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1.
Mahbod Morshedi Soraia Meghdadi Kurt J. Schenk 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(3):m87-m89
The quinquedentate ligand 2,2′‐[1,1′‐(4‐azaheptane‐1,7‐diyldinitrilo)diethylidyne]diphenol in the title compound, [Cu(C22H27N3O2)], furnishes an N3O2 donor set, which results in a distorted square‐pyramidal coordination; the two O and two imine N atoms lie in the basal plane, while the secondary amine N atom of the ligand occupies the axial position. The axial Cu—N bond is 0.33 Å longer than the average of the equatorial bonds, and the O atoms are trans. The symmetry of the molecule is lowered by the twist–boat and chair conformations adopted by the two CuNN chelate rings. The complex contains two intramolecular C—H⋯O interactions, and two molecules of the complex are linked into a dimer by means of moderate N—H⋯O hydrogen bonds. Spectroscopic evidence supports the presence of hydrogen bonds. 相似文献
2.
Mahsa Kiani Mojtaba Bagherzadeh Soraia Meghdadi Farzaneh Fadaei-Tirani Maryam Babaie Kurt Schenk-Joß 《应用有机金属化学》2020,34(11):e5911
The new Co(II) - carboxamide complex ( 1 ) and Co3O4 nanoparticles ( 2 ), by way of thermal decomposition of ( 1 ) have been efficiently synthesised in the environment-friendly. X-ray diffraction reveals a slightly distorted octahedral coordination of cobalt (four nitrogens and two oxygens) in ( 1 ) and regular octahedral or tetrahedral ones (oxygens only) in ( 2 ). The investigation of ( 1 ) and ( 2 ) in the Mizoroki-Heck and epoxidation of alkens reactions showed them both to be powerful, green and inexpensive catalysts. 相似文献
3.
Paula Gomes Maria João Araújo Eduardo F. Marques Soraia Falcão Rodrigo O. Brito 《合成通讯》2013,43(12):2025-2036
Double-chained surfactants with potential biocompatibility have been prepared in high yields by lysine acylation with four natural saturated fatty acids (C6 to C12) and with cis-undec-5-enoic acid. The surfactants were found to assemble into nanotubules in aqueous medium and, when mixed with a commercial cationic surfactant, to spontaneously form liposomes. 相似文献
4.
Mohammad Saraji Hamideh Yousefi Soraia Meghdadi 《International journal of environmental analytical chemistry》2013,93(5):305-317
An ion imprinted silica sorbent was prepared using a sol–gel process for selective extraction of Ni(II) ions from water samples. Bis(dibenzoylmethanto)nickel(II) complex was used as template; phenyltrimethoxysilane and 3-aminopropyltriethoxysilane as functional monomers and tetraethylorthosilicate as reticulating agent. The material was packed in solid-phase extraction (SPE) column. The effect of sampling volume, elution conditions, sample pH and sample flow rate on the extraction of Ni ions from water samples were studied. The relative selectivity coefficients of imprinted sorbent for Ni(II)/Co(II), Ni(II)/Cu(II) and Ni(II)/Cd(II) were 23.7, 30.3 and 24.4, times greater than non-imprinted sorbent, respectively. The relative standard deviation of the eight replicate determinations of Ni(II) was 4.2%. The detection limit was 0.9 µg L?1 using flame atomic absorption spectrometry. The developed method was successfully applied to the determination of trace nickel in water samples. 相似文献
5.
Soraia Meghdadi Mehdi Amirnasr Maryam Bagheri Fatemeh Ahmadi Najafabadi Kurt Mereiter Kurt Joß Schenk Fahimeh Ziaee 《Journal of the Iranian Chemical Society》2014,11(4):985-991
Nickel(II) and copper(II) complexes of two unsymmetrical tetradentate Schiff base ligands [Ni(Me-salabza)] (1), [Cu(Me-salabza)] (2) and [Ni(salabza)] (3), {H2salabza = N,N′-bis[(salicylidene)-2-aminobenzylamine] and H2Me-salabza = N,N′-bis[(methylsalicylidene)-2-aminobenzylamine]}, have been synthesized and characterized by elemental analysis and spectroscopic methods. The crystal structures of 2 and 3 complexes have been determined by single crystal X-ray diffraction. Both copper(II) and nickel(II) ions adopt a distorted square planar geometry in [Cu(Me-salabza)] and [Ni(salabza)] complexes. The cyclic voltammetric studies of these complexes in dichloromethane indicate the electronic effects of the methyl groups on redox potential. 相似文献
6.
Soraia Meghdadi Kurt Mereiter Ahmad Amiri Narges S. Mohammadi Fahimeh Zamani Mehdi Amirnasr 《Polyhedron》2010
A novel and highly efficient approach for the synthesis of H2Me2bqb and H2Me2bpb using ionic liquid as an environmentally benign reaction medium has been developed, eliminating the need for the pyridine as a toxic solvent. The Ni(II) complex of the dianionic ligand Me2bqb2−, [Me2bqb2− = 1,2-bis(quinoline-2-carboxamide)-4,5-dimethyl-benzene dianion], has been synthesized and characterized by elemental analyses and spectroscopic methods, and the crystal and molecular structure of [Ni(Me2bqb)] (1), has been determined by X-ray crystallography. The complex exhibits distorted square-planar NiN4 coordination geometry with two short and two long Ni–N bonds (Ni–N ∼1.85 and ∼1.96 Å, respectively). The electrochemical behavior of [Ni(Me2bqb)] (1), has been studied by cyclic voltammetry and compared with the analogous complex, [Ni(Me2bpb)] (2). 相似文献
7.
A. L. M. de Oliveira J. M. Ferreira Márcia R. S. Silva Soraia C. de Souza F. T. G. Vieira E. Longo A. G. Souza Iêda M. G. Santos 《Journal of Thermal Analysis and Calorimetry》2009,97(1):167-172
NiWO4 and ZnWO4 were synthesized by the polymeric precursor method at low temperatures with zinc or nickel carbonate as secondary phase.
The materials were characterized by thermal analysis (TG/DTA), infrared spectroscopy, UV–Vis spectroscopy and X-ray diffraction.
NiWO4 was crystalline after calcination at 350 °C/12 h while ZnWO4 only crystallized after calcination at 400 °C for 2 h. Thermal decomposition of the powder precursor of NiWO4 heat treated for 12 h had one exothermic transition, while the precursor heat treated for 24 h had one more step between
600 and 800 °C with a small mass gain. Powder precursor of ZnWO4 presented three exothermic transitions, with peak temperatures and mass losses higher than NiWO4 has indicating that nickel made carbon elimination easier. 相似文献
8.
The solid state thermal behavior of trans-[Co(bpb)(amine)2]NCS⋅H2O complexes where (bpb)=[N,N’-bis(2-pyridinecarboxamido-N)-1,2-benzene], and amine=pyrrolidine (prldn)(1), and benzylamine (bzlan) (2), and trans-[Co(bpb)(piperidine)2]ClO4⋅H2O (3) (mixed with KSCN), has been studied using thermoanalytical techniques, infrared spectroscopy, and pyrolysis coupled
to both infrared and mass spectrometry, PY/FTIR and PY/MS. The deamination-anation reaction is clearly observed for all three
complexes. The estimated values of E
a for the deamination-anation are: E
a(1)=246.8 kJ mol−1, E
a(2)=255.7 kJ mol−1, E
a(3)=234.7 kJmol−1. The trend in E
a values is rationalized based on the ligand field strength of the amines and the structural effects. A novel decarbonylation
of the amide CO group from the equatorial ligand is observed after the release of one amine molecule. This process has been
monitored for complex (1) by FTIR in the carbonyl region and by mass spectrometry for the detection of CO2 at 280°C. The activation energy of this process is estimated for complex (1) (662.5 kJ mol−1). The reaction scheme for the observed reactions is proposed.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
9.
In this article we have discussed the E-convex functions and studied the theorems of Jensen, Bernstein–Doetsch, Blumberg–Sierpinski and Ostrowski on E-midconvex functions. 相似文献