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排序方式: 共有194条查询结果,搜索用时 15 毫秒
1.
Thyagarajan S Shay DT Incarvito CD Rheingold AL Theopold KH 《Journal of the American Chemical Society》2003,125(15):4440-4441
Reaction of TpR,MeCo(I) dinitrogen complexes (R = iPr, tBu) with trimethylsilyl azide yields structurally characterized compounds that imply the formation of reactive intermediates of the type TpR,MeCo=NSiMe3. These cobalt imido species apparently abstract hydrogen from the 3-substituent of the Tp-ligand, leading to the formation of amido complexes accompanied by either Co-C bond formation (R = tBu) or C-C bond formation (R = iPr). 相似文献
2.
Reaction of cis-[PtCl2(AsPh3)2] with excess sodium sulfide in benzene gave the triphenylarsine analogue of the well-known metalloligand [Pt2(μ-S)2(PPh3)4] as an orange solid.The compound was characterised by detailed mass spectrometry studies, and by conversion to various alkylated and metallated derivatives.The sulfide ligands in [Pt2(μ-S)2(AsPh3)4] are less basic than the triphenylphosphine analogue, and the complex gives a relatively weak [M+H]+ ion in the positive-ion electrospray (ESI) mass spectrum, compared with the phosphine analogue.Methylation of an equimolar mixture of [Pt2(μ-S)2(PPh3)4] and [Pt2(μ-S)2(AsPh3)4] with MeI gave the species [Pt2(μ-S)(μ-SMe)(AsPh3)4]+ and [Pt2(μ-SMe)2(PPh3)3I]+, indicating a reduced tendency for the sulfide of [Pt2(μ-S)(μ-SMe)(AsPh3)4]+ to undergo alkylation.The lability of the arsine ligands is confirmed by the reaction of an equimolar mixture of [Pt2(μ-S)2(PPh3)4] and [Pt2(μ-S)2(AsPh3)4] with n-butyl chloride, giving [Pt2(μ-S)(μ-SBu)(EPh3)4]+ (E = P, As), which with Me2SO4 gave a mixture of [Pt2(μ-SMe)(μ-SBu)(PPh3)4]2+ and [Pt2(μ-SMe)(μ-SBu)(AsPh3)3Cl]+.Reactivity towards 1,2-dichloroethane follows a similar pattern.The formation and ESI MS detection of mixed phosphine-arsine {Pt2S2} species of the type[Pt2(μ-S)2(AsPh3)n(PPh3)4−n] is also discussed. Coordination chemistry of [Pt2(μ-S)2(AsPh3)4] towards a range of metal-chloride substrates, forming sulfide-bridged trinuclear aggregates, has also been probed using ESI MS, and found to be similar to the phosphine analogue. The X-ray crystal structure of [Pt2(μ-S)2(AsPh3)4Pt(cod)](PF6)2 (cod = 1,5-cyclo-octadiene) has been determined for comparison with the (previously reported) triphenylphosphine analogue. ESI MS is a powerful tool in exploring the chemistry of this system; in some cases the derivatising agent p-bromobenzyl bromide is used to convert sparingly soluble and/or poorly ionising {Pt2S2} species into soluble, charged derivatives for MS analysis. 相似文献
3.
Karishna C. Joshi Anshu Dandia Sunita Baweja Amitabh Joshi 《Journal of heterocyclic chemistry》1989,26(4):1097-1099
An elegant one-step synthesis of two novel spiro ring systems viz: spiro[3H-indole-3,4′-(2′-amino-3′-carbonitrile-[4′H]-pyrano[3,2-c]benzopyran)]-2,5′(1H)-dione8 and spiro[(2-amino-3-carbonitrile-indeno[1,2-b]pyran)-4(5H)>3′-[3H]indole]-2′,5(1′H)-diones in 80–85% yields is described. The spiro heterocycles were prepared by the reactions of fluorine containing 3-dicyanomethylene-2H-indol-2-ones with 4-hydroxy-2H-1-benzopyran-2-one and 1H-indene-1,3(2H)-dione respectively. The synthesized compounds have been characterized on the basis of elemental analyses, ir, pmr, 19F nmr and mass spectral data. 相似文献
4.
Ln0.5A0.5MnO3 (Ln=Lanthanide,A= Ca,Sr) Perovskites Exhibiting Remarkable Performance in the Thermochemical Generation of CO and H2 from CO2 and H2O
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Sunita Dey Dr. B. S. Naidu Prof. C. N. R. Rao 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(19):7077-7081
Perovskite oxides of the Ln0.5A0.5MnO3 (Ln=lanthanide, A=Sr, Ca) family have been investigated for the thermochemical splitting of H2O and CO2 to produce H2 and CO respectively. The amounts of O2 and CO produced strongly depend on the size of the rare earth ions and alkaline earth ions. The manganite with the smallest rare earth possessing the highest distortion and size disorder as well as the smallest tolerance factor, gives out the maximum amount of O2, and, hence, the maximum amount of CO. Thus, the best results are found with Y0.5Sr0.5MnO3, which possesses the highest distortion and size disorder. Y0.5Sr0.5MnO3 shows remarkable fuel production activity even at the reduction and oxidation temperatures as low as 1200 °C and 900 °C, respectively. 相似文献
5.
Subhash C. Jain Pankaj Khanna Sunita Bhagat Manish Jain Rajeev Sakhuja 《Phosphorus, sulfur, and silicon and the related elements》2013,188(8):1829-1839
The reaction of indol-2,3-diones ( 1a–i ) with 5-aminoindazole ( 2 ) has resulted in the formation of hitherto unknown 3-(indazol-5-yl)iminoindol-2-ones ( 3a–i ) in quantitative yields which, on 1,3-dipolar cyclocondensation with mercaptoacetic acid ( 4 ), has afforded a series of new spiro heterocycles, 3′-(indazol-5-yl) spiro[3H, indol-3, 2′ -thiazolidine]-2,4′-diones* ( 5a–i ). 相似文献
6.
The reaction of 1H‐indol‐2,3‐diones with 1,6‐dibromohexane has resulted in the formation of new 1H‐indol‐2,3‐diones‐1,1′‐(1,6‐hexanediyl)bis in quantitative yields. These compounds have been used for the synthesis of novel [3′‐(2,3‐dimethyl‐5‐oxo‐1‐phenyl‐3‐pyrazolin‐4‐yl)spiro[3H‐indol‐3,2′‐thiazolidine]‐2,4′‐dione]‐1,1′‐(1,6‐hexanediyl)bis via bis Schiff's bases, [3‐(2,3‐dimethyl‐5‐oxo‐1‐phenyl‐3‐pyrazolin‐4‐yl) imino‐1H‐indol‐2‐one]‐1,1′‐(1,6‐hexanediyl)bis. 相似文献
7.
Kallol K. Ghosh Sunita Bal Manmohan L. Satnami P. Rodriguez‐Dafonte Rama M. Palepu 《Journal of Dispersion Science and Technology》2013,34(3):349-355
Pseudo‐first‐order rate constants have been determined for the nucleophilic substitution reactions of p‐nitrophenyl acetate with oxalo, malono, and succinodihydroxamate ions (?ONHC(O)(CH2)nC(O)NHO?) in phosphate buffer (pH=7.9) at 27°C. The rate data of the reaction revealed that the nucleophilic reactivity sequence of these hydroxamate ions is generally ODHA>MDHA>SDHA. The kobs value increases upon addition of cationic surfactants to the reaction medium which is typical behavior of micelle‐assisted bimolecular reactions. The pseudo‐phase ion exchange model has been successfully applied to determine binding constant. 相似文献
8.
9.
K. D. Mandal Laxman Singh Sunita Sharma U. S. Rai M. M. Singh 《Journal of Sol-Gel Science and Technology》2013,66(1):50-58
Effect of doping at Ti4+ site by Ce3+ has been examined in CaCu3Ti3.90Ce0.10O12 synthesized by citrate-gel route. DTA/TG analysis of dry powder gives pre-information about formation of final product around 850 °C. X ray diffraction analysis confirmed the formation of CaCu3Ti3.90Ce0.10O12 phase of the ceramic sintered at 950 °C for 12 h. Microstructure has been studied using scanning electron microscopy and confirmed the average grain size found in nano range 200–400 nm in system CaCu3Ti3.90Ce0.10O12.The nature of relaxation behavior of ceramic was also rationalized by using the impedance and modulus spectroscopy. The bulk conductivity indicates an Arrhenius-type thermally activated process. The ac conductivity spectrum obeyed the Jonscher power law. The complex impedance diagrams of the ceramic exhibited a significant contribution from the grains, grain boundaries and electrode. The activation energies calculated from the grain-boundary relaxation time constant was found to be 0.49 eV which confirmed the Maxwell–Wagner type of relaxation present in the ceramic. 相似文献
10.
Aradhya Dev Srivastav Vireshwar Singh Deepak Singh Sunita Singh Suresh Kumar Patel Dilip Kumar Sudeep Yadav Balendu Shekher Giri Dhananjay Singh 《印度化学会志》2022,99(8):100632
Nelumbo nucifera leaves are rich source of natural wax possessing super-hydrophobic properties. It provides protection to them from ecological turbulences and climatic wear and tear. In this study, various experiments have been conducted to observe the yield of extraction and the determination of various functional groups, which are present in natural wax, derived from Nelumbo nucifera leaves. The natural wax has been extracted from lotus leaves through non-polar (hexane) and polar (ethanol) solvent via different extraction methods. The superhydrophobic wax has been successfully extracted with hexane. Whereas, ethanol did not extract the water-repellent wax of lotus leaf. Considering the cumulative amount, i.e. (desired + undesired), the maceration shows the extraction of 2.9% (%w/w, through hexane) and 10.2% (%w/w, through ethanol), while it was found 2.5% (%w/w, cycle period 15 min) and 9.0% (%w/w, cycle period 26 min) respectively, in case of Soxhlet extraction technique. For this specific case of natural wax recovery from biomass (lotus leaf), the maceration (traditional method) resulted a little bit superior extraction yield in comparison to the Soxhlet extraction method for extraction of crude wax. In the case of non-polar solvent (hexane), an extraction yield of 1.97% (%w/w) through maceration method was observed while in the case of non-polar solvent (ethanol), an extraction yield of 1.62% (%w/w) through Soxhlet extraction was observed. The TLC analysis on both types of extracts was performed. For the detection of various hydrocarbon chains in the crude wax extracts, FTIR was also performed. Topography of wax surface and wax-coated waterproof fabric was compared through SEM. 相似文献