Stereoisomeric flavour compounds LXXIV: 2-phenylpropanol, 2-phenylpropanal and 2-phenylpropanal dimethyl acetal: structure elucidation and structure-function relationship

The direct enantioseparation of 2-phenylpropanol, 2-phenylpropanal and 2-phenylpropanal dimethyl acetal was achieved, using enantioselective gas chromatography and heptakis-[2,3-di-0-acetyl-6-0-tert.butyldimethylsilyl]--cyclodextrin (DIAC--CD) or octakis-[2,3-di-0-acetyl-6-0-tert.butyldimethylsilyl]--cyclodex-trin (DIAC--CD) as the chiral stationary phase. Their odour characteristics and threshold values were investigated by enantioselective gas chromatography/olfactometry. Starting from commercially available (R)-2-phenylpropionic acid, enantiopure (R)-configured reference compounds were synthesized.     

Ambipolar microcrystalline silicon thin-film transistors

Hydrogenated microcrystalline silicon (µc-Si:H) has recently received significant attention as a promising material for thin-film transistors (TFTs) in large area electronics due to its high electron and hole charge carrier mobilities. We report on ambipolar TFTs based on microcrystalline silicon prepared by plasma-enhanced chemical vapor deposition at temperature of 160 °C with high electron and hole charge carrier mobilities of 40 cm²/Vs and 10 cm²/Vs, respectively. The ambipolar microcrystalline silicon TFTs provide a simple route in realizing large area integrated circuits at low cost. The electrical characteristics of the ambipolar microcrystalline silicon TFTs will be described and the first results on ambipolar inverters will be presented. The influence of the ambipolar TFT characteristics on the performance of the inverter will be also discussed.     

精通碳管理 平衡可权衡因素，优化供应链管理效率

随着全球变暖,世界范围内关于减少温室气体排放的法规要求也日益严格。针对二氧化碳排放问题的很多机会存在于供应链管理之中,这迫使公司寻找新的方法来进行有效的碳管理;从采购和生产到配送和产品再生。供应链管理中的权衡不再只是关于成本．服务和质量,而是关于成本．服务．质量和碳排放。     

Intermediates in the Methanol-to-hydrocarbons (MTH) Reaction: A Gas Phase Study of the Unimolecular Reactivity of Multiply Methylated Benzenium Cations

In order to reach a deeper insight into the reaction mechanism of the zeolite catalyzed methanol to hydrocarbons reaction (MTH), the proposed reaction intermediates, i.e., a series of multiply methyl-substituted benzenium ions has been generated in the gas phase by chemical ionization. The fragmentations of the corresponding long-lived (metastable) ions have been investigated. While expulsion of H₂ dominates for the lower homologues, elimination of methane dominates for the higher homologues, accompanied by increasing amounts CH₃^·. Loss of larger fragments relevant to the MTH-reaction, in particular ethene, propene and even butene, is also observed in minor amounts. This latter finding is consistent with a proposed reaction cycle in the MTH reaction known as the paring mechanism, and the feasibility of this mechanism has thus been demonstrated. The metastable gas-phase ions studied here are considerably more energetic than those residing in a zeolite catalyst, but they were found to decompose with markedly higher selectivity towards alkenes as compared to those activated by collision-induced dissociation (CID).