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排序方式: 共有273条查询结果,搜索用时 31 毫秒
31.
This paper presents two deterministic inventory models for a single item, where for the first model, the production rate at any instant depends on the on-hand inventory and for the second one, it is demand dependent. However, in both cases, the demand rate at any moment of time is a linear function of time for the scheduling period. Both the models are formulated and solved without allowing shortages. Two numeric examples have been added to illustrate the results. 相似文献
32.
Prasenjit Mandal Rupali Kaul Tarun Jain 《European Journal of Operational Research》2018,264(1):181-199
In this paper, we study the newsvendor’s pricing and stocking decisions under reference point effects. The demand faced by the newsvendor is endogenous and the customers may also decide to procure the product from an outside option. We characterize the firm’s optimal pricing and stocking decisions. Our analysis reveals a threshold policy on the firm’s ordering and pricing decisions while considering the impact of reference point effects. We also find that as the level of optimism increases, the firm’s optimal ordering level decreases and optimal price increases. We further study the impact of loss aversion on the firm’s ordering and pricing decisions. 相似文献
33.
Ab initio theory at the HF/6-311G(d,p) level has been used to compute the hydrogen bonding thermodynamics in bulk liquid ethanol. Inter-cluster hydrogen bonding is assumed to mimic the H-bonding in bulk ethanol. Rotation of the clusters has been neglected, but translational and vibrational motions are taken into account for calculating bulk thermodynamic parameters. Results are well in agreement with an earlier report [J. Chem. Phys. 116, 4212 (2002)]. For a more accurate dipole moment of monomer, MP2/6-311++G(d,p) calculation was done. Use of the computed thermodynamic data in a statistical model yields the Kirkwood-Frohlich correlation factor and the dielectric constant of ethanol (21.0) close to the experimental value, 24.3 at 298 K. 相似文献
34.
Marcela R. Beltrán Fernando Buendía Zamudio Vikas Chauhan Prasenjit Sen Haopeng Wang Yeon Jae Ko Kit Bowen 《The European Physical Journal D - Atomic, Molecular, Optical and Plasma Physics》2013,67(3):1-8
We present an analysis of Na-He collisional profiles at high density and very low temperature in a unified line shape semi-classical theory which contains the impact as well the quasistatic limits. Clearly understanding the variation of shape of the two fine-structure components of the 3s?3p line with increasing helium density allows us to understand experimental spectra of a Na atom attached to He nanodroplets. We compare our collisional approach to path integral Monte Carlo calculations using the same ab initio Na-He molecular potentials. 相似文献
35.
Molecular Diversity - In this study, an efficient and convenient domino Michael addition/intramolecular cyclization protocol is presented for the synthesis of biologically relevant... 相似文献
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Prasenjit Das Jérôme Roeser Arne Thomas 《Angewandte Chemie (International ed. in English)》2023,62(29):e202304349
A chemically stable 2D microporous COF ( PMCR-1 ) was synthesized via the multicomponent Povarov reaction. PMCR-1 exhibits a remarkable and long-term stable photocatalytic H2O2 production rate (60 h) from pure and sea water under visible light. The H2O2 production is markedly enhanced when benzyl alcohol (BA) is added as reductant, which is also due to a strong π–π interaction of BA with dangling phenyl moieties in the COF pores introduced by the multicomponent Povarov reaction. Motivated by the concomitant BA oxidation to benzaldehyde during H2O2 formation, the photocatalytic oxidation of various organic substrates such as benzyl amine and methyl sulfide derivatives was investigated. It is shown that the well-defined micropores of PMCR-1 enable size-selective photocatalytic oxidation. 相似文献
39.
[Ni(NaiR)2(X)2] (X = N3 (3, 4) and NCS (5, 6) complexes are synthesized from the reaction of Ni(ClO4)2 · 6H2O with 1-alkyl-2-(naphthyl-α/β-azo)imidazole (α/β-NaiR) and sodium azide (NaN3) or ammonium thiocyanate (NH4NCS) (1:2:2 molar ratio) in methanol solution. The complexes are characterized by elemental, spectroscopic and magnetic study. The distorted octahedral structure has been confirmed by single crystal X-ray diffraction study of [Ni(β-NaiEt)2(NCS)2] (6b). Cyclic voltammogram exhibits quasireversible oxidation response at 0.3–0.4 V which is corresponding to Ni(III)/Ni(II) couple along with ligand reductions at negative potential to SCE reference electrode. 相似文献
40.
A series of structurally diverse gold and silver complexes extending from ionic (NHC) 2M(+)Cl(-) (M=Au, Ag) type complexes to large 12-membered macrometallacycles have been prepared by the appropriate modification of the N-substituent of amido-functionalized N-heterocyclic carbenes. Specifically, the ionic, [1-(R)-3-{ N-(t-butylacetamido)imidazol-2-ylidene}]2M(+)Cl(-), (R=t-Bu, i-Pr; M=Au, Ag; 1b, 1c, 2b, 2c) complexes, were obtained in case of the N- t-butyl substituent of the amido-functionalized sidearm while 12-membered macrometallacycles, [1-(R)-3-{N-(2,6-di i-propylphenylacetamido)imidazol-2-ylidene}]2M2, (R=t-Bu, i-Pr; M=Au, Ag; 3b, 3c, 4b, 4c) were obtained in case of the 2,6-di i-propylphenyl N-substituent. These structurally diverse complexes of gold and silver were, however, prepared employing a common synthetic pathway involving the reactions of the imidazolium chloride salts (1a, 2a, 3a, 4a) with Ag2O to give the silver complexes (1b, 2b, 3b, 4b) and which, when treated with (SMe2)AuCl, gave the gold complexes (1c, 2c, 3c, 4c). Detailed density functional theory studies of 1b, 1c, 2b, 2c, 3b, 3c, 4b, and 4c were carried out to gain insight about the structure, bonding, and the electronic properties of these complexes. The NHC-metal interaction in the ionic 1b, 1c, 2b, and 2c complexes is primarily composed of the interaction of the carbene lone pair with the empty p orbital of the metal (5p for Ag and 6p for Au) while the same in the macrometallacyclic 3b, 3c, 4b, and 4c complexes consisted of the interaction of the carbene lone pair with the empty s orbital of the metal (5s for Ag and 6s for Au). The observation of a low energy emission in about the 580-650 nm region has been tentatively assigned to originate from the presence of weak metallophilic interaction in these macrometallacyclic 3b, 3c, 4b, and 4c complexes. 相似文献