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101.
Fatih Ozaydin Azmi Ali Altintas Sinan Bugu Can Yesilyurt Metin Arik 《International Journal of Theoretical Physics》2014,53(9):3219-3225
We study the quantum Fisher information (QFI) of a system of several particles which is in a superposition of a GHZ and two W states with arbitrary relative phase. We show that as the number of particles increases from 3 to 4, the behavior of QFI drastically changes. We also show how the dependence of QFI on the relative phase weakens as the number of particles increases. We also analyze the QFI for the state for several instances of N due to the change of the relative phases. 相似文献
102.
Duygu S. Esen Gokhan Temel Demet K. Balta Xavier Allonas Nergis Arsu 《Photochemistry and photobiology》2014,90(2):463-469
Acetic acid–based thioxanthone (TXCH2COOH) was synthesized and characterized and used as a photoinitiator for free radical photopolymerization of methyl methacrylate (MMA) in the absence and presence of a tertiary amine (MDEA) in different solvents. Different absorption properties were observed depending on the solvent. Fluorescence and phosphorescence experiments were also carried out successfully. The fluorescence quantum yield was found to be 0.09 and the phosphorescence lifetime was calculated as 138 ms at 77 K. The photoinitiator undergoes efficient intersystem crossing into the triplet state and the lowest triplet state possesses π–π* configuration. Laser flash photolysis experiments show that transient absorption of TXCH2COOH is similar to the parent thioxanthone and the triplet lifetime was calculated as 2.3 μs at 630 nm. 相似文献
103.
A series of N‐(5‐methyl‐2‐hydroxyphenyl)‐(2/3/4/5‐substituted)‐benzaldimines ( I – XIII ) were synthesized using appropriate synthetic route. Their structures were characterized by FT‐IR, UV‐Visible, ESI‐MS, 1H‐ and 13C‐NMR spectroscopic techniques and analytical methods. The crystal structure of N‐(5‐methyl‐2‐hydroxyphenyl)‐3,4‐dimethoxybenzaldimine ( XIII ) was determined by X‐ray diffraction at room temperature. Relationship between the melting points and the structures of the compounds were examined. Antibacterial activities of the compounds were evaluated against Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa and Proteus mirabilis. Antifungal activities were reported for Candida albicans. Some of the Schiff bases showed considerable antimicrobial activity against S. aureus and C. albicans. 相似文献
104.
Alper Tolga olak Ferda olak Demet Akduman Okan Zafer Yeilel Orhan Büyükgüngr 《Solid State Sciences》2009,11(11):1908-1918
In this study, three novel Cu(II)-pyridine-2,5-dicarboxylate (pydc) complexes with 4-methylimidazole (4-Meim), [Cu(pydc)(H2O)(4-Meim)2]·H2O (1), imidazole (im), {[Cu(μ-pydc)(im)2]·2H2O}n (2), and 3,4-dimethylpyridine (dmpy), [Cu(μ-pydc)(H2O)(dmpy)]n (3) have been synthesized. Elemental and thermal analyses, magnetic susceptibilities, IR and UV/vis spectroscopic studies have been performed to characterize the complexes. The molecular structures of mononuclear (1) and polynuclear (2 and 3) complexes have been determined by the single crystal X-ray diffraction technique. In 1 and 2, Cu(II) ions have distorted square planer geometry, while 3 has distorted octahedral coordination. The pyridine-2,5-dicarboxylate exhibits three different coordination modes namely bidentate (1), tridentate (2) and tetradentate (3). The complex 1 is further constructed to form three-dimensional framework by hydrogen bonding, C–Hπ and ππ stacking interactions. The adjacent chains of 2 and 3 are then mutually linked via hydrogen bonding, ππ and C–Hπ interactions, which are further assembled to form three-dimensional framework. 1 exhibits the magnetic moment value of 1.70 BM, which corresponds to one of the unpaired electron, while the polynuclear complexes 2 and 3 exhibit 1.58 and 1.46 BM, which is lower than the spin only value for one unpaired electron, indicates to antiferromagnetic effect. The first thermal decomposition process of all the complexes is endothermic dehydration. This stage is followed by partial (or complete) decomposition of the neutral and pydc ligands. In the later stage, the remained organic residue exothermically burns. The final decomposition products which identified by IR spectroscopy were the CuO. 相似文献