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排序方式: 共有1170条查询结果,搜索用时 15 毫秒
91.
Manirul Islam Paramita Mondal Anupam Singha Roy Kazi Tuhina 《Transition Metal Chemistry》2010,35(4):427-435
A poly(3,6-dibenzaldimino N-vinyl carbazole) Pd(II) complex has been synthesized and characterized by physicochemical and spectroscopic techniques. The complex was found to be highly active toward hydrogenation reactions of various organic substrates under atmospheric pressure at ambient temperature. A tentative reaction mechanism is proposed on the basis of kinetic studies and isolation of reactive intermediates. The catalyst shows good conversion rates, thermal stability and recyclability. 相似文献
92.
Asim K. Das Sudhin K. Mondal Goutam Mukherjee 《Reaction Kinetics and Catalysis Letters》2001,73(2):257-265
Cetylpyridinium chloride (CPC) inhibits the Cr(VI) oxidation of ethanol and propan-1-ol while sodium dodecyl sulfate (SDS)
catalyzes the title reactions. At higher values of the [surfactant], the rate attains a limiting value. The micellar effect
has been explained by considering the preferential partitioning of the reactants in terms of the suggested mechanism. Applicability
of the Menger-Portnoy model and Piszkiewicz model to explain the observed micellar effect has been examined.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
93.
We define equivariant cyclic and Hochschild cohomology modules of a cyclic objectX in the category ofG-sets and relate them with the Bredon cohomologies of the cyclic geometric realization |X|cy. 相似文献
94.
Sodium Formate‐Catalyzed One‐Pot Synthesis of Benzopyranopyrimidines and 4‐Thio‐substituted 4H‐Chromenes via Multicomponent Reaction at Room Temperature 下载免费PDF全文
A simple, straightforward and highly efficient multicomponent one‐pot synthesis of a series of pharmaceutically interesting benzopyranopyrimidine and 4H‐chromene derivatives has been developed on the basis of low‐cost and environment‐friendly sodium formate catalyst via tandem reactions of salicylic aldehydes, malononitrile, and cyclic secondary amines in ethanol at room temperature. Nature of nucleophile used in this reaction directs the course of the reaction; cyclic secondary amines result in the formation of benzopyrano[2,3‐d]pyrimidines, whereas thiophenol furnish corresponding 4‐thio‐subtituted 4H‐chromenes under the same reaction conditions. High atom‐economy, good yields, eco‐friendly, and mild reaction conditions are some of the important features of this protocol. 相似文献
95.
Two CdII/CoII‐Imidazolate Coordination Polymers: Syntheses,Crystal Structures,Stabilities, and Luminescent/Magnetic Properties 下载免费PDF全文
Suvendu Sekhar Mondal Karsten Behrens Alexandra Kelling Hans‐Peter Nabein Uwe Schilde Hans‐Jürgen Holdt 《无机化学与普通化学杂志》2015,641(11):1991-1997
Cadmium(II) based 2D coordination polymer [Cd(L1)2(DMF)2] ( 1 ) (L1 = 4,5‐dicyano‐2‐methylimidazolate, DMF = N,N′‐dimethylformamide) and 2D cobalt(II)‐imidazolate framework [Co(L3)4] ( 2 ) (L3 = 4,5‐diamide‐2‐ethoxyimidazolate) were synthesized under solvothermal reaction conditions. The materials were characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis, powder X‐ray diffraction measurement (PXRD) and single‐crystal X‐ray diffraction. Compound 1 has hexacoordinate CdII ions and forms a zigzag chain‐like coordination polymer structure, whereas compound 2 exhibits a 2D square grid type structure. The thermal stability analysis reveals that 2 showed an exceptional thermal stability up to 360 °C. Also, 2 maintained its fully crystalline integrity in boiling water as confirmed by PXRD. The solid state luminescent property of 1 was not observed at room temperature. Compound 2 showed an independent high spin central CoII atom. 相似文献
96.
Effect of microhydration on the atmospherically important metastable carbonyl sulfide anion: Structure,energetic, and infrared study 下载免费PDF全文
Saptarsi Mondal Avula Uday Teja Prashant Chandra Singh 《International journal of quantum chemistry》2015,115(12):785-795
Structure, energetics, and vibrational frequency of the microhydrated carbonyl sulfide anion [OCS?? (H2O)n (n = 1–6)] have been explored by the systematic ab initio study to have a comprehensive understanding about the hydration‐induced stabilization phenomenon of OCS?. Water binds with the OCS? in single hydrogen‐bonded (SHB) or double hydrogen‐bonded (DHB) fashion with O? H S and O? H O contacts. Maximum five water molecules can stay in a cyclic water network of these hydrated clusters forming interwater hydrogen bonding (IHB) with each other and out of this, maximum of two water molecules can bind directly to the OCS? in (DHB) arrangement. The stabilization energy values of OCS?? (H2O)n depict that ion–water interaction is significant up to four water molecules and beyond that OCS? is stabilized by IHB between the water molecules. The CO stretching frequency of OCS? gets red shifted, whereas CS stretching frequency gets blue shifted on hydration. Charge analysis of hydrated clusters of OCS? indicates that negative charge moves toward oxygen from sulfur on hydration. © 2015 Wiley Periodicals, Inc. 相似文献
97.
Sanchita Mondal Saikat Kumar Manna Kalipada Maiti Rajkishor Maji Syed Samim Ali Srimanta Manna 《Supramolecular chemistry》2017,29(8):616-626
A FRET-based chemosensor L containing donor phenanthroline and acceptor fluorescein moiety was designed, synthesised and characterised for the ratiometric fluorescent detection of Cu2+ in organo-aqueous solution. Probe L showed high selectivity and excellent sensitivity towards Cu2+ ions by exhibiting both colorimetric and fluorometric changes due to opening of the spirolactum ring of fluorescein upon complexation with Cu2+. In presence of Cu2+ ions, probe L formed L-Cu2+ complex in 1:1 stoichiometric fashion which is established on the basis of Job’s plot and mass spectroscopy. We also performed DFT computational studies to know the binding nature and coordination feature of the complex. Furthermore, fluorescence imaging studies revealed that probe L was cell permeable and could be used to detect intracellular Cu2+ in living cells. 相似文献
98.
Goutam Dutta Krishnendranath Mitra 《The Journal of the Operational Research Society》2017,68(10):1131-1145
Revenue management and dynamic pricing are concepts that have immense possibilities for application in the energy sector. Both can be considered as demand-side management tools that can facilitate the offering of different prices at different demand levels. This paper studies literature on various topics related to the dynamic pricing of electricity and lists future research avenues in pricing policies, consumers’ willingness to pay and market segmentation in this field. Demand and price forecasting play an important role in determining prices and scheduling load in dynamic pricing environments. This allows different forms of dynamic pricing policies to different markets and customers depending on customers’ willingness to pay. Consumers’ willingness to pay for electricity services is also necessary in setting price limits depending on the demand and demand response curve. Market segmentation can enhance the effects of such pricing schemes. Appropriate scheduling of electrical load enhances the consumer response to dynamic tariffs. 相似文献
99.
Arindam MaityShyamal Mondal Rupankar PairaAbhijit Hazra Subhendu NaskarKrishnendu B. Sahu Pritam SahaSukdeb Banerjee Nirup B. Mondal 《Tetrahedron letters》2011,52(23):3033-3037
A convenient and inexpensive one step methodology has been developed for the synthesis of linear and angular fused quinazolinones. The protocol, which uses amino heterocycles and o-bromo benzyl/naphthyl bromides as reactants, CuI as catalyst, Cs2CO3 as base, l-proline as ligand, and DMF as solvent, proceeds via nucleophilic aromatic substitution of the N-heteroaromatic cationic intermediate followed by in situ aerial oxidation at the benzylic position to the quinazolinone scaffold. 相似文献
100.
Manirul?IslamEmail author Dildar?Hossain Paramita?Mondal Kazi?Tuhina Anupam?Singha?Roy Sanchita?Mondal Manir?Mobarak 《Transition Metal Chemistry》2011,36(2):223-230
A thiosemicarbazone Cu(II) complex anchored to a polystyrene framework has been synthesized and characterized by analytical
and spectroscopic techniques. The complex was found to be a highly active catalyst for the oxidation of various organic substrates
including alkenes and alcohols using H2O2 as oxidant. The reaction conditions were optimized with respect to temperature, solvent, oxidant, catalyst amount, and substrate
to peroxide ratio. The heterogeneous catalyst was reused five times without significant loss of activity. A comparison between
the catalytic activities of this polymer-supported Cu(II) complex and its homogeneous analogue was carried out. 相似文献