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111.
Summary This study describes the optimization of microextraction as a method for extracting volatile compounds from wine. The study
has been applied to twelve compounds present in wine: 3-methylbutyl acetate, 3-methyl-1-butanol, ethyl hexanoate, hexanol,
ethyl octanoate, butanoic acid, ethyl decanoate, diethyl succinate, hexanoic acid, phenylethanol, octanoic acid, and decanoic
acid. These compounds were selected from those identified by GC-MS analysis of a real wine sample.
By means of a synthetic wine, the study investigated the influence on extraction yield of the solvents and salts used, the
proportion of salts, and the agitation time. The determination was performed by GC with flame ionization detection and an
internal standard was used for quantification. The method was applied to samples of white wine from La Rioja. 相似文献
112.
Sang‐Mi Park Kyoung‐Soo Yook Woo‐Hyung Lee Yongtaek Hong Jun‐Yeob Lee In‐Nam Kang 《Journal of polymer science. Part A, Polymer chemistry》2013,51(23):5111-5117
Two new thermally crosslinkable hole‐transporting polymers, X‐PTPA and X‐PCz, were synthesized via Yamamoto coupling reactions. The number‐averaged molecular weights (Mn) of X‐PTPA and X‐PCz were found to be 45,000 and 48,000, respectively, and therewith, polydispersity indices were of 1.8 and 1.7, respectively. Thermally crosslinked X‐PTPA and X‐PCz exhibit excellent solvent resistance and stable optoelectronic properties. The UV–visible maximum absorption peaks of X‐PTPA and X‐PCz in the thin film state are at 389 and 322 nm, respectively. The HOMO levels of X‐PTPA and X‐PCz are estimated to be ?5.27 and ?5.39 eV, respectively. Multilayered devices (ITO/crosslinked X‐PTPA or X‐PCz/SY‐PPV/LiF/Al) were fabricated with SY (SuperYellow) as the emitting layer. The maximum efficiency of the multilayered device with a crosslinked X‐PTPA layer is approximately three times higher than that of the device without a crosslinked X‐PTPA layer and much higher than that of the crosslinked X‐PCz device. This result can be explained by the observations that crosslinked X‐PTPA produces increased electron accumulation within the emitter, SY, and also efficient exciton formation due to improved charge balance. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 5111–5117 相似文献
113.
Aurica Farcas Silvia Janietz Valeria Harabagiu Philippe Guegan Pierre‐Henri Aubert 《Journal of polymer science. Part A, Polymer chemistry》2013,51(7):1672-1683
Polyfluorene PF?γCD rotaxane copolymer, composed of randomly distributed 9,9‐dioctylfluorene, methyltriphenylamine (electron‐donating) and 9‐dicyanomethylenefluorene complexed with γ‐cyclodextrin (γCD) (electron‐accepting) structural units, has been synthesized by Suzuki cross‐coupling reaction. The chemical structures were proved by FTIR and 1H NMR spectroscopy. The surface morphology, thermal, optical, electrochemical behavior, and adhesion characteristics of the obtained rotaxane copolymer have been investigated and compared with those of the nonrotaxane counterpart ( PF ). Relatively high fluorescence efficiency, almost identical normalized absorbance maximum in solution and solid‐state of PF?γCD rotaxane copolymer, and a more uniform and smoother surface with lower adhesion forces provides the role of γCD encapsulation on the lower aggregation propensity. PF?γCD and PF copolymers exhibit n‐ and p‐doping processes and blue‐light emission in the film state. The optical and electrochemical band gaps (ΔEg), as well as the highest occupied molecular orbital/lowest unoccupied molecular orbital positions in an energetic diagram indicate that both copolymers are promising blue‐emitting electroluminescent materials. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
114.
115.
Copolyphenylenes with pendant benzimidazolyl and diethanolaminohexyloxy groups: Synthesis and electron‐transporting application in PLEDs 下载免费PDF全文
Chih‐Yang Tseng Wen‐Fen Su Yun Chen 《Journal of polymer science. Part A, Polymer chemistry》2017,55(15):2494-2505
Two new electron‐transporting copolyphenylenes P1NH and P2NH possessing balanced charges crucial to emission efficiency of polymer light‐emitting diodes (PLEDs) have been synthesized and applied as an electron‐transporting layer (ETL). The main chain structure is all para‐linkage for P1NH and both para‐ and meta‐linkage for P2NH , with the same pendant electron‐withdrawing benzimidazolyl and polar diethanolaminohexyloxy groups. Both copolymers possess excellent thermal stability (T d > 300 °C, T g > 100 °C) due to their rigid backbones. In addition, the pendant groups effectively lower LUMO (~ ?2.70 eV) and HOMO (~ ?5.70 eV) levels, resulting in improved electron‐transporting and hole‐blocking capabilities. Multilayer yellow‐emitting PLEDs with a configuration of ITO/PEDOT:PSS/SY/ETL/LiF/Al were successfully fabricated by the spin‐coating process. The maximum luminance and maximum current efficiency of the P1NH ‐based device were 12,881 cd/m2 and 10.94 cd/A, respectively, superior to the performance of P2NH ‐based device (4938 cd/m2, 3.70 cd/A) and the device without ETL (8690 cd/m2, 2.78 cd/A). Current results indicate that P1NH is highly effective in enhancing electron transport and device performance. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55 , 2494–2505 相似文献
116.
Min Ju Cho U Ra Lee Youn Sun Kim Jicheol Shin Young Min Kim Young Wook Park Byeong‐Kwon Ju Jung‐Il Jin Dong Hoon Choi 《Journal of polymer science. Part A, Polymer chemistry》2010,48(9):1913-1918
A functionalized deoxyribonucleic acid (Cz‐DNA) was prepared with carbazolyl ammonium lipid as a triplet host material for phosphorescent material system. It is soluble in organic solvents, which facilitates the sample preparation for the absorption and luminescent properties in solid states. A highly soluble iridium complex, Ir(Cz‐ppy)3 with carbazolyl‐substituted 2‐phenylpyridine ligands was employed for studying the phosphorescence in Cz‐DNA. There is a good overlap between the photoluminescence spectrum of Cz‐DNA and the metal‐to‐ligand charge transfer (MLCT) absorption bands of the iridium complex. This overlap enables efficient energy transfer from the excited state in the host to the MLCT band of Ir(Cz‐ppy)3. In addition, photoluminescence quantum yield of Cz‐DNA was found to be relatively larger than the copolymer (PCzSt) with vinylcarbazole and styrene. Thus, Cz‐DNA was employed as a triplet host material for fabricating multilayered electrophosphorescence devices via modification of its property by doping 5,4‐tert‐butylhexyl‐1,3,4‐oxadiazole (PBD). After doping 30 wt % PBD and 10 wt % Ir(Cz‐ppy)3 into Cz‐DNA, we achieved much improvement in electron injection/transport from an adjacent carrier transport layer, resulting in much improved device performances. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1913–1918, 2010 相似文献
117.
Low coherence multiple-quantum well edge-emitting light-emitting diodes were obtained using selective-area metalorganic vapor-phase
epitaxial growth, which utilized growth rate enhancement on an open stripe region between mask stripes. An optical absorption
region, which was controlled by selective-area growth, was introduced to suppress optical feedback. At a driving current of
100 mA and an ambient temperature of 25°C, a power of 55 μW was coupled into a single-mode fiber, and a broad spectrum without
spectral ripple was observed. Low coherence characteristics and very small temperature dependence were obtained in the temperature
range from -40°C to 85°C. The modulation bandwidth was 210 MHz at a bias current of 100 mA. 相似文献
118.
Bar‐Yuan Hsieh Kun‐Ming Yeh Yun Chen 《Journal of polymer science. Part A, Polymer chemistry》2005,43(21):5009-5022
New copoly(aryl ether)s ( P1 – P3 ) containing alternate 2,5‐dihexyloxy‐1,4‐di(m‐ethoxystyryl)benzene ( P1 , P2 ) or 2,5‐dihexyloxy‐1,4‐distyrylbenzene ( P3 ) chromophores and aromatic 1,3,4‐oxadiazole ( P1 ) or 3,3″‐terphenyldicarbonitrile ( P2 , P3 ) segments were prepared by Horner reaction ( P1 and P2 ) or nucleophilic displacement reaction ( P3 ). They are basically amorphous materials with 5% weight‐loss temperature above 410 °C. Their absorption, photoluminescence spectra, and quantum yields are dependent on the composition of the isolated fluorophores. The emissions are exclusively dominated by 1,4‐distyrylbenzene segments via excitation energy transfer from electron‐transporting 1,3,4‐oxadiazole ( P1 ) or 3,3″‐terphenyldicarbonitrile ( P2 , P3 ) chromophores. The HOMO and LUMO energy levels have been estimated from their cyclic voltammograms, and the observations confirm that oxidation and reduction start from the emitting 1,4‐distyrylbenzene and electron‐transporting segments, respectively, indicating that both carriers affinity can be enhanced simultaneously. Among the two‐layer PLED devices (ITO/PEDOT/ P1 – P3 /Al), P1 exhibits the best performance with a turn‐on field of 4 × 105 V/cm and a maximum luminance of 225 cd/m2. However, P2 emits green–yellow light (555 nm), owing to the excimer emission. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5009–5022, 2005 相似文献
119.
Xiaoming Wu Yulin Hua Zhaoqi Wang Jiajin Zheng Shougen Yin Jiachun Deng Kongwu Wu Songliu Feijian Zhu Xia Niu 《Optik》2006,117(8):373-376
A bright white organic light-emitting diode (OLED) has been successfully fabricated in which a greenish-white emitting host Bis-(2-(2-hydroxyphenyl) benzothiazole)zinc (Zn(BTZ)2) is doped with an orange-red fluorescent dye 5,6,11,12-tetraphenylnaphthacene (rubrene). The pure white light emission with CIE coordinates of (0.341, 0.334) is achieved at the driving voltage of 20 V, and the corresponding luminance and external quantum efficiency are 4000 Cd/m2 and 0.63%. On the other hand, the pure red, green, and blue (RGB) emissions are obtained from the white OLED combined well with RGB custom-built optical color filters (CFs) with peaks at 616, 556, and 456 nm, respectively. Moreover, based upon the color mixture principles, we build a model of multi-color display mixed by the pure RGB emissions under the controllable bias. 相似文献
120.
Jaemin Lee Byung‐Jun Jung Sang Kyu Lee Jeong‐Ik Lee Hoon‐Je Cho Hong‐Ku Shim 《Journal of polymer science. Part A, Polymer chemistry》2005,43(9):1845-1857
We report here the synthesis via Suzuki polymerization of two novel alternating polymers containing 9,9‐dioctylfluorene and electron‐withdrawing 4,4′‐dihexyl‐2,2′‐bithiazole moieties, poly[(4,4′‐dihexyl‐2,2′‐bithiazole‐5,5′‐diyl)‐alt‐(9,9‐dioctylfluorene‐2,7‐diyl)] (PHBTzF) and poly[(5,5′‐bis(2″‐thienyl)‐4,4′‐dihexyl‐2,2′‐bithiazole‐5″,5″‐diyl)‐alt‐(9,9‐dioctylfluorene‐2,7‐diyl)] (PTHBTzTF), and their application to electronic devices. The ultraviolet–visible absorption maxima of films of PHBTzF and PTHBTzTF were 413 and 471 nm, respectively, and the photoluminescence maxima were 513 and 590 nm, respectively. Cyclic voltammetry experiment showed an improvement in the n‐doping stability of the polymers and a reduction of their lowest unoccupied molecular orbital energy levels as a result of bithiazole in the polymers' main chain. The highest occupied molecular orbital energy levels of the polymers were ?5.85 eV for PHBTzF and ?5.53 eV for PTHBTzTF. Conventional polymeric light‐emitting‐diode devices were fabricated in the ITO/PEDOT:PSS/polymer/Ca/Al configuration [where ITO is indium tin oxide and PEDOT:PSS is poly(3,4‐ethylenedioxythiophene) doped with poly(styrenesulfonic acid)] with the two polymers as emitting layers. The PHBTzF device exhibited a maximum luminance of 210 cd/m2 and a turn‐on voltage of 9.4 V, whereas the PTHBTzTF device exhibited a maximum luminance of 1840 cd/m2 and a turn‐on voltage of 5.4 V. In addition, a preliminary organic solar‐cell device with the ITO/PEDOT:PSS/(PTHBTzTF + C60)/Ca/Al configuration (where C60 is fullerene) was also fabricated. Under 100 mW/cm2 of air mass 1.5 white‐light illumination, the device produced an open‐circuit voltage of 0.76 V and a short‐circuit current of 1.70 mA/cm2. The fill factor of the device was 0.40, and the power conversion efficiency was 0.52%. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1845–1857, 2005 相似文献