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991.
Dokuburra Chanti BabuJondoss Jon Paul Selavam Dorigondla Kumar ReddyVanam Shekhar Yenamandra Venkateswarlu 《Tetrahedron》2011,67(21):3815-3819
A stereoselective total synthesis of (−)-cleistenolide (1) derived from d-(−)-isoascorbic acid has been described. The new synthetic strategy involves highly diastereoselective reduction, one-pot protection of required benzoyl, acetyl groups, and the RCM reaction by using Grubbs catalyst are the key steps with considerable yields. 相似文献
992.
Sudhir Kumar PandeyKi-Hyun Kim 《Trends in analytical chemistry : TRAC》2011,30(6):899-917
This review critically evaluates the measurement methodologies most commonly employed for the analysis of the various forms of mercury (Hg) in air. Emphasis is given to the three most common forms of mercury in air [i.e. gaseous elemental mercury (GEM, Hg0), reactive gaseous mercury (RGM), and particle-bound mercury (Hgp)]. Moreover, we also briefly describe methods dealing with gas-phase analysis of organic mercury species (e.g., mostly methyl mercury), as they are also reported to be present in air on rare occasions. To begin with, we describe the approaches to sampling airborne mercury species and associated sample-treatment strategies. We evaluate both conventional and emerging alternative detection techniques for different mercury forms with respect to their applicability in airborne mercury analysis. We also discuss the artifacts and the biases associated with analysis of different mercury species. Finally, the review summarizes current methodological developments for the determination of mercury in air and highlights future prospects for improvements. 相似文献
993.
Dipravath Kumar SethSamaresh Bhattacharya 《Polyhedron》2011,30(15):2438-2443
The reactions of N-(aryl)pyridine-2-aldimines (L-R; R = OCH3, CH3, H, Cl and NO2), derived from pyridine-2-aldehyde and para-substituted anilines, with CuI in methanol under ambient conditions afford a series of brown complexes of the type [{Cu(L-R)I}2]. The structure of the [{Cu(L-OCH3)I}2] complex has been determined by X-ray crystallography. In these dimeric complexes the two copper centers are linked through an iodo-bridge, and the L-R ligands are coordinated to the metal center through the pyridine-nitrogen and imine-nitrogen. All the complexes show characteristic 1H NMR signals and intense MLCT transitions in the visible region. These complexes also show an emission near 465 nm, whilst they are excited at 340 nm, with relatively poor quantum yields (φ ∼0.002 at 298 K). Cyclic voltammetry on all the complexes shows two successive Cu(I)-Cu(II) oxidations on the positive side of SCE, and a reduction of the coordinated imine ligand on the negative side. These copper(I) complexes are found to efficiently catalyze Suzuki type C-C coupling reactions. 相似文献
994.
The first examples of ring-closing metathesis (RCM) reactions of a series of terminal alkene-derived cyclic phosphazenes have been carried out. The tetrakis-, hexakis-, and octakis(allyloxy)cyclophosphazenes (NPPh(2))(NP(OCH(2)CH=CH(2))(2))(2) (1), N(3)P(3)(OCH(2)CH=CH(2))(6) (2), and N(4)P(4)(OCH(2)CH=CH(2))(8) (3) and the tetrakis(allyloxy)-S-phenylthionylphosphazene (NS(O)Ph)[NP(OCH(2)CH=CH(2))(2)](2) (4) were prepared by the reactions of CH(2)=CHCH(2)ONa with the cyclophosphazenes (NPPh(2))(NPCl(2))(2), N(3)P(3)Cl(6), and N(4)P(4)Cl(8) and the S-phenylthionylphosphazene (NS(O)Ph)(NPCl(2))(2). The reactions of 1-4 with Grubbs first-generation olefin metathesis catalyst Cl(2)Ru=CHPh(PCy(3))(2) resulted in the selective formation of seven-membered di-, tri-, and tetraspirocyclic phosphazene compounds (NPPh(2))[NP(OCH(2)CH=CHCH(2)O)](2) (5), N(3)P(3)(OCH(2)CH=CHCH(2)O)(3) (6), and N(4)P(4)(OCH(2)CH=CHCH(2)O)(4) (7) and the dispirocyclic S-phenylthionylphosphazene compound (NS(O)Ph)[NP(OCH(2)CH=CHCH(2)O)](2) (8). X-ray structural studies of 5-8 indicated that the double bond of the spiro-substituted cycloalkene units is in the cis orientation in these compounds. In contrast to the reactions of 1-4, RCM reactions of the homoallyloxy-derived cyclophosphazene and thionylphosphazene (NPPh(2))[NP(OCH(2)CH(2)CH=CH(2))(2)](2) (9) and (NS(O)Ph)[NP(OCH(2)CH(2)CH=CH(2))(2)](2) (10) with the same catalyst resulted in the formation of 11-membered diansa compounds NPPh(2)[NP(OCH(2)CH(2)CH=CHCH(2)CH(2)O)](2) (11) and (NS(O)Ph)[NP(OCH(2)CH(2)CH=CHCH(2)CH(2)O)](2) (13) and the intermolecular doubly bridged ansa-dibino-ansa compounds 12 and 14. The X-ray structural studies of compounds 11 and 13 indicated that the double bonds of the ansa-substituted cycloalkene units are in the trans orientation in these compounds. The geminal bis(homoallyloxy)tetraphenylcyclotriphosphazene [NPPh(2)](2)[NP(OCH(2)CH(2)CH=CH(2))(2)] (15) upon RCM with Grubbs first- and second-generation catalysts gave the spirocyclic product [NPPh(2)](2)[NP(OCH(2)CH(2)CH=CHCH(2)CH(2)O)] (16) along with the geminal dibino-substituted dimeric compound [NPPh(2)](2)[NP(OCH(2)CH(2)CH=CHCH(2)CH(2)O)(2)PN][NPPh(2)](2) (17) as the major product. The dibino compound 17, upon reaction with the Grubbs second-generation catalyst, was found to undergo a unique ring-opening metathesis reaction, opening up the bino bridges and partially converting to the spirocyclic compound 16. 相似文献
995.
Salaam Saleh Druthiman Reddy Mantheni Manik Pavan Kumar Maheswaram Susan Moreno-Molek Tobili Sam-Yellowe Alan T. Riga 《Journal of Thermal Analysis and Calorimetry》2013,111(3):1707-1716
Malaria affects over 500 million people worldwide leading to 1–2 million deaths each year, the majority of whom are children. Four Plasmodium species cause malaria in humans. To properly diagnose, and correctly treat malarial infections, accurate diagnosis of infection is required. Proper diagnosis of infection will result in a reduction of morbidity, mortality, and of drug resistant parasites. However, the current tests for malaria diagnosis do not efficiently identify the appropriate human and parasite biomarkers associated with disease. Detection of specific inflammatory mediators such as cytokines associated with malaria pathogenesis will aid the determination of disease progression, disease prognosis, and the early diagnosis of malaria infection. In this study, we used dielectric thermal analysis (DETA), thermogravimetric analysis, and differential scanning calorimetry (DSC) to characterize five human cytokines (IL-1α, IL-2, IL-4, IL-6, and IL-10), to demonstrate how their thermoanalytical properties can be investigated for sensor design. Analysis for DETA was performed at a frequency range of 0.1–300,000 Hz. Permittivity and loss factor measurements were used to calculate tan δ values. Peak frequencies were used to determine dielectric signatures for each cytokine. The peak frequencies were different for each cytokine analyzed. In addition, activation energies were frequency dependent for IL-2 but frequency independent for the remaining four cytokines. Cytokines were also examined using DSC which established variance in heat of crystallization and heat of fusion of solvent among the five cytokines. A noticeable differentiation was observed with IL-1α among the other four cytokines when analyzed using trend analysis. Detection of unique dielectric signals will aid development of sensitive dielectric sensors capable of detecting cytokines in various human samples. 相似文献
996.
Pandey R Kumar P Singh AK Shahid M Li PZ Singh SK Xu Q Misra A Pandey DS 《Inorganic chemistry》2011,50(8):3189-3197
Binuclear zinc(II) and copper(II) complexes based on a new Schiff base ligand N,N'-bis(2-hydroxybenzilidene)-2,4,6-trimethylbenzene-1,3-diamine (H(2)L) have been synthesized. The ligand H(2)L and complexes under investigation have been characterized by elemental analyses, spectral (FT-IR, (1)H, (13)C NMR, ESI-MS, electronic absorption, emission), and electrochemical studies. The structures of H(2)L and complexes [{Zn(C(23)H(18)N(2)O(2))}(2)] (1) and [{Cu(C(23)H(18)N(2)O(2))}(2)]·H(2)O (2) have been determined crystallographically. Selective "On-Off-On" switching behavior of the fluorescent complex 1 has been studied. The fluorescence intensity of 1 quenches (turns-off) upon addition of Cu(2+), while enhances (turns-on) in the presence of Ag(+) ions. The mechanisms of "On-Off-On" signaling have been supported by (1)H NMR, ESI-MS, electronic absorption, and emission spectral studies. Job's plot analysis supported 1:1 and 1:2 stoichiometries for Cu(2+) and Ag(+) ions, respectively. Association and quenching constants have been estimated by the Benesi-Hildebrand method and Stern-Volmer plot. Moreover, 1 mimics a molecular keypad lock that follows correct chemical input order to give maximum output signal. 相似文献
997.
Nazmul Abedin Khan Dinesh Kumar Mishra Jin-Soo Hwang Young-Woo Kwak Sung Hwa Jhung 《Research on Chemical Intermediates》2011,37(9):1231-1238
Liquid-phase dehydration of sorbitol has been investigated in wide reaction conditions especially under microwave irradiation in the presence of acidic resin catalysts. From the selectivity for sorbitan and isosorbide, it can be understood that the dehydration is a consecutive reaction (sorbitol to sorbitan, and finally to isosorbide) and that the sorbitan is an intermediate of the dehydration. By using microwave irradiation, the dehydration can be accelerated by around 20?C34 times compared with the rate by conventional electric heating at the same temperature, or the reaction temperature can be decreased by around 40 °C for the comparable conversion in a similar reaction time. However, the microwaves do not have noticeable effects on the selectivity for isosorbide or sorbitan. The accelerated dehydration under microwaves is mainly due to decreased activation energy. 相似文献
998.
Chemical Fixation of CO2 and Other Heterogeneous Catalytic Studies by Employing a Layered Cu‐Porphyrin Prepared Through Single‐Crystal to Single‐Crystal Exchange of a Zn Analogue 下载免费PDF全文
A solvothermal reaction of Zn(NO3)2 ? 6 H2O, tetra‐(4‐pyridyl)porphyrin (H2TPyP), and 4,4′‐oxybis(benzoic acid) (H2OBA) resulted in a new two‐dimensional Zn‐ porphyrin metal–organic framework compound, [Zn2(C40H24N8)0.5(C14H8O5)(DMA)](DMA)(H2O)6 ( 1 ; DMA=N,N‐dimethylacetamide). The ZnII ions present in 1 could be exchanged by using a solution of Cu(NO3)2 ? 3 H2O in DMA at room temperature to give [Cu2(C40H24N8)0.5(C14H8O5)(DMA)](DMA)(H2O)3 ( Cu∈1 ). The extra‐framework solvent molecules have been shown to be reversibly removed or exchanged without collapse of the framework. Solvent‐free Cu∈1 was explored as an active heterogeneous catalyst towards three different organic reactions: 1) the chemical fixation of CO2 into cyclic carbonate at room temperature and 1 atm; 2) the nitroaldol reaction under solvent‐free conditions, and 3) the three‐component coupling of aminopyridine, benzaldehyde, and aryl alkynes followed by 5‐exo‐dig cyclization to produce the important pharmacophore imidazopyridine. 相似文献
999.
Solvent‐Mediated Functionalization of Benzofuroxan on Electron‐Rich Ruthenium Complex Platform 下载免费PDF全文
Dr. Prabir Ghosh Sanchaita Dey Sanjib Panda Prof. Goutam Kumar Lahiri 《化学:亚洲杂志》2018,13(12):1582-1593
An unprecedented reactivity profile of biochemically relevant R‐benzofuroxan (R=H, Me, Cl), with high structural diversity and molecular complexity on a selective {Ru(acac)2} (acac=acetylacetonate) platform, in conjugation with EtOH solvent mediation, is revealed. This led to the development of monomeric [RuIII(acac)2(L1R)] ( 1 a – 1 c ; L1R=2‐nitrosoanilido derivatives) and dimeric [{RuII(acac)2}2(L2R)] ( 2 a – 2 b ; L2R=(1E,2E)‐N1,N2‐bis(2‐nitrosophenyl)ethane‐1,2‐diimine derivatives) complexes in one pot with a change in the metal redox conditions. The functionalization of benzofuroxan in 1 and 2 implied in situ reduction of N=O to NH? in the former and solvent‐assisted multiple N?C coupling in the latter. The aforesaid transformation processes were authenticated through structural elucidation of representative complexes, and evaluated by their spectroscopic/electrochemical features, along with C2D5OD labeling and monitoring of the impact of substituents (R) in the benzofuroxan framework on the product distribution process. The noninnocent potential of newly developed L1 and L2 in 1 and 2 , respectively, was also probed by spectroelectrochemistry in combination with DFT calculations. 相似文献
1000.
Deepika Kushwaha S. N. Upadhyay Pradeep Kumar Mishra 《Applied biochemistry and biotechnology》2018,184(4):1247-1262
Growths of Lyngbya limnetica and Oscillatoria obscura were investigated at varying pH, light intensity, temperature, and trace element concentration with a view to optimize these parameters for obtaining the maximum carbohydrate content. The maximum growth for both strains was obtained at pH 9.0 and temperature 20 ± 3 °C using a light intensity of 68.0 μmol m?2 s?1 with continuous shaking. Growth under the nitrogen starvation condition affected the carbohydrate content more compared to the phosphorus starvation, and maximum concentrations were found as 0.660 and 0.621 g/g of dry biomass for L. limnetica and O. obscura, respectively. Under the optimized nitrogen-rich conditions, the specific growth rates for the two strains were found to be 0.187 and 0.215 day?1, respectively. The two-stage growth studies under nitrogen-rich (stage I) followed by nitrogen starvation (stage II) conditions were performed, and maximum biomass and carbohydrate productivity were found as 0.088 and 0.423 g L?1 day?1 for L. limnetica. This is the first ever attempt to evaluate and optimize various parameters affecting the growth of cyanobacterial biomass of L. limnetica and O. obscura as well as their carbohydrate contents. 相似文献