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81.
Utilizing pure amine hydrogen bonding is a novel approach for constructing two‐dimensional (2D) networks. Further, such systems are capable of undergoing structural modifications due to changes in pH. In this study, we designed a 2D network of triaminobenzene (TAB) molecules that by varying the pH from neutral to acidic, form either ordered or disordered structures on Au(111) surface as revealed in scanning tunneling microscopy images. In near‐neutral solution (pH ≈5.5), protonation of TAB generates charged species capable of forming H‐bonds between amine groups of neighboring molecules resulting in the formation of a 2D supramolecular structure on the electrified surface. At lower pH, due to the protonation of the amine groups, intermolecular hydrogen bonding is no longer possible and no ordered structure is observed on the surface. This opens the possibility to employ pH as a chemical trigger to induce a phase transition in the 2D molecular network of triaminobenzene molecules. 相似文献
82.
Shadpour E. Mallakpour Abdol‐Reza Hajipour Ali‐Reza Mahdavian Sepideh Khoee 《Journal of polymer science. Part A, Polymer chemistry》1999,37(8):1211-1219
The reaction of N‐phthaloyl‐L ‐leucine acid chloride (1) with isoeugenol (2) was carried out in chloroform, and novel optically active isoeugenol ester derivative 3 as a chiral monomer was obtained in high yield. Compound 3 was characterized by 1H‐NMR, IR, and mass and elemental analysis and then was used for the preparation of model compound 5 and polymerization reactions. 4‐Phenyl‐1,2,4‐triazoline‐3,5‐dione, PhTD (4), was allowed to react with compound 3. The reaction is very fast and gives only one diastereomer of 5 via Diels–Alder and ene pathways in quantitative yield. In order to explain this diastereoselectivity, a nonconcerted two‐step mechanism involving benzylic cation (BC) and aziridinium (AI) have been proposed for the Diels–Alder and ene reactions, respectively. The polymerization reactions of novel monomer 3 with bis(triazolinedione)s [bis(p‐3,5‐dioxo‐1,2,4‐triazolin‐4‐ylphenyl)methane (8) and 1,6‐bis(3,5‐dioxo‐1,2,4‐triazolin‐4‐yl)hexane] (9)] were performed in N,N‐dimethylacetamide (DMAc) at room temperature. The reactions are exothermic, fast, and gave novel optically active polymers 10 and 11 via repetitive Diels–Alder–ene polyaddition reactions. These polymers have inherent viscosities in a range about 0.18–0.22 dL/g. Some physical properties and structural characterizations of these new polymers have been studied and are reported. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 1211–1219, 1999 相似文献
83.
Bushra Asad Taimoor Khan Faiza Zareen Gul Muhammad Asad Ullah Samantha Drouet Sara Mikac Laurine Garros Manon Ferrier Shankhamala Bose Thibaut Munsch Duangjai Tungmunnithum Arnaud Lanoue Nathalie Giglioli-Guivarch Christophe Hano Bilal Haider Abbasi 《Molecules (Basel, Switzerland)》2021,26(15)
In vitro cultures of scarlet flax (Linum grandiflorum L.), an important ornamental flax, have been established as a new possible valuable resource of lignans and neolignans for antioxidant and anti-inflammatory applications. The callogenic potential at different concentrations of α-naphthalene acetic acid (NAA) and thidiazuron (TDZ), alone or in combinations, was evaluated using both L. grandiflorum hypocotyl and cotyledon explants. A higher callus induction frequency was observed on NAA than TDZ, especially for hypocotyl explants, with a maximum frequency (i.e., 95.2%) on 1.0 mg/L of NAA. The presence of NAA (1.0 mg/L) in conjunction with TDZ tended to increase the frequency of callogenesis relative to TDZ alone, but never reached the values observed with NAA alone, thereby indicating the lack of synergy between these two plant growth regulators (PGRs). Similarly, in terms of biomass, NAA was more effective than TDZ, with a maximum accumulation of biomass registered for medium supplemented with 1.0 mg/L of NAA using hypocotyls as initial explants (DW: 13.1 g). However, for biomass, a synergy between the two PGRs was observed, particularly for cotyledon-derived explants and for the lowest concentrations of TDZ. The influence of these two PGRs on callogenesis and biomass is discussed. The HPLC analysis confirmed the presence of lignans (secoisolariciresinol (SECO) and lariciresinol (LARI) and neolignan (dehydrodiconiferyl alcohol [DCA]) naturally accumulated in their glycoside forms. Furthermore, the antioxidant activities performed for both hypocotyl- and cotyledon-derived cultures were also found maximal (DPPH: 89.5%, FRAP 866: µM TEAC, ABTS: 456 µM TEAC) in hypocotyl-derived callus cultures as compared with callus obtained from cotyledon explants. Moreover, the anti-inflammatory activities revealed high inhibition (COX-1: 47.4% and COX-2: 51.1%) for extract of hypocotyl-derived callus cultures at 2.5 mg/L TDZ. The anti-inflammatory action against COX-1 and COX-2 was supported by the IC50 values. This report provides a viable approach for enhanced biomass accumulation and efficient production of (neo)lignans in L. grandiflorum callus cultures. 相似文献
84.
Kulsoom Ubedullah Abbasi Muhammad Yar Khuhawar Muhammad Iqbal Bhanger 《Chromatographia》2009,70(11-12):1749-1754
Ethyl chloroformate was used as a derivatizing reagent to develop a simple and sensitive gas chromatographic procedure for the determination of tranexamic acid. Analysis was performed on an HP-5 column (30 m × 0.32 mm i.d.) coupled with mass spectrometric detection. Linear response was obtained from 60 to 500 pg with a limit of detection of 20 pg tranexamic acid injected onto the column. Aminocaproic acid was used as an internal standard. Tranexamic acid was determined in pharmaceutical preparations and blood samples after therapy with the drug. Appoximately 2.0 μg mL?1 was found in blood samples. Relative standard deviation for analysis was within 0.1–0.4% (n = 3). Recovery of tranexamic acid added to deprotenized serum was 99.6% with an RSD of 1.2–1.6% (n = 3). Pharmaceutical additives and amino acids, if also present, did not affect the determination. 相似文献
85.
H. Raissi A. F. Jalbout H. Farsi B. Abbasi A. de Leon S. Moghiminia 《International journal of quantum chemistry》2009,109(7):1609-1616
Intramolecular H‐bonds existing for derivatives of 3‐imino‐propenylamine have been studied using the B3LYP/6‐311++G** level of theory. The nature of these interactions, known as resonance‐assisted hydrogen bonds, has been discussed. Vibrational frequencies for α‐derivatives were calculated at the same level of theory. The topological properties of the electron density distributions for N? H···N intramolecular bridges have been analyzed in terms of the Bader theory of atoms in molecules (AIM). Calculation for 3‐imino‐propenylamine derivatives in water solution were also carried out at B3LYP/6‐311++G** level of theory. Finally, the analysis of hydrogen bond in this molecule and their derivatives by quantum theory of natural bond orbital methods fairly support the ab initio results. © 2009 Wiley Periodicals, Inc. Int J Quantum Chem, 2009 相似文献
86.
High sensitive determination of trace amount of cobalt by catalytic adsorptive stripping voltammetry
S. Bahrami S. Abbasi Y. A. Ghorbani A. A. Miran-Beigi 《Russian Journal of Electrochemistry》2009,45(2):208-214
A very sensitive and selective catalytic adsorptive cathodic stripping procedure for trace measurements of cobalt is presented.
The method is based on adsorptive accumulation of cobalt-CCA (calcon carboxylic acid) complex onto a hanging mercury drop
electrode followed by reduction of the adsorbed species by voltammetric scan using differential pulse modulation. The reduction
current is enhanced catalytically by nitrite. The effect of various parameters such as pH, concentration of CCA, concentration
of nitrite, accumulation potential and accumulation time on the selectivity and sensitivity were studied. The optimum condition
for the analysis of cobalt, include pH 5.2 (Acetate buffer), 2.1 μM clacon carboxylic acid, 0.032 M sodium nitrite and an
accumulation potential of 0.05 V (versus Ag/AgCl). Under these optimum conditions and for an accumulation time of 60 s, the
measured peak current at −0.480 V is proportional to the concentration of cobalt over the entire concentration range tested
0.003–2.0 ng ml−1 with a detection limit of 1 pg ml−1 for an accumulation time of 60 s and 2.0–10.0 ng ml−1 for an accumulation time of 40 s. The relative standard deviations for ten replicate measurement of 0.5 ng ml−1 of cobalt were 3.1%. The main advantage of this new system is the microtrace Co(II) determination by ASV. The method was
applied to determination of cobalt in a water sample and some analytical grade salts with satisfactory results.
Published in Elektrokhimiya in Russian, 2009, Vol. 45, No. 2, pp. 221–228.
The article is published in the original. 相似文献
87.
Aliakbar Dehno Khalaji Sepideh Maghsodlou Rad Gholamhossein Grivani Karla Fejfarova Michal Dusek Debasis Das 《Journal of chemical crystallography》2011,41(8):1145-1149
Abstract
Schiff-base compound (E)-4-dimethamino[(1-phenylethyl)iminomethyl]benzyne was synthesized and characterized by elemental analyses (CHN), FT-IR and 1H-NMR spectroscopic techniques and thermogravimetric analyses (TG). Crystal structure of the title compound was obtained by single crystal X-ray diffraction. The title compound crystallizes in the monoclinic space group P21 with unit cell parameters: a = 8.5283(2), b = 6.0699(2), c = 13.6997(4) Ǻ, β = 91.471(2)°, V = 708.94(4) Ǻ3 and Z = 2. 相似文献88.
Sara Nourizadeh Adeleh Divsalar Mina Fekri Behafarid Ghalandari Mahbubeh Eslami-Moghadam Ali Akbar Saboury Saba Abbasi 《Journal of fluorescence》2018,28(2):551-559
In the present study, the biological activities of a new synthesized Pt(II)-complex, 2,2′ bipyridinphenyl isopentylglycin Pt(II) nitrate was investigated via its interaction with the most important blood carrier protein of human serum albumin (HSA), using fluorescence and Far-UV circular dichroism (CD) spectroscopic techniques and also molecular docking. Moreover, cytotoxicity activity of the complex was studied against breast cancer cell line of MDA MB231 using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The Pt(II)-complex has a strong ability to quench the intrinsic fluorescence of HSA through a static quenching mechanism. According fluorescence quenching data, the binding parameters of the interaction were calculated and showed that hydrophobic interaction has an important role. The molecular docking results in coherent with fluorescence measurements illustrated that Pt(II) complex can bind to HSA at one position that located in the hydrophobic cavity of groove between drug site I and II. Also, experimental data on driving force in binding site was confirmed whereas theoretical results demonstrated Pt(II) complexinteract to HSA by hydrophobic interaction. Far-UV-CD results showed that Pt(II)-complex induced an increasing in the content of α-helical structure of the protein and stabilized it. Also, MTT assay represented growth inhibitory effect of the complex toward the breast cancer cell line. 相似文献
89.
Sepideh Ebrahimi Reza Sabbaghi-Nadooshan Mohammad Bagher Tavakoli 《Optical and Quantum Electronics》2018,50(4):196
In this paper, an optical waveguide has been developed based on the (Deoxyribonucleic acid) DNA core as a multi-slab structure by switching characteristic at 300 THz. We show that how the DNA with various electrical characteristics can be considered as a reconfigurable material which is placed between two optical metal layers. Therefore, we can control the current and voltage density values based on the divergence of the DNA types as an optical switch. Moreover, we can select the Au and Ag for the metal coat. In this research, we demonstrate that the Ag/DNA/Ag and Au/DNA/Ag have better performance in switching qualification than Au/DNA/Au model as a conventional structure. This DNA core waveguide has a switchable feature which cannot be found at any conventional plasmonic waveguide. The FDTD time domain is used for simulating the waveguide and the current density is considered as an ON/OFF switch. We carry out parametric studies for the physical dimensions of the waveguide and illustrate that how we can improve the switching characteristic. Moreover, we have checked the coupling effect between the transmission lines and defined the figure of merit for switching quality. This structure can be considered as an optical memristor and optical “YES” gate which couldn’t be obtained by other graphene waveguide while it became feasible based on DNA switching feature. 相似文献
90.
Nowadays, mixed metal oxide (MMO) anodes are a superior alternative to lead alloys in electrowinning processes. Passivation of titanium substrate is the most common mechanism of deactivation in these anodes. In this research, titanium oxide nanotubes have been utilised as an interlayer between the substrate and a mixed metal oxide coating in order to improve the anode electrochemical behaviour and life via retardation of titanium passivation. Anodising of the substrate was done in 0.5 wt% hydrofluoric acid for 30, 60 and 240 min. The samples were subsequently coated with a coating composed of IrO2-RuO2-Ta2O5. The microstructure of different samples was observed by scanning with an electron microscope, and the electrochemical behaviour of the samples was studied by accelerated life test, cyclic voltammetry and electrochemical impedance spectroscopy. The studies showed that formation of titanium oxide nanotubes with anodising times of 60 and 240 min increases the life of the anode through the provision of a compact coating. The life of the anode which was anodised for 240 min lasted about 20% longer than the sample which had a substrate without any anodised layer. 相似文献