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Foroutan-Nejad C Shahbazian S Rashidi-Ranjbar P 《Physical chemistry chemical physics : PCCP》2011,13(10):4576-4582
The nature of bonding and aromaticity of Ti(3)(CO)(3), a mill-shaped metal-carbonyl complex, is studied carefully. A unique bonding mechanism between metal and carbonyl groups is found in this species. Ti(3)(CO)(3) is an example of a metal-carbonyl complex with prominent metal to carbonyl donation. Moreover, it is proven that not only is Ti(3)(CO)(3) not an antiaromatic complex but also it is the first synthesized example of d-block, σ+π aromatic species. A quick survey among the first row of transition metals in the periodic table shows that other local minima with similar structures and aromaticity are present and Ti(3)(CO)(3) is the first synthesized species of an unknown family. 相似文献
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Results on a search for Λp, ΛΛ, Λpp, Kop, pp, 3p and 4p resonances are presented. The Λp effective-mass spectrum reveals three significant peaks (more than 4 s.d.) at 2058, 2127 and 2252 MeV. The first two peaks are shown to be due to effects of the negative Λp and Σp scattering lengths respectively, whereas the third peak is interpreted as a Λp resonance of (2251.4 ± 3.9) MeV mass and Λ = (21.1 ± 5.4) MeV full width. The two enhancements observed in the ΛΛ effective-mass spectrum may be due to the effect of the negative ΛΛ scattering length and to a ΛΛ resonance of ~2370 MeV mass. No enhancements in other effective-mass spectra are observed. The results of this work suggest a condition for the possibility of resonance formation depending on the total hypercharge of the system considered. 相似文献
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Central composite design (CCD) and response surface methodology (RSM) were developed as experimental strategies for modeling and optimization of the influence of some variables on the performance of a new PVC membrane triiodide ion-selective electrode. This triiodide sensor is based on triiodide-clozapine ion-pair complexation. PVC, plasticizers, ion-pair amounts and pH were investigated as four variables to build a model to achieve the best Nernstian slope (59.9 mV) as response. The electrode is prepared by incorporating the ion-exchanger in PVC matrix plasticized with 2-nitrophenyl octal ether, which is directly coated on the surface of a graphite electrode. The influence of foreign ions on the electrode performance was also investigated. The optimized membranes demonstrate Nernstian response for triiodide ions over a wide linear range from 5.0 x 10(-6) to 1.0 x 10(-2)mol L(-1) with a limit of detection 2.0 x 10(-6) mol L(-1) at 25 degrees C. The electrodes could be used over a wide pH range 4-8, and have the advantages of easy to prepare, good selectivity and fast response time, long lifetime (over 3 months) and small interferences from hydrogen ion. The proposed electrode was successfully used as indicator electrode in potentiometric titration of triiodide ions and ascorbic acid. 相似文献
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Morteza Bahram Khalil Farhadi Abbas Afkhami Donya Shokatynia Farzin Arjmand 《Central European Journal of Chemistry》2009,7(3):375-381
A partial least squares (PLS-1) calibration model based on kinetic—spectrophotometric measurement, for the simultaneous determination
of Cu(II), Ni(II) and Co(II) ions is described. The method was based on the difference in the rate of the reaction between
Co(II), Ni(II) and Cu(II) ions with 1-(2-pyridylazo)2-naphthol in a pH 5.8 buffer solution and in micellar media at 25°C.
The absorption kinetic profiles of the solutions were monitored by measuring the absorbance at 570 nm at 2 s intervals during
the time range of 0–10 min after initiation of the reaction. The experimental calibration matrix for the partial least squares
(PLS-1) model was designed with 30 samples. The cross-validation method was used for selecting the number of factors. The
results showed that simultaneous determination could be performed in the range 0.1-2 μg mL−1 for each cation. The proposed method was successfully applied to the simultaneous determination of Cu(II), Ni(II) and Co(II)
ions in water and in synthetic alloy samples.
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Gas-chromatographic fatty-acid fingerprints and partial least squares modeling as a basis for the simultaneous determination of edible oil mixtures 总被引:10,自引:0,他引:10
Hajimahmoodi M Vander Heyden Y Sadeghi N Jannat B Oveisi MR Shahbazian S 《Talanta》2005,66(5):1108-1116
Partial least squares modeling and gas-chromatographic fatty-acid fingerprints are reported as a method for the simultaneous determination of cottonseed, olive, soybean and sunflower edible oil mixtures. In this work, two sets of three- and four-component combinations of oils were prepared, hydrolyzed and the obtained free fatty acids analyzed by gas chromatography (GC) without any further derivatization. The normalized percentages of the myristic (14:0), palmitic (16:0), palmitoleic (16:1), stearic (18:0), oleic (18:1), linoleic (18:2) and linolenic (18:3) acids were chromatographically measured in samples and used for constructing calibration matrix. The cross-validation method was used to select the number of factors and the proposed methods were validated by using two sets of synthetic oil mixture samples. The relative standard error for each oil in mixture samples was less than 10%. This approach allows determining possible adulteration in each of the four edible oils. 相似文献
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Juan Andrés Paul W. Ayers Roberto A. Boto Ramon Carbó-Dorca Henry Chermette Jerzy Cioslowski Julia Contreras-García David L. Cooper Gernot Frenking Carlo Gatti Farnaz Heidar-Zadeh Laurent Joubert Ángel Martín Pendás Eduard Matito István Mayer Alston J. Misquitta Yirong Mo Julien Pilmé Paul L. A. Popelier Martin Rahm Eloy Ramos-Cordoba Pedro Salvador W. H. Eugen Schwarz Shant Shahbazian Bernard Silvi Miquel Solà Krzysztof Szalewicz Vincent Tognetti Frank Weinhold Émilie-Laure Zins 《Journal of computational chemistry》2019,40(26):2248-2283
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