng Mingqiang Zhang Tianyu Wu Sean T. Hemp Brian D. Mather Robert B. Moore Timothy E. Long 《Journal of polymer science. Part A, Polymer chemistry》2012,50(1):166-173
Copolymers of n‐butyl acrylate and phosphonium ionic liquid monomers possessing various alkyl substituents and counterions were synthesized through a combination of conventional free radical copolymerization and anion exchange. Differential scanning calorimetry and dynamic mechanical analysis provided the thermal and mechanical properties of these phosphonium cation‐containing random copolymers. Factors including alkyl chain length of phosphonium substituents, counterion type, as well as ionic concentration significantly influenced the association of phosphonium cations. Phosphonium ionomers with trialkyl substituents on phosphonium cations did not display the characteristic small‐angle X‐ray scattering peak, suggesting the absence of ionic clusters. However, low q peaks in wide‐angle X‐ray diffraction was indicative of significant concentration fluctuations wherein the ionic monomeric units associated. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
945.
946.
947.
948.
Niu Xiping Cheng XiaomanXu Jianping Zhang XiaosongXuan Rongwei Wu YanyuLi Lan 《Superlattices and Microstructures》2012
This study reports a simple method for the synthesis of different size of wurtzite ZnO nanoparticles in assistance of tetraethyl orthosilicate (TEOS). With the increase of the amount of TEOS added, the average size of ZnO nanoparticles was found decreased from ∼14.6 to ∼1.9 nm by characterization of X-ray diffraction (XRD) and high-resolution electron microscopy (HRTEM). The growth of ZnO nanoparticles is proposed to be controlled by the density of the SiO2 chain mesh which is determined by TEOS amount in precursor. Ultraviolet–visible (UV–VIS) absorption and photoluminescence (PL) spectra show both shift to higher energy in cut-off edge and in visible emission bands respectively. The electron transition process in the mechanism of the visible emission shift was described and related to quantum size effect in ZnO nanoparticles. 相似文献
949.
A series of fluorinated fullerene-fused 1,3-dioxolanes have been facilely and efficiently synthesized in the presence of easily available LiClO4·3H2O. The influences of the number of fluoro-substituents and their positions linked to the phenyl ring on the isolated yield of fullerene-fused 1,3-dioxolanes have been studied in detail. Based on reaction facts, a possible reaction mechanism for the formation of fluorinated fullerene-fused 1,3-dioxolanes has been proposed. Furthermore, detailed ultraviolet absorption spectra, fluorescence emission spectra, and cyclic voltammogram further explain the optical properties and electronic transmission capabilities of the products. 相似文献
950.
Chunhui Dai Yuxiang Wang Yiwu Quan Qingmin Chen Yixiang Cheng Chengjian Zhu 《Journal of polymer science. Part A, Polymer chemistry》2014,52(21):3080-3086
The β‐diketonate‐based achiral polymer P‐1 could be synthesized by the polymerization of 3,7‐dibromo‐2,8‐dimethoxy‐5,5‐dioctyl‐5H‐dibenzo[b,d]silole ( M1 ) with (Z)?1,3‐bis(4‐ethynylphenyl)?3‐hydroxyprop‐en‐1‐one ( M2 ) via typical Sonogashira coupling reaction. The β‐diketonate unit in the main chain backbone of P‐1 can further coordinate with Eu(TTA)x [TTA? = 4,4,4‐trifluoro‐1‐(thiophen‐2‐yl)butane‐1,3‐dionate anion, X = 1, 2, 3] to afford corresponding Eu(III)‐containing polymer complexes. The resulting achiral polymer complex P‐2 (X = 2) can exhibit strong circular dichroism (CD) response toward both N‐Boc‐l and d‐ proline enantiomers. The CD signal was preliminarily attributed to coordination induction between chiral N‐Boc‐proline and the Eu(III) complex moiety. The linear regression analysis of CD sensing shows a good agreement between the magnitude of molar ellipticity and concentration of chiral N‐Boc‐l or d‐ proline, which indicates this kind Eu(III)‐containing achiral polymer complex can be used as a chiral probe for enantioselective recognition of N‐Boc‐l or d‐ proline enantiomers based on Cotton effect of CD spectra. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 3080–3086 相似文献