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排序方式: 共有1103条查询结果,搜索用时 46 毫秒
31.
Renu Sharma Santosh K. Agarwal Shikha Rawat Meena Nagar 《Transition Metal Chemistry》2006,31(2):201-206
The synthesis and characterization of some transition metal cis-3,7-dimethyl-2,6-octadiensemicarbazone (CDOSC) complexes are reported. The ligand CDOSC yields: [ML2 Cl2] and [ML2 Cl2] Cl type complexes, where M = CrIII, MnII, FeIII, CoII, NiII, CuII, ZnII, CdII and HgII, L = CDOSC. Structures of the complexes were determined using elemental analysis, molar conductivity, magnetic measurements,
i.r. and electronic, as well as n.m.r spectra. CDOSC acts as a bidentate ligand in all the complexes. All the newly synthesized
metal complexes, as well as the ligand, were screened for their antibacterial activity. All the complexes exhibit strong inhibitory
action against Gram (+) bacteria Staphylococcus aureus and Gram (−) bacteria Escherichia coli. The antibacterial activities of the complexes are stronger than those of the ligand CDOSC itself. 相似文献
32.
Santosh K. Mondal Parimal Paul Rita Roy Kamalaksha Nag 《Transition Metal Chemistry》1984,9(7):247-250
Summary Complexes of nickel(II), palladium(II), copper(II), cobalt(II), and cobalt(III) with methyl-2-(-salicylaldiminoethyl)-cyclopent-1-en-dithiocarboxylate (H2L1) and methyl-2-(-salicylaldiminoisopropyl)cyclopent-1-en-dithiocarboxylate (H2L2) have been prepared. They contain the donor sites ONNS. The metal(II) ions from neutral, monomeric square planar chelate complexes. The cobalt(III) complexes [CoL1-(H2O)2]X (X=Cl or ClO4) appear to betrans-diaqua-species. All compounds have been characterized by a number of physico-chemical methods. 相似文献
33.
Partha Sarathi Das Basudam Adhikari Sukumar Maiti 《Journal of polymer science. Part A, Polymer chemistry》1994,32(1):39-45
Fluorination of low-density polyethylene, polyacetylene, and poly(vinyl alcohol) was carried out using SF6 gas under electric discharge. The polymers were partially fluorinated and the extent of fluorination was more in the case of poly (vinyl alcohol) than the other two polymers. The fluorinated polymers were characterized by elemental analysis (Fluorine), IR, and x-ray diffraction. Optical transparency of the films was also measured. The fluorinated polymers show better solvent resistance and decreased transparency than the virgin polymer. © 1994 John Wiley & Sons, Inc. 相似文献
34.
Summary The kinetics of oxidation of aldoses, namely xylose, arabinose, galactose and glucose, by CeIV have been studied in HClO4 + H2SO4 medium and in the presence of PdII. The reactions exhibit a first order rate dependence with respect to oxidant. The rate is inversely dependent on the [HSO
inf4
sup–
][H+] ratio. The order of reaction with respect to aldose decreases at higher [aldose]. Due to the formation of a complex between CeIV and PdII, a retarding effect of [PdII] on the rate of disappearance of [CeIV] has been observed. A mechanism consistent with the observed kinetic data is proposed. 相似文献
35.
Kumar S Rai AK Singh VB Rai SB 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2005,61(11-12):2741-2746
The infrared and Raman spectra of glycine molecule has been studied in spectral region 400-4000 cm(-1) in solid form as well as in water. The vibrational frequencies for the fundamental modes of the glycine in neutral and its zwitterionic form have also been calculated using AM1 semiempirical method as well as ab initio method with minimal basis set. The reliability of the minimal basis set and AM1 method with higher basis sets, for IR spectra of the neutral glycine conformers were examined. We find that the 6-21G basis set calculation yields structural parameters, rotational constant and dipole moment of glycine conformers, which are very similar to those obtained from extended basis set calculation as well as experimental values. IR frequencies for glycine conformer I are also calculated in water using SCRF=PCM model and compared with experimental values. A comparison between calculated frequencies for neutral glycine, and its zwitterionic form with observed IR and Raman bands have been made. The total energies for gas phase glycine and its zwitterionic form along with those of hydrated forms were also calculated. It is found from the calculations that in the gas phase neutral glycine is more stable as compared to its zwitterionic form. 相似文献
36.
In the present study, the recyclability of the post-use milk pouches (50/50 LDPE–LLDPE blend) was evaluated with or without adding stabilizer. Thoroughly washed and dried post-use milk pouch films were extruded five times at high temperature (483–513 K) in the open atmosphere. The mode of degradation during extrusion operation was studied by melt flow index (MFI), rheological properties, gel content and FT-IR analysis. The differential scanning calorimetry (DSC) analysis was carried out to evaluate the thermal stability of the stabilized and un-stabilized recycled mass from post-use milk pouch under this investigation. Mechanical properties (tensile strength, % elongation at break, tensile modulus and hardness) of the un-stabilized extruded material were significantly affected as a result of thermooxidative degradation during extrusion in presence of air. After all, stabilization with 0.4% anti-oxidant satisfactorily retains all the initial properties of the recycled material. 相似文献
37.
Anil K. Awasthi Santosh K. Upadhyay 《Monatshefte für Chemie / Chemical Monthly》1985,116(6-7):729-736
The kinetics of ruthenium(III) catalyzed oxidation of formaldehyde and acetaldehyde by alkaline hexacyanoferrate(III) has been studied spectrophotometrically. The rate of oxidation of formaldehyde is directly proportional to [Fe(CN)
3–
6
] while that of acetaldehyde is proportional tok[Fe(CN)
3–
6
]/{k +k[Fe(CN)
3–
6
]}, wherek, k andk are rate constants. The order of reaction in acetylaldehyde is unity while that in formaldehyde falls from 1 to 0. The rate of reaction is proportional to [Ru(III)]
T
in each case. A suitable mechanism is proposed and discussed.
Die Kinetik der Ru(III)-katalysierten Oxidation von Formaldehyd und Acetaldehyd mittels alkalischem Hexacyanoferrat(III)
Zusammenfassung Die Untersuchung der Kinetik erfolgte spektrophotometrisch. Die Geschwindigkeitskonstante der Oxidation von Formaldehyd ist direkt proportional zu [Fe(CN) 3– 6 ], währenddessen die entsprechende Konstante für Acetaldehyd proportional zuk[Fe(CN) 3– 6 ]/{k +k[Fe(CN) 3– 6 ]} ist, wobeik,k undk Geschwindigkeitskonstanten sind. Die Reaktionsordnung für Acetaldehyd ist eine erste, die für Formaldehyd fällt von erster bis zu nullter Ordnung. Die Geschwindigkeitskonstante ist in jedem Fall proportional zu [Ru(III)] T . Es wird ein passender Mechanismus vorgeschlagen.相似文献
38.
39.
Biranje Santosh Shivaji Sun Jianzhong Shi Yifei Yu Sujie Jiao Haixin Zhang Meng Wang Qianqian Wang Jin Liu Jun 《Cellulose (London, England)》2021,28(14):8899-8937
Cellulose - Excessive hemorrhage is a leading cause of death to trauma patients, especially in combat and civilian accidents. The main priority in the medical treatment of trauma patients is to... 相似文献
40.
Ranjit Joshi Jörg Friedrich Santosh Krishna-Subramanian 《Plasma Chemistry and Plasma Processing》2013,33(5):921-940
Ultra-high molecular weight polyethylene membranes were modified and subsequently polymer coated using the underwater plasma produced by glow discharge electrolysis. This plasma pretreatment generated various O-functional groups among them OH groups have dominated. This modified inner (pore) surface of membranes showed complete wetting and strong adhesion to a hydrogel copolymerized by glow discharge electrolysis also. The deposited hydrogel consists of plasma polymerized acrylic acid crosslinked by copolymerization with the bifunctional N,N′-methylenebis(acrylamide). Tuning the hydrogel hydrophilicity and bio-compatibility poly(ethylene glycol) was chemically inserted into the copolymer. Such saturated polymer could only be inserted on a non-classic way by (partial) fragmentation and recombination thus demonstrating the exotic properties of the underwater plasma. The modification of membrane was achieved by squeezing the reactive plasma solution into the pores by plasma-induced shock waves and supported by intense stirring. The deposited copolymer hydrogel has filled all pores also in the inner of membrane as shown by scanning electron microscopy of cross-sections. The copolymer shows the characteristic units of acrylic acid and ethylene glycol as demonstrated by infrared spectroscopy. A minimum loss in carboxylic groups of acrylic acid during the plasma polymerization process was confirmed by X-ray photoelectron spectroscopy. Additional cell adhesion tests on copolymer coated polyethylene using IEC-6 cells demonstrated the bio-compatibility of the plasma-deposited hydrogel. 相似文献