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11.
Duymus H Arslan M Kucukislamoglu M Zengin M 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2006,65(5):1120-1124
Charge transfer (CT) complexes of some non-steroidal anti-inflammatory drugs, naproxen and etodolac which are electron donors with some pi-acceptors, such as tetracyanoethylene (TCNE), 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ), p-chloranil (p-CHL), have been investigated spectrophotometrically in chloroform at 21 degrees C. The coloured products are measured spectrophotometrically at different wavelength depending on the electronic transition between donors and acceptors. Beer's law is obeyed and colours were produced in non-aqueous media. All complexes were stable at least 2 h except for etodolac with DDQ stable for 5 min. The equilibrium constants of the CT complexes were determined by the Benesi-Hildebrand equation. The thermodynamic parameters DeltaH, DeltaS, DeltaG degrees were calculated by Van't Hoff equation. Stochiometries of the complexes formed between donors and acceptors were defined by the Job's method of the continuous variation and found in 1:1 complexation with donor and acceptor at the maximum absorption bands in all cases. 相似文献
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Yasemin Yahsi Elif Gungor M. Burak Coban Hulya Kara 《Molecular Crystals and Liquid Crystals》2016,637(1):67-75
A new linear trinuclear MnIII-MnII-MnIII complex 1 has been synthesized and characterized by elemental, spectral, X-ray and magnetic analysis. X-ray diffraction studies show that the central MnII ion is located at a crystallographic inversion center and is triply bridged to the terminal MnIII ions through one methoxide, one syn-syn carboxylate and one hydroxyl oxygen bridges with the short MnIII…MnII distance that is 3.047 Å. The intermolecular C-H…O, C-H…π and ring-metal interactions are observed in the hydrogen-bonded assembly of 1. Magnetic studies reveal that the mixed-valence complex 1 has S = 3/2 ground state with antiferromagnetic exchange interactions between MnII and MnIII ions. 相似文献
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In this paper, sub equation and expansion methods are proposed to construct exact solutions of a nonlinear longitudinal wave equation (LWE) in a magneto-electro-elastic circular rod. The proposed methods have been used to construct hyperbolic, rational, dark soliton and trigonometric solutions of the LWE in the magneto-electro-elastic circular rod. Arbitrary values are given to the parameters in the solutions obtained. 3D, 2D and contour graphs are presented with the help of a computer package program. Solutions attained by symbolic calculations revealed that these methods are effective, reliable and simple mathematical tool for finding solutions of nonlinear evolution equations arising in physics and nonlinear dynamics. 相似文献
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Hudlicky T Rinner U Gonzalez D Akgun H Schilling S Siengalewicz P Martinot TA Pettit GR 《The Journal of organic chemistry》2002,67(25):8726-8743
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Hulya Silah Sedat Ture 《Phosphorus, sulfur, and silicon and the related elements》2013,188(2):198-214
Abstract The reactions of hexachlorocyclotriphosphazene, N3P3Cl6 (1), with 2,2-dimethylpropane-1,3-diol (2), and bis(2-hydroxyethyl) ether (3) have been previously reported. Although both reactions gave the expected spiro, ansa, and bridged type products, open-chain and triply bridged derivatives from both systems and singly bridged derivatives from 2,2-dimethylpropane-1,3-diol (2) were not isolated, and doubly bridged compounds were only detected in trace amounts in both systems. However, in a subsequent reinvestigation in tetrahydrofuran (THF) solution, the reaction of 1 with the diols 2 and 3 gave the open chain compounds N3P3Cl5[O(CH2)2CMe2OH] (4) and N3P3Cl5[(OCH2CH2)2OH] (5), the singly bridged compound N3P3Cl5[(OCH2)2-CMe2]N3P3Cl5 (6), the doubly bridged compounds N3P3Cl4[(OCH2)2CMe2]2N3P3Cl4 (8) and N3P3Cl4[(OCH2CH2)2O]2N3P3Cl4 (9), and the triply bridged compounds N3P3Cl3[(OCH2)2-CMe2]3N3P3Cl3 (10) and N3P3Cl3[(OCH2CH2)2O]3N3P3Cl3 (11). The doubly bridged derivatives were also isolated in better yields relative to earlier reports. The substituted cyclotriphosphazenes have been characterized by elemental analysis, mass spectrometry, as well as by 1H, 31P, and 13C NMR spectroscopy. It is found that with variation of the solvent there is a decrease in the product formed by intramolecular reactions (spiro and ansa derivatives) and a concomitant increase in the amount of products formed by intermolecular reactions (singly, doubly, and triply bridged derivatives) of cyclophosphazene. 相似文献
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Iron and copper are essential nutrients for all living organisms as cofactors of many enzymes and play important roles in electron transport system (ETS) enzymes which have heme and iron–sulfur centers. In the present study, ETS enzymes, namely, succinate dehydrogenase (SDH) and cytochrome c oxidase (COX), activities as well as adenine nucleotides and lipid peroxidation (LPO) levels of eukaryotic model Trichoderma harzianum grown in varied concentrations of iron (0–20 mg/l) and copper (0–25 mg/l) mediums have been examined. SDH and COX activities increased up to 10 mg/l of iron. COX and SDH activities increased significantly up to 15 and 1 mg/l of copper, respectively. ATP and ADP levels showed a positive correlation with SDH activity with respect to iron–copper concentrations. The trends of AMP were similar with those of ATP and ADP for iron concentrations, while AMP levels elevated until 5 mg/l of copper. As an indicative marker of membrane damage, LPO levels increased with iron and copper concentration. In conclusion, iron and copper concentrations are of critical importance on activities of the ETS enzymes besides adenine nucleotides and LPO levels by maintenance of this metal homeostasis. 相似文献
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Gungor E Kara H 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2011,82(1):217-220
A new hydrogen-bonded pseudo-dimer, [Mn(III)L1(CH3CH2OH)]2(ClO4) (1) (L1 = N,N′-bis(2-hydroxy-1-naphthalidenato)-1,2-diaminopropane) has been synthesized and characterized by UV–vis, IR, elemental analysis and crystal structure analysis. The single crystal X-ray diffraction reveals that the structure affords an elongated octahedral MnN2O4 coordination environment, geometry with the four donor atoms of the tetradentate Schiff base in the equatorial plane and with two ethanol molecule in axial positions with Mn–O = 2.265(2) and 2.266(2) Å. 相似文献
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Fatma Cavus Yonar Gulten Rayimoglu Beril Anilanmert Emel Hulya Yukseloglu Salih Cengiz 《Electrophoresis》2022,43(3):425-436
The questions on which judges/prosecutors apply for expertise are mostly about by whom a document was drafted/signed. In this study, a new collective strategy was constructed including a collection method, a modified-silica-based DNA isolation method, and a novel purification method on four contact traces formed on four different paper surface during writing, using PCR with AmpFlSTR®GlobalFiler™ STR kit (after experimental comparison between three different kits) and identification using CE. This collective analysis approach is more sensitive and superior to its equivalents on questioned documents in literature because quantifiable amounts of touch DNA and profiles with high loci percentages (100% on day 1, 72.72% after 1 week) were obtained up to 1 week even after the most challenging conditions of sample forming that a forensic scientist can meet; as washing hands just before drafting and using a very low pressure in a shorter time (simulating a simple contact real conditions while drafting), using no visualizing technique that damages the document. Using the strategy, four most commonly used paper types were compared, to see in which of them DNA could be recovered better. The success of this strategy was shown on the 1-day to 10-year-old real samples from a diary and some archive documents from a law office (including the mix-DNA and different ballpoint pens). Thus, it became possible to show if a person had touched the document, in high success rates up to 1 week as a secondary evidence, when primary evidences are insufficient for the detection of document fraud offenses. 相似文献
20.
Arslan M Duymus H 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2007,67(3-4):573-577
Charge transfer complexes between colchicine as donor and pi acceptors such as tetracyanoethylene (TCNE), 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ), p-chloranil (p-CHL) have been studied spectrophotometrically in dichloromethane at 21 degrees C. The stoichiometry of the complexes was found to be 1:1 ratio by the Job method between donor and acceptors with the maximum absorption band at a wavelength of 535, 585 and 515 nm. The equilibrium constant and thermodynamic parameters of the complexes were determined by Benesi-Hildebrand and van't Hoff equations. Colchicine in pure form and in dosage form was applied in this study. The formation constants for the complexes were shown to be dependent on the structure of the electron acceptors used. 相似文献