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971.
Ying Lin Teng‐Ling Ye Yu Chen Dong‐Ge Ma Zhi‐Kuan Chen Yan‐Feng Dai Yong‐Xi Li 《Journal of polymer science. Part A, Polymer chemistry》2010,48(24):5930-5937
A new bipolar conjugated polyfluorene copolymer with triphenylamine and cyanophenylfluorene as side chains, poly{[9,9‐di(triphenylamine)fluorene]‐[9,9‐dihexyl‐fluorene]‐[2,7‐bis(4′‐cyanophenyl)‐9,9′‐spirobifluorene]} ( PTHCF ), was synthesized for studying the polymer backbone emission. Its absolute weight‐average molecular weight was determined as 4.85 × 104 by using gel permeation chromatography with a multiangle light scattering detector. In contrast to the electronic absorption spectrum in dilute solution, the absorbance of PTHCF in thin film was slightly blue shifted. By comparison of the solution and thin‐film photoluminescence (PL) spectra, a red shift of Δλ = 8–9 nm was observed in the thin‐film PL spectrum. The HOMO and LUMO energy levels of the resulting polymer were electrochemically estimated as ?5.68 and ?2.80 eV, respectively. Under the electric‐field intensity of 4.8 × 105 V cm?1, the obtained hole and electron mobilities were 2.41 × 10?4 and 1.40 × 10?4 cm2 V?1 s?1, respectively. An electroluminescence device with configuration of ITO/PEDOT:PSS/ PTHCF 70%+PBD30%/CsF/Ca/Al exhibited a deep‐blue emission as a result of excitons formed by the charges migrating along the full‐fluorene main chain. The incorporation of the bipolar side chains into the polymer structure prevented the intermolecular interaction of the fluorene moieties, balance charge injection/transport, and thereby improve the polymer backbone emission. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 相似文献
972.
Enantioselective addition of diethylzinc to a series of aromatic aldehydes was developed using a modular amino acid amide chiral ligand (2S)‐3‐phenyl‐N‐((R)‐1‐phenyl‐ethyl)‐2‐(tosylamino)propanamide without using titanium complex. The catalytic system employing 10 mol% of 1g was found to promote the addition of diethylzinc (ZnEt2) to a wide range of aromatic aldehydes with electron‐donating and electron‐withdrawing substituents, giving up to 82% ee of the corresponding secondary alcohol under mild conditions. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
973.
Zicong Jian Yuying Pu Jianzhang Fang Zhiping Ye 《Photochemistry and photobiology》2010,86(5):1016-1021
Microemulsion is the easiest and cleanest of the popular methods of synthesizing nanomaterial. This work synthesized the nanosized La-TiO2 and Ce-TiO2 particles through the hydrolyzation of tetrabutyl titanate in a Triton X-100/n-hexanol/cyclohexane/water reverse microemulsion. The particles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform-infrared spectroscopy (FT-IR) and thermogravimetry (TG). The photocatalytic activity was evaluated by photocatalytic degradation of methyl orange (MO) under ultraviolet light and visible light irradiation. The results showed that reverse microemulsion produced the nanosized and well-separated particles, which are obviously in degrading MO. Comparing the pure TiO2 with doping TiO2, the doping ones are smaller and have better photocatalytic activity, which was best at the molar content of 0.1% for La, whereas for Ce it was 0.5%. 相似文献
974.
975.
Lu Liu Mingde Ye Xingen Hu Xiaochun Yu Lixue Zhang Xinxiang Lei 《Tetrahedron: Asymmetry》2011,22(16-17):1667-1671
A series of chiral salen C2-symmetric aminophenols 1–4, which were derived from (1R,2R)- or (1S,2S)-1,2-diphenylethane-1,2-diamine with the corresponding salicylic aldehyde through a [2+2] condensation reaction, have been prepared. The NMR studies demonstrated that they can function as chiral solvating agents for the determination of the enantiomeric purity of chiral carboxylic acids. 相似文献
976.
977.
A method based on MCE coupled with chemiluminescence (CL) detection was developed for the determination of taurine (Tau) and amino acids including alanine (Ala), glycine (Gly), tryptophan (Trp), glutamic acid (Glu) and aspartic acid (Asp) present in mice single fibrosarcoma (S180) cells. Cell injection, loading, cytolysis, electrophoretic separation and CL detection were integrated onto a simple double‐T microfluidic chip. The intracellular constituents were electrophoretically separated within 150 s. The CL detection was based on the enhancement effects of Tau and amino acids on the CL reaction of luminol with H2O2 and Cu2+. The average amounts of Tau, Trp, Gly, Ala, Glu and Asp in per S180 cell from a cell population were 4.73, 1.23, 2.65, 1.94, 1.61 and 1.99 fmol. Ten S180 cells were analyzed, and the contents of Tau, Trp, Gly, Ala, Glu and Asp in mice single S180 cells were found to be in the range of 1.78–8.84, 0.95–2.31, 1.08–6.87, 1.03–4.05, 0.84–2.61 and 0.82–3.68 fmol, respectively. This work demonstrates that MCE coupled with CL detection is a useful analytical tool that is simple, quick and highly sensitive for single‐cell analysis. 相似文献
978.
979.
Miao Hong Li Pan Wei‐Ping Ye Dong‐Po Song Yue‐Sheng Li 《Journal of polymer science. Part A, Polymer chemistry》2010,48(8):1764-1772
The copolymerizations of ethylene with cyclic dienes [dicyclopentadiene (DCPD) and 2,5‐norbornadiene (NBD)] using bis(β‐enaminoketonato)titanium complexes [PhN = C(R2)CHC(R1)O]2TiCl2 ( 1a : R1 = CF3, R2 = CH3; 1b : R1 = t‐Bu, R2 = CF3; 1c : R1 = Ph, R2 = CF3) have been investigated. In the presence of modified methylaluminoxane, these complexes exhibited high catalytic activities in the copolymerization of ethylene with DCPD or NBD, affording high molecular weight copolymers with unimodal molecular weight distributions. 1H and 13C‐NMR spectra reveal ethylene/DCPD copolymerizations by catalysts 1a – c proceeds through the enchainment of norbornene ring. Catalysts 1a and 1c showed a tendency to afford alternating copolymers. More noticeably, catalysts 1b and 1c bearing bulky substituents on the ligands promote ethylene/NBD copolymerization without crosslinking, affording the copolymer containing intracyclic double bonds. The NBD incorporation as high as 27.2 mol % has been achieved by catalyst 1c . Moreover, the microstructures of the copolymers were further confirmed by the measurement of reactivity ratios and dyad monomer sequences as well as mean sequence lengths. The intracyclic double bonds of ethylene/DCPD or ethylene/NBD copolymers can be fully converted into polar groups such as epoxy, amine, silane, and hydroxyl groups under mild conditions. Convenient synthesis of hydroxylated polyethylene can be provided for the first time through the ring opening reaction of epoxide. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1764–1772, 2010 相似文献
980.