排序方式: 共有93条查询结果,搜索用时 15 毫秒
1.
Milway VA Niel V Abedin TS Xu Z Thompson LK Grove H Miller DO Parsons SR 《Inorganic chemistry》2004,43(6):1874-1884
The structures and magnetic properties of self-assembled copper(II) clusters and grids with the "tritopic" ligands 2poap (a), Cl2poap (b), m2poap (c), Cl2pomp (d), and 2pomp (e) are described [ligands derived by reaction of 4-R-2,6-pyridinedicarboxylic hydrazide (R = H, Cl, MeO) with 2-pyridinemethylimidate (a-c, respectively) or 2-acetylpyridine (d, R = Cl; e, R = H)]. Cl2poap and Cl2pomp self-assemble with Cu(NO(3))(2) to form octanuclear "pinwheel" cluster complexes [Cu(8)(Cl2poap-2H)(4)(NO(3))(8)].20H(2)O (1) and [Cu(8)(Cl2pomp-2H)(4)(NO(3))(8)].15H(2)O (2), built on a square [2 x 2] grid with four pendant copper arms, using "mild" reaction conditions. Similar reactions of Cl2pomp and 2pomp with Cu(ClO(4))(2) produce pinwheel clusters [Cu(8)(Cl2pomp-2H)(4)(H(2)O)(8)](ClO(4))(8).7H(2)O (3) and [Cu(8)(2pomp-2H)(4)(H(2)O)(8)](ClO(4))(8) (4), respectively. Heating a solution of 1 in MeOH/H(2)O produces a [3 x 3] nonanuclear square grid complex, [Cu(9)(Cl2poap-H)(3)(Cl2poap-2H)(3)](NO(3))(9).18H(2)O (5), which is also produced by direct reaction of the ligand and metal salt under similar conditions. Reaction of m2poap with Cu(NO(3))(2) produces only the [3 x 3] grid [Cu(9)(m2poap-H)(2)(m2poap-2H)(4)](NO(3))(8).17H(2)O (6) under similar conditions. Mixing the tritopic ligand 2poap with pyridine-2,6-dicarboxylic acid (picd) in the presence of Cu(NO(3))(2) produces a remarkable mixed ligand, nonanuclear grid complex [Cu(9)(2poap-H)(4)(picd-H)(3)(picd-2H)](NO(3))(9).9H(2)O (7), in which aromatic pi-stacking interactions are important in stabilizing the structure. Complexes 1-3 and 5-7 involve single oxygen atom (alkoxide) bridging connections between adjacent copper centers, while complex 4 has an unprecedented mixed micro-(N-N) and micro-O metal ion connectivity. Compound 1 (C(76)H(92)N(44)Cu(8)O(50)Cl(4)) crystallizes in the tetragonal system, space group I, with a = 21.645(1) A, c = 12.950(1) A, and Z = 2. Compound 2 (C(84)H(88)N(36)O(44)Cl(4)Cu(8)) crystallizes in the tetragonal system, space group I, with a = 21.2562(8) A, c = 12.7583(9) A, and Z = 2. Compound 4 (C(84)H(120)N(28)O(66)Cl(8)Cu(8)) crystallizes in the tetragonal system, space group I4(1)/a, with a = 20.7790(4) A, c = 32.561(1) A, and Z = 4. Compound 7(C(104)H(104)N(46)O(56)Cu(9)) crystallizes in the triclinic system, space group P, with a = 15.473(1) A, b = 19.869(2) A, c = 23.083(2) A, alpha = 88.890(2) degrees, beta = 81.511(2) degrees, gamma = 68.607(1) degrees, and Z = 2. All complexes exhibit dominant intramolecular ferromagnetic exchange coupling, resulting from an orthogonal bridging arrangement within each polynuclear structure. 相似文献
2.
Kang IJ Khan NA Haque E Jhung SH 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(23):6437-6442
Chemical and thermal stabilities of isotypic metal-organic frameworks (MOFs) like Al-BDC (Al-benzenedicarboxylate called MIL-53-Al), Cr-BDC (MIL-53-Cr) and V-BDC (MIL-47-V), after purification to remove uncoordinated organic linkers, have been compared to understand the effect of the central metal ions on the stabilities of the porous MOF-type materials. Chemical stability to acids, bases, and water decreases in the order of Cr-BDC>Al-BDC>V-BDC, suggesting stability increases with increasing inertness of the central metal ions. However, thermal stability decreases in the order of Al-BDC>Cr-BDC> V-BDC, and this tendency may be explained by the strength of the metal-oxygen bond in common oxides like Al(2)O(3), Cr(2)O(3), and V(2)O(5). In order to evaluate precisely the stability of a MOF, it is necessary to remove uncoordinated organic linkers that are located in the pores of the MOF, because a filled MOF may be more stable than the same MOF after purification. 相似文献
3.
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
4.
A.S. Ismail S. Zein El Abedin O. Höfft F. Endres 《Electrochemistry communications》2010,12(7):909-911
In this letter we report on the decomposition of the bis (trifluoromethylsulfonyl) amide (TFSA) anion under quite mild electrochemical conditions. The results show clearly that the TFSA anion can easily be decomposed during anodic oxidation of copper in the ionic liquid 1-butyl-1-methylpyrrolidinium bis (trifluoromethylsulfonyl) amide [BMP] TFSA at 70 °C leading to the formation of CuF2. At room temperature, however, no significant decomposition was obtained. Therefore, one has to be very careful in applying ionic liquids based on TFSA anions under anodic conditions at elevated temperature as the TFSA anion might decompose, depending on the anode material. 相似文献
5.
Sherif Zein El Abedin 《Journal of Solid State Electrochemistry》2012,16(2):775-783
The electrochemical behaviors of pure Al, Al–6%Si, Al–3%Cu, and Al–3.7%Cu–0.9%Mg–0.8%Pb–0.6%Fe alloys were investigated in
the chloroaluminate ionic liquids 1-butyl-3-methylimidazolium chloride [BMIm]Cl/AlCl3 (40/60 mol%) and 1-ethyl-3-methylimidazolium chloride [EMIm]Cl/AlCl3 (40/60 mol%). Electrolytic extraction of copper from Al–Cu alloys in the employed ionic liquids was explored. The alloys
were anodically dissolved in the ionic liquids and then pure copper was recovered under potentiostatic conditions. Due to
the large difference between the deposition potentials of Cu and Al, pure Cu can be obtained without Al contamination. Electrorefining
of Al–3%Cu and Al–6%Si alloys was also investigated in [BMIm]Cl/AlCl3 (40/60 mol%) at room temperature. High purity aluminum deposits were obtained with significantly low energy consumption of
about 2 kWh/kg of Al. 相似文献
6.
We discuss the notion of spin squeezing considering two mutually exclusive classes of spin-s states, namely, oriented and non-oriented states. Our analysis shows that the oriented states are not squeezed while non-oriented
states exhibit squeezing. We also present a new scheme for construction of spin-s states using 2s spinors oriented along different axes. Taking the case of s=1, we show that the ‘non-oriented’ nature and hence squeezing arise from the intrinsic quantum correlations that exist among
the spinors in the coupled state. 相似文献
7.
Mohammad Nasir Uddin Zainul Abedin Siddique Nobuyuki Mase Monir Uzzaman Wahhida Shumi 《应用有机金属化学》2019,33(6)
A number of oxotitanium(IV) complexes of the type TiOL with bis‐unsymmetric dibasic tetradentate Schiff base (LH2) containing ONNO donor atoms have been synthesized. Mono‐Schiff base (OPD‐HNP) was prepared by the condensation of 1:3 molar ratio of 2‐hydroxy‐1‐naphthaldehyde (HNP) with o‐phenylenediamine (OPD). Dibasic unsymmetric tetradentate diamine Schiff bases were prepared by the reaction of OPD‐HNP with 2‐hydroxyacetophenone, 2‐hydroxypropeophenone, benzoylacetone, acetylacetone and ethylacetoacetate. Further, titanylacetylacetonate was reacted with these ligands to obtain their metal complexes. On the basis of analytical and physiochemical data, the formation of complexes as TiOL was suggested having square pyramidal geometry. Quantum mechanical approach also confirmed this geometry. The assessment of the synthesized ligands and their complexes showed that some behave as good inhibitors of mycelial growth against selected phytopathogic fungi but weak inhibitors against some selected bacteria. A few of them also showed antioxidant properties. 相似文献
8.
In this paper, we describe a new computer simulation technique of generating Fresnel diffraction images from rectangular apertures of arbitrary dimensions by using Fresnel integrals instead of the more common fast Fourier transform methods. The simulation can be performed in almost any PC using the software MATLAB. Diffraction images can be generated for any wavelength of light and for any aperture–screen and aperture-source distances. Images for rectangular obstacles can also be simulated. Details of the algorithm and program are presented, as well as the interesting insights than can be gained from using the program. Finally, it is shown that the simulated images reduce to the simple Fraunhofer diffraction patterns for certain limiting situations. 相似文献
9.
A. F. M. Y. Haider S. Sengupta K. M. Abedin Aminul I. Talukder 《Applied Physics A: Materials Science & Processing》2011,105(2):487-495
A colloidal solution of gold nanoparticles in deionized nanopure water was produced by laser ablation technique without the
use of any chemical/surfactant. Spectral characterization and morphological studies of these nanoparticles were carried out
by UV-Vis Spectroscopy and Scanning Electron Microscopy, respectively. A number of variables of the ablating laser pulse have
been used to control the size of the fabricated nanoparticles. Excellent correlation between ablating laser pulse parameter
and optical and morphological parameters of the gold colloids were obtained. The peak of the extinction spectra shows a monotonic
blue shift for laser fluence of 410 J/cm2 and above. Below this the extinction peak remains fairly constant in wavelength. Blue shifts of the extinction spectra were
also observed with increasing re-ablation time of previously ablated gold colloids. Possible explanations of all these observations
are discussed. 相似文献
10.