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51.
Shazia Iqbal Maria A. Khan Zulqarnain Ansari Almas Jabeen Aisha Faheem Saba Fazal-Ur-Rehman 《合成通讯》2013,43(18):2330-2341
AbstractCarbazole analogs 3 and 4 and a new library of bicarbazole-linked triazoles 6–11 were prepared via new synthetic methodology. Metal-catalyzed oxidative coupling reaction was utilized for the synthesis of bicarbazole acetylene 4 and different metals (Zn+2, Co+2, Fe+3, Ni+2, Cu+2, Mn+2) as catalyst were screened. Only Fe-catalyzed reaction was found to be excellent and gave homocoupled product 4. Cu-catalyzed 1,3-dipolar cycloaddition was also utilized to install triazole moiety for the synthesis of hybrid molecules 6–11. Based on reported anti-inflammatory activity of carbazole and triazole scaffolds, all compounds were screened for their reactive oxygen species (ROS) inhibitory potential. Results from these studies revealed triazole 9 as most active compound (IC50 value of 7.6?±?0.1?µg/mL on human whole blood and 2.7?±?0.09?µg/mL on isolated neutrophils) using ibuprofen as a standard. Therefore, class described herein can serve as attractive structural element for further studies on ROS inhibition. 相似文献
52.
This article deals with the hitherto unexplored metal complexes of deprotonated 6,12‐di(pyridin‐2‐yl)‐5,11‐dihydroindolo[3,2‐b]carbazole (H2L). The synthesis and structural, optical, electrochemical characterization of dimeric [{RuIII(acac)2}2(μ‐L.?)]ClO4 ([ 1 ]ClO4, S=1/2), [{RuII(bpy)2}2(μ‐L.?)](ClO4)3 ([ 2 ](ClO4)3, S=1/2), [{RuII(pap)2}2(μ‐L2?)](ClO4)2 ([ 4 ](ClO4)2, S=0), and monomeric [(bpy)2RuII(HL?)]ClO4 ([ 3 ]ClO4, S=0), [(pap)2RuII(HL?)]ClO4 ([ 5 ]ClO4, S=0) (acac=σ‐donating acetylacetonate, bpy=moderately π‐accepting 2,2’‐bipyridine, pap=strongly π‐accepting 2‐phenylazopyridine) are reported. The radical and dianionic states of deprotonated L in isolated dimeric 1 +/ 2 3+ and 4 2+, respectively, could be attributed to the varying electronic features of the ancillary (acac, bpy, and pap) ligands, as was reflected in their redox potentials. Perturbation of the energy level of the deprotonated L or HL upon coordination with {Ru(acac)2}, {Ru(bpy)2}, or {Ru(pap)2} led to the smaller energy gap in the frontier molecular orbitals (FMO), resulting in bathochromically shifted NIR absorption bands (800–2000 nm) in the accessible redox states of the complexes, which varied to some extent as a function of the ancillary ligands. Spectroelectrochemical (UV/Vis/NIR, EPR) studies along with DFT/TD‐DFT calculations revealed (i) involvement of deprotonated L or HL in the oxidation processes owing to its redox non‐innocent potential and (ii) metal (RuIII/RuII) or bpy/pap dominated reduction processes in 1 + or 2 2+/ 3 +/ 4 2+/ 5 +, respectively. 相似文献
53.
Summary
Bis(cyclopentadienyl)titanium(IV) diisothiocyanate [(Cp)2-Ti(NCS)2] reacts with MCl2 (M = Cu, Pd or Pt), [CuCl(PPh3)3], [RuCl2(PPh3)3] and [RuCl2(DMSO)4] (DMSO = dimethylsulphoxide) giving solid compounds of stochiometry [(Cp)2Ti(-NCS)2MCl2] (M = Cu, Pd or Pt), [(Cp)2Ti(-NCS)2CuCl(PPh3)], [(Cp)2Ti(-NCS)2-RuCl(PPh3)2]Cl and [(Cp)2Ti(-NCS)2RuCl2(DMSO)2]. These products have been characterized by physicochemical and spectroscopic methods. 相似文献
54.
M. Ashraf Chaudry Noor-Ul-Islam Naeem-Ur-Rehman Zafar Yasin 《Journal of Radioanalytical and Nuclear Chemistry》1995,189(2):207-218
The role of nitrate ions in uranyl ions transport across TBP-kerosene oil supported liquid membranes (SLM) at varied concentrations of HNO3 and NaNO3 has been studied. It has been found that nitrate ions move faster compared to uranyl ions at the uranium feed solution concentrations studied. The nitrate to uranyl ions flux ratio vary from 355 to 2636 under different chemical conditions. At low uranium concentration the nitrate ions transport as HNO3 · TBP, in addition to as UO2(NO3)2 · 2TBP type complex species. The flux of nitrate ions is of the order of 12.10 · 10–3 mol · m–2 · s–1 compared to that of uranium ions (4.56 · 10–6 mol · m–2 · s–1). The permeability coefficient of the membrane for nitrate ions varies with chemical composition of the feed solution and is in the order of 2.5 · 10–10 m–2 · s–1. The data is useful to estimate the nitrate ions required to move a given amount of uranyl ions across such an SLM and in simple solvent extraction. 相似文献
55.
V. C. Adya A. Sengupta S. Ansari P. K. Mohapatra M. K. Bhide S. V. Godbole 《Journal of Radioanalytical and Nuclear Chemistry》2013,295(2):1023-1028
Americium from analytical solid waste containing U and metallic impurities was separated using hollow fiber supported liquid membrane (HFSLM) technique impregnated with DHOA–TODGA from nitric acid medium. An aliquot of 5 g of the solid waste containing Am (19.95 mg) as minor actinide and of U (2,588 mg), Fe (1,360 mg), Ca (1,810 mg) and Na (3,130 mg) as major impurities was processed. The feed solution obtained after the dissolution of the residue in ~4 M HNO3 was passed through HFSLM module. In the first stage using 1 M DHOA–dodecane U was recovered while Am and other impurities were left in the raffinate. In the second stage, 0.5 M DHOA + 0.1 M TODGA/dodecane was used for the separation of Am from other impurities. Though, majority of the elements were separated in this cycle, Ca was co extracted along with the americium. CMPO extraction chromatographic technique was used for further separation of americium from Ca. Significant decontamination factors were achieved in this three step separation process with respect to U, Fe, Na and Ca with ~77 % recovery of americium. 相似文献
56.
57.
58.
Zafar A. Siddiqi M. Shahid Mohd Khalid Shabana Noor Sarvendra Kumar 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2010,75(1):61-68
The newly prepared homo-bimetallic complexes [M2(imda)2(H2O)4], [M2(imda)2(Bipy)2] (M = Co, Ni or Cu) and [Fe2(imda)2(H2O)3Cl] (H2imda = iminodiacetic acid and Bipy = 2,2′-bipyridine) have been studied employing IR, FAB-mass, 1H and 13C NMR, EPR and ligand field spectra, which indicated a high-spin state of metal ion with hexa-coordinate environment. 57Fe Mössbauer data of the homo-bimetallic complex [Fe2(imda)2(H2O)3Cl] confirm a high-spin configuration with Fe (±3/2 → 1/2) nuclear transitions and the presence of Kramer's double degeneracy. At RT, the spin–spin interactions of the neighbouring nuclei (Fe3+–Fe3+ = S5/2–S5/2) are anti-ferromagnetically coupled. However, at LNT, the complex acquires a mixed-valent [FeIII–FeII] composition corroborated from the X-band EPR data. CV studies indicated the presence of quasi-reversible redox CuII/I, CuII/III, FeIII/II, FeIII/I and FeII/I couples. 相似文献
59.
Zafar A. Siddiqi Mohd Khalid Sarvendra Kumar M. Shahid Shabana Noor 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2010,75(2):841-845
Spectral and molecular model computations on homo-dinuclear complexes [M2L2(H2O)2Cl2] [L = 1-(salicylaldeneamino)-3-hydroxypropane, M = Cr3+, Mn3+, Fe3+, Co3+, Ni3+ or Cu3+] are consistent with a distorted hexa-coordinate geometry. X-band EPR spectral data indicated a rhombic distortion around Cu(II) ion. Magnetic moment and 57Fe Mössbauer data confirmed a high-spin state electronic configuration (t2g3eg2, S = 5/2) and asymmetric ligand environment around Fe(III) with nuclear transitions Fe(±3/2 → 1/2) exhibiting Kramer's double degeneracy. The neighboring Fe(III) nuclei in the homo-dinuclear species are antiferromagnetically coupled. 相似文献