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181.
182.
We consider an order acceptance and scheduling model with machine availability constraints. The manufacturer (machine) is assumed to be available to process orders only within a number of discontinuous time intervals. To capture the real-life behavior of a typical manufacturer who has restrictions of time availability to process orders, our model allows the manufacturer to reject or outsource some of the orders. When an order is rejected or outsourced, an order-dependent cost of penalty will occur. The objective is to minimize the makespan of all accepted orders plus the total penalty of all rejected/outsourced orders. We study the approximability of the model and some of its important special cases. 相似文献
183.
Fang Su Yunlin Yang Yiyi Ou Dr. Weijie Zhou Dr. Fengkai Ma Dr. Jianhui Zhang Prof. Mikhail G. Brik Prof. Hongbin Liang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(30):e202200381
Eu2+-, Mn2+- and Eu2+−Mn2+-doped CaMgSi2O6 phosphors have been prepared by a high-temperature solid-state reaction. Systematic investigation of the concentration- and temperature-dependent luminescence of Mn2+ showed that Mn2+ ions occupy two distinct sites in CaMgSi2O6. Electron–vibration interaction (EVI) analyses of Mn2+ ions revealed Huang–Rhys factors of 4.73 and 2.82 as well as effective phonon energies of 313 and 383 cm−1 for the two sites. Eu2+−Mn2+ energy transfer is also discussed, and its efficiency is estimated by lifetime and luminescence spectra. The different thermal quenching behaviours of Eu2+ and Mn2+, the distinct emission colours of Eu2+ (blue, band peak at ∼451 nm) and Mn2+ (yellow–red range, band peaks at ∼583 and 693 nm) endow the co-doped samples with potential applications in luminescence thermometry and temperature-/excitation wavelength-responsive dual anti-counterfeiting. 相似文献
184.
Dr. Mykhaylo Dukh Walter A. Tabaczynski Sairaman Seetharaman Dr. Zhongping Ou Prof. Dr. Karl M. Kadish Prof. Dr. Francis D'Souza Prof. Dr. Ravindra K. Pandey 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(65):14996-15006
A series of chlorin-bacteriochlorin dyads (derived from naturally occurring chlorophyll-a and bacteriochlorophyll-a), covalently connected either through the meso-aryl or β-pyrrole position (position-3) via an ester linkage have been synthesized and characterized as a new class of far-red emitting fluorescence resonance energy transfer (FRET) imaging, and heavy atom-lacking singlet oxygen-producing agents. From systematic absorption, fluorescence, electrochemical, and computational studies, the role of chlorin as an energy donor and bacteriochlorin as an energy acceptor in these wide-band-capturing dyads was established. Efficiency of FRET evaluated from spectral overlap was found to be 95 and 98 % for the meso-linked and β-pyrrole-linked dyads, respectively. Furthermore, evidence for the occurrence of FRET from singlet-excited chlorin to bacteriochlorin was secured from studies involving femtosecond transient absorption studies in toluene. The measured FRET rate constants, kFRET, were in the order of 1011 s−1, suggesting the occurrence of ultrafast energy transfer in these dyads. Nanosecond transient absorption studies confirmed relaxation of the energy transfer product, 1BChl*, to its triplet state, 3Bchl*. The 3Bchl* thus generated was capable of producing singlet oxygen with quantum yields comparable to their monomeric entities. The occurrence of efficient FRET emitting in the far-red region and the ability to produce singlet oxygen make the present series of dyads useful for photonic, imaging and therapy applications. 相似文献
185.
Weiwei Liu Song Ou Xiang He Hongwen Hu Qiangjin Wu Zixiang Huang 《Journal of chemical crystallography》2003,33(10):795-798
1-Methyl-2-phenylindolizine-3-acetonitrile was unexpectedly obtained in the reaction of 1-methyl-2-phenylindolizine-3-thioaldehyde with cyanide ions. Its structure was determined by IR, 1H NMR, MS, elemental analyses, and X-ray crystallography. Colorless regular prism shaped crystals of C17H14N2 crystallize in the space group C2/c with cell dimensions a = 12.956(3) Å, b =10.516(2) Å, c = 20.429(4) Å, and = 90°, = 104.98(3)°, = 90°, V =2688.7(9) Å3, D
calc =1.217 Mg/m3, and Z = 8. 相似文献
186.
Guibin Yao Yuwei Fang Enyi Chi Jinbiao Bao Li Zhang Yiguo Li Jianqiang Zhang Zongbao Wang 《Polymer Science Series A》2018,60(5):663-670
Isotactic polypropylene (iPP)/reduced graphene oxide (RGO) nanocomposite bars were prepared by injection molding and the effects of RGO on the iPP matrix were investigated via differential scanning calorimetry, two dimensional wide angle X-ray diffraction (2D WAXD) and small angle X-ray scattering (2D SAXS) techniques. It is demonstrated that RGO is an effective nucleation agent for iPP and the incorporation of RGO can enhance the degree of orientation of iPP crystals at flow direction. Furthermore, the orientation of iPP chains at flow direction intensifies with the increase of RGO contents, which can be attributed to that RGO obstructed the motion of orientated polymer chains. Although the enhancement effect is weaker than that of High density polyethylene (HDPE)/RGO nanocomposites with epitaxial crystallization, the mechanical properties of iPP/RGO nanocomposites can also be improved apparently. 相似文献
187.
Electrochemical Reduction of Carbon Dioxide to Methanol on Hierarchical Pd/SnO2 Nanosheets with Abundant Pd–O–Sn Interfaces
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Wuyong Zhang Qing Qin Dr. Lei Dai Ruixuan Qin Dr. Xiaojing Zhao Xumao Chen Daohui Ou Dr. Jie Chen Dr. Tracy T Chuong Prof. Binghui Wu Prof. Nanfeng Zheng 《Angewandte Chemie (International ed. in English)》2018,57(30):9475-9479
Electrochemical conversion of CO2 into fuels using electricity generated from renewable sources helps to create an artificial carbon cycle. However, the low efficiency and poor stability hinder the practical use of most conventional electrocatalysts. In this work, a 2D hierarchical Pd/SnO2 structure, ultrathin Pd nanosheets partially capped by SnO2 nanoparticles, is designed to enable multi‐electron transfer for selective electroreduction of CO2 into CH3OH. Such a structure design not only enhances the adsorption of CO2 on SnO2, but also weakens the binding strength of CO on Pd due to the as‐built Pd–O–Sn interfaces, which is demonstrated to be critical to improve the electrocatalytic selectivity and stability of Pd catalysts. This work provides a new strategy to improve electrochemical performance of metal‐based catalysts by creating metal oxide interfaces for selective electroreduction of CO2. 相似文献
188.
Ming-Li Sun Feng Zhang Yan Qian Chang-Jin Ou Bin Liu Ling-Hai Xie Ying Wei Bao-Yi Ren Wei Huang 《Tetrahedron》2018,74(16):2063-2067
A green protocol with catalyst-free photo-induced cyclization for the synthesis of a spiro-fused organic semiconductor molecule based on spiro[fluorene-9,9′-xanthene] (SFX) was developed. The photophysical and electrochemical properties of the spiro-fused compound (DPCzSFX) have been characterized. The results showed that the molecular stability and the property of the charge injecting/transporting were improved due to the cyclization. And the broadening of the emission spectrum in film makes the sipro-fused compound possible for the application as a host in the white phosphorescent organic light-emitting diodes. However, the same reaction for the spirobifluorene-based dipenylamine derivative did not occur under the same condition, which also highlights the importance of the oxygen heteroatom in the ring to the reaction of cyclization. 相似文献
189.
Jianguang Lv Zhiqing He Jianmin Zhang Yuwei Guo Ziwei Han Xinhua Bao 《Tetrahedron》2018,74(29):3996-4004
A simple and efficient copper-catalyzed tandem radical cyclization reaction has been discovered for the synthesis of triaryl [1,2,4]triazolo[1,5-a]pyridines from easily accessible azines and benzylidenmalononitriles. The new transformation involves multiple CH/CC bonds cleavage and CC/CN bonds formation, with extrusion of gaseous hydrogen and methane. A wide variety of substrates with different functional groups could be converted into the corresponding products in good yields. The fused heterocycles have strong blue fluorescence with large Strokes shifts and high quantum yields. 相似文献
190.