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101.
Grochowicz Marta Pączkowski Przemysław Gawdzik Barbara 《Journal of Thermal Analysis and Calorimetry》2018,133(1):499-508
Journal of Thermal Analysis and Calorimetry - The study describes the thermal properties of functional microspheres composed of glycidyl methacrylate (GMA) and crosslinking agent ethylene glycol... 相似文献
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Chloroplast reorientations within mesophyll cells are among the most rapid physiological responses of higher plants to blue light. At light intensities below the saturation point of photosynthesis, chloroplasts move to the cell walls perpendicular to the direction of light and maximize light absorption (low-fluence rate response [LFR]). At light intensities above the saturation point of photosynthesis, chloroplasts redistribute to cell walls parallel to the direction of light (high-fluence rate response [HFR]). The actin-based mechanism is responsible for the light-induced chloroplast movements. We have found that an inhibitor of phosphoinositide-3-kinases, wortmannin, potently and irreversibly inhibited LFR and HFR chloroplast responses to blue light in Lemna trisulca L. mesophyll cells. Microscopic observations and photometric measurement indicated that 100 nM wortmannin specifically inhibited LFR in Lemna, whereas HFR displayed no sensitivity to the inhibitor at this concentration. A complete inhibition of the HFR could be obtained by 1 microM wortmannin. These data indicate that LFR is more sensitive to wortmannin than HFR and suggest that these two responses may be under the control of different cellular mechanisms. Our results suggest that phosphoinositide kinases and other phosphoinositide cycle enzymes may play a role in the transduction of the light signal to the actin cytoskeleton in Lemna as factors specifying the direction of chloroplast movements. A hypothetical model assuming three signaling pathways regulating light-induced chloroplast reorientations in mesophyll cells is proposed. 相似文献
105.
The absorption, fluorescence excitation, and fluorescence emission spectra of water solutions of fluorescein dye with the addition of various amounts of a colloidal silver suspension have been measured in order to check if in such systems it is possible to distinguish the change in photonic mode density due to the metal presence from the other effects such as the influences of the microemulsion system on the spectral properties of the dye. It has been found that the presence of the silver colloid changes the concentrations of the various ionic forms of fluorescein, characterized by different yields of fluorescence. This effect is partially responsible for the change in the yield of the fluorescence emission observed at certain concentrations of the dye and the colloids. But even at the same concentration of various ionic forms of fluorescein (at the same pH of the dye solution and the dye-colloid mixture), at certain concentrations of fluorescein and the colloid, the yield of the dye fluorescence increases, which must be due to the interaction between the dye and the silver colloid. Because of the superposition of several processes influencing the dye yield of fluorescence, it is necessary to carefully establish the properties of the dye in a given environment, before considering its practical application as a marker of the metal presence. It is not excluded that similar complex effects could also occur in biological samples containing natural pigments and colloids of metals. Investigations of other dyes with other forms of metallic samples are in progress. 相似文献
106.
Dr. Przemysław J. Malinowski Dr. Daniel Himmel Prof. Dr. Ingo Krossing 《Angewandte Chemie (International ed. in English)》2016,55(32):9259-9261
The perfluorohexane‐soluble and donor‐free silver compound Ag( A ) ( A =Al(ORF)4; RF=C(CF3)3) prepared using a facile novel route has unprecedented capabilities to form unusual and weakly bound complexes. Here, we report on the three dihalogen–silver complexes Ag(Cl2) A , Ag(Br2) A , and Ag(I2) A derived from the soluble silver compound Ag( A ) (characterized by single‐crystal/powder XRD, Raman spectra, and quantum‐mechanical calculations). 相似文献
107.
Experimental versus Calculated Proton Affinities for Aromatic Carboxylic Acid Anions and Related Phenide Ions 下载免费PDF全文
Herein, we present the comparison of a large set of experimentally measured proton affinity (PA) values for 65 aromatic carboxylate anions with the values calculated by using selected popular DFT (B3LYP, PBE0, and M05‐2X) and composite [G3(MP2), G4(MP2)] quantum chemistry methods. The root‐mean‐square error (RMSE) values for the chosen methods are RMSEPBE0=1.7, RMSEB3LYP=4.6, RMSEM05‐2X=6.6, RMSEG3MP2=6.3, RMSEG4MP2=4.5 kJ mol?1. In the second part of the study, 82 PA values for substituted phenide ions and a few heteroaromatic anions were calculated. Again, very good agreement between the calculated and experimental values has been observed: RMSEPBE0=1.9, RMSEB3LYP=4.5, RMSEM05‐2X=6.3, RMSEG3MP2=4.9, RMSEG4MP2=5.5 kJ mol?1. Our results show that, for medium‐sized carboxylate anions, all tested methods give reliable results and, surprisingly, much more computationally demanding composite methods do not perform significantly better than the time‐efficient DFT methods. 相似文献
108.
Developments in the chemistry of weakly coordinating anions enabled isolation of numerous unique metal complexes with unusual ligands. An important example is the family of metal-Fe(CO)5 complexes. In the current paper we present synthesis and thorough characterization of the first truly homoleptic {Cu[Fe(CO)5]2}+ cation obtained as a salt of weakly coordinating [Al(ORF)4]− (RF=C(CF3)3) anion. TGA/DSC/MS study show that its decomposition becomes noticeable only above 110 °C, thus it can be stored as powder in air-free conditions for months. The crystal structure of {Cu[Fe(CO)5]2}+ shows strong asymmetry of the cation and very short Cu-CO bonds in comparison to analogous {M[Fe(CO)5]2}+ where M=Ag or Au. Characterization is complemented with analysis of vibrational spectra and extensive DFT calculations which give insight into the energetics of Cu+-Fe(CO)5 systems. Our results show that {Cu[Fe(CO)5]2}+ is homoleptic only as salt of [Al(ORF)4]−. Furthermore, in the presence of additional, even weakly basic ligands, the Cu+-Fe(CO)5 bond strength decreases what may contribute to the complex's instability in liquid SO2 or in the presence of [SbF6]−. These conclusions point at the key role of selection of proper anion and solvent in stabilization of these types of complexes. 相似文献
109.
A simple and efficient method for the highly stereoselective C-9 arylation and vinylation of Cinchona alkaloids was developed. Both 9S- and 9R-chloroquinine with PhMgBr yielded 9S-phenylquinine (X-ray structure). The reactions with various aryl and vinyl Grignard reagents resulted in the series of 9S-aryl and vinyl alkaloid derivatives. The stereochemical outcome was rationalized by coordination of the magnesium atom to the quinuclidine nitrogen, thus directing the nucleophilic attack at the C-9 stereogenic center. 相似文献
110.
Emilia Miszczyk Rafał Mazur Przemysław Morawiak Mateusz Mrukiewicz Wiktor Piecek Zbigniew Raszewski 《Liquid crystals》2018,45(11):1690-1698
There exists a problem in advanced numerically controlled automatic laser metrology. Reported study is related to minimising the system generating three or more coherent laser measuring beams. These rays, generated in a proper rangefinder, are necessary to determine the spatial coordinates and spatial orientation of the measured details. The simplest solution is to generate laser coherent light beams of wavelength λ = 0.6328 µm with a given light polarisation plane and then to direct them along three or more independent optical paths. To form these optical paths, a special refractive index matched liquid crystal cell (MLCC) might be applied. To ensure a stable laser operation during the measurement process, the back reflection of the laser beam from MLCC should not exceed 0.7%. The main task of this work is developing such a MLCC transducer. To reach the critical back reflection low enough, the MLCC is constructed as multilayer structure. MLCC operates in positive twisted nematic (TN) mode. Owing to the high-birefringence nematic liquid crystal mixture used and rather big cell gap, the elaborated low reflective MLCC (with R < 0.7%) works at TN mode above the sixth interference maximum of transmitting linearly polarised light. 相似文献