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41.
Let Δ be a simplicial complex and χ be an s-coloring of Δ. Biermann and Van Tuyl have introduced the simplicial complex Δχ. As a corollary of Theorems 5 and 7 in their 2013 article, we obtain that the Stanley–Reisner ring of Δχ over a field is Cohen–Macaulay. In this note, we generalize this corollary by proving that the Stanley–Reisner ideal of Δχ over a field is set-theoretic complete intersection. This also generalizes a result of Macchia. 相似文献
42.
Shabnam Fakhari Azita Nouri Mina Jamzad Samira Arab‐Salmanabadi Foujan Falaki 《中国化学会会志》2021,68(1):67-75
In this study, the density functional theory computational method is used to investigate the encapsulation process of metformin into three types of the cyclic peptides composed of eight serine (CP1), eight glycine (CP2), and four serine‐glycine (CP3) cyclic peptides as a new model in the process of drug delivery in the gas phase. The obtained results using the B3LYP/6‐31++G (d,p) method indicate that the complexes formed are energetically favored. Furthermore, results reveal that the drug encapsulation process is typically chemisorption. The natural bonding orbital analysis shows that the intermolecular interaction of the C2 complex (metformin/CP2) is stronger than the C1 (Metformin/CP1) and C3 (Metformin/CP3) complexes due to greater total charge transfer energy, and the C1 complex is found to be the most favored complex. The theory of atoms in molecule (AIM) method is used to analyze the nature of interactions in different molecular systems. The results show the investigated cyclic peptides as effective carriers of metformin in the nanomedicine field. 相似文献
43.
S. Makarem A. R. Fakhari Ali A. Mohammadi 《Monatshefte für Chemie / Chemical Monthly》2009,140(6):645-649
Abstract Electrochemical oxidation of 2,3-dimethylhydroquinone has been studied in the presence of β-diketones as nucleophiles in aqueous
solution using cyclic voltammetry and controlled-potential coulometry. The results indicate that the derivatives of 2,3-dimethylhydroquinone
participate in a Michael addition reaction to form the corresponding benzofuran derivatives. The electrochemical synthesis
has been successfully performed at pH 7.0 and E = 0.1 V versus an Ag|AgCl|KCl (3 M) in an undivided cell in good yield and purity.
Graphical Abstract
相似文献
44.
S. Makarem A. R. Fakhari Ali A. Mohammadi 《Monatshefte für Chemie / Chemical Monthly》2009,38(12):645-649
Abstract
Electrochemical oxidation of 2,3-dimethylhydroquinone has been studied in the presence of β-diketones as nucleophiles in aqueous solution using cyclic voltammetry and controlled-potential coulometry. The results indicate that the derivatives of 2,3-dimethylhydroquinone participate in a Michael addition reaction to form the corresponding benzofuran derivatives. The electrochemical synthesis has been successfully performed at pH 7.0 and E = 0.1 V versus an Ag|AgCl|KCl (3 M) in an undivided cell in good yield and purity. 相似文献45.
Non-aqueous capillary electrophoresis was evaluated for the separation of five hydrophobic basic blue dyes for application in forensic dye analysis. The use of a red light emitting diode as a high intensity, low-noise light source provided sensitive detection of the blue dyes while also allowing the evaluation of solvents that absorb strongly in the UV region. Excellent peak shapes and separation selectivity were obtained in methanol, ethanol, acetonitrile and dimethylsulfoxide, however water, tetrahydrofuran, dimethylformamide and acetone were unsuitable as solvents due to poor peak shapes and a lack of sensitivity, most likely due to adsorption onto the capillary wall. Due to the known compatibility of methanol with capillary electrophoresis–mass spectrometry, this solvent was examined further with the relative acidity/basicity of the electrolyte being optimised with an artificial neural network. The optimised method was examined for the separation of ink samples from 6 fibre tip and 2 ball point blue or black pens and showed that a unique migration time for the main dye component in seven of the eight pens could be obtained. 相似文献
46.
Abstract
In this study, we present a convenient and efficient method for the synthesis of novel, highly substituted 2-vinyl furans using a three-component reaction. The zwitterions generated from the reaction of isocyanides and dialkyl acetylenedicarboxylates are reacted with trans-cinnamoyl chlorides to produce the desired products in good yields. 相似文献47.
48.
Evaluation of sulfated maltodextrin as a novel anionic chiral selector for the enantioseparation of basic chiral drugs by capillary electrophoresis 下载免费PDF全文
Hadi Tabani Mojtaba Mahyari Ali Sahragard Ali Reza Fakhari Ahmad Shaabani 《Electrophoresis》2015,36(2):305-311
Introducing a new class of chiral selectors is an interesting work and this issue is still one of the hot topics in separation science and chirality. In this study, for the first time, sulfated maltodextrin (MD) was synthesized as a new anionic chiral selector and then it was successfully applied for the enantioseparation of five basic drugs (amlodipine, hydroxyzine, fluoxetine, tolterodine, and tramadol) as model chiral compounds using CE. This chiral selector has two recognition sites: a helical structure and a sulfated group which contribute to three corresponding driving forces; inclusion complexation, electrostatic interaction, and hydrogen binding. Under the optimized condition (buffer solution: 50 mM phosphate (pH 3.0) and 2% w/v sulfated MD; applied voltage: 18 kV; temperature: 20°C), baseline enantioseparation was observed for all mentioned chiral drugs. When instead of sulfated MD neutral MD was used under the same condition, no enantioseparation was observed which means the resolution power of sulfated MD is higher than neutral MD due to the electrostatic interaction between sulfated groups and protonated chiral drugs. Also, the countercurrent mobility of negatively charged MD (sulfated MD) allows more interactions between the chiral selector and chiral drugs and this in turn results in a successful resolution for the enantiomers. Furthermore, a higher concentration of neutral MD (approximately five times) is necessary to achieve the equivalent resolution compared with the negatively charged MD. 相似文献
49.
The fluorescence of a new aminocyanonaphthalene exhibits exquisite sensitivity to its environment and responds to a solvent change from water to hexane with greater than a 100-fold increase in intensity and 100 nm shift in λ(max.em). These properties should support many applications including the detection of abasic sites within duplex DNA as illustrated below. 相似文献
50.
Mohammadreza Mohammadi Nilash Sajad Avar Fahimeh Mirzaei Ali Reza Fakhari Abbas Rezaee Shirin‐abadi 《Journal of separation science》2020,43(5):920-928
The present study deals with the synthesis and electrospining of a new terpolymer nanofiber in order to determine the amount of diazinon and chlorpyrifos in water and fruit juice samples. The synthesized terpolymer and the prepared nanofiber were characterized using 1H NMR spectroscopy, FTIR spectroscopy, scanning electron microscopy, and gel permeation chromatography. The performance of terpolymer nanofiber, prepared as a sorbent for micro solid phase extraction was investigated for the extraction of diazinon and chlorpyrifos from aquaeous media. Then, the target analytes were desorbed from the coating with an organic solvent and analyzed by gas chromatography with flame ionization detector. Extraction efficiencies were significant (>90%) under the optimum condition. The proposed method also demonstrated good linear dynamic ranges for diazinon and chlorpyrifos (3–250 and 5–200 µg/L), and low limit of detections (0.5 and 0.7 µg/L) respectively. Moreover, under optimum condition for extraction of diazinon and chlorpyrifos, square of correlation coefficients (R2) of 0.9978 and 0.9953 and relative standard deviations of 4.6 and 5.1% were achieved, respectively. The recoveries for diazinon and chlorpyrifos were in the range of 85–97%. 相似文献