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191.
Leyla Bitiş Sevda Süzgeç Ulaş Sözer Hasan Özçelik Josef Zapp Alexandra K. Kiemer Filiz Meriçli Ali H. Meriçli 《Helvetica chimica acta》2007,90(11):2217-2221
From the aerial parts of Delphinium buschianum Grossh ., collected in Turkey, a new diterpenoid alkaloid 1 , named budelphine, was isolated along with the known diterpenoid alkaloids karakoline ( 2 ), 18‐hydroxy‐14‐O‐methylgadesine ( 3 ), delsoline ( 4 ), lapaconidine ( 5 ), columbianine ( 6 ), 14‐benzoylneoline ( 7 ), and hetisine ( 9 ). The structure of 1 was established on the basis of 1H‐, 13C‐, DEPT, 1H,1H‐COSY, NOESY, HSQC, and HMBC NMR studies. 相似文献
192.
193.
194.
Y. D. Kurt G. S. Pozan İ. Kızılcıklı B. Ülküseven 《Russian Journal of Coordination Chemistry》2007,33(11):844-849
Mixed ligand complexes of dioxomolybdenum(VI) with 2-hydroxybenzaldehyde 4-phenyl-S-methylthiosemicarbazone (H2L) were prepared with the formula [MoO2(L)D] (D = H2O, methyl, n-butyl, and n-undecyl alcohol, DMF, DMSO, pyridine, 4-picoline, and 3,5-lutidine). The compounds were characterized by elemental
analysis, IR and 1H NMR spectroscopy. The thermal decomposition of the compounds were investigated by using TGA, DTG, and DTA methods in air,
and the thermal behavior depending on the second ligand molecule was discussed. A single crystal of the DMF coordinated complex
was studied by X-ray diffractometry.
The text was submitted by the authors in English. 相似文献
195.
A new (E,E)-dioxime, (6Z,7Z)-15,16-dihydro-14H-dibenzo[b,h][1,10,4, 7]dithiadiazacyclotride-cine-6,7(5H,8H)-dionedioxime (H
2
L) has been synthesized by reacting cyanogen-di-N-oxide (2) with 2,2′-[propane-1,3-diylbis(thio)]dianiline (1). Mononuclear complexes (4) and (5) of this ligand have been synthesized by reacting the vic-dioxime (H2L) with NiCl2 · 6H2O and CoCl2 · 6H2O, respectively. The BF
2
+
capped Ni(II) and Co(III) complexes (6) and (7) of the dioxime have been synthesized from (4) and (5). The new compounds were characterized by a combination of elemental analysis, 1H- and 13C-n.m.r, i.r. and m.s. spectral data. 相似文献
196.
The stoichiometry and stability constant of metal complexes with 4-(3-methoxy-salicylideneamino)-5-hydroxynaphthalene-2,7-disulfonic
acid monosodium salt (H2L) and 4-(3-methoxysalicylideneamino)-5-hydroxy-6-(2,5-dichlorophenylazo)-2,7-naphthalene disulfonic acid monosodium salt
(H2L1) were studied by potentiometric titration. The stability constants of H2L and H2L1 Schiff bases have been investigated by potentiometric titration and u.v.–vis spectroscopy in aqueous media. The dissociation
constants of the ligand and the stability constants of the metal complexes were calculated pH-metrically at 25 °C and 0.1 m KCl ionic strength. The dissociation constants for H2L were obtained as 3.007, 7.620 and 9.564 and for H2L1, 4.000, 6.525, 9.473 and 10.423, respectively. The complexes were found to have the formulae [M(L)2] for M = Co(II), Ni(II), Zn(II) and Cu(II). The stability of the complexes follows the sequence: Zn(II) < Co(II) < Cu(II)
< Ni(II). The high stability of H2L1 towards Cu(II) and Ni(II) over the other ions is remarkable, in particular over Cu(II), and may be of technological interest.
Concentration distribution diagram of various species formed in solution was evaluated for ligands and complexes. The formation
of the hydrogen bonds may cause this increased stability of ligands. The pH-metric data were used to find the stoichiometry,
deprotonation and stability constants via the SUPERQUAD computer program. 相似文献
197.
E. F. Keskenler S. Doğan B. Diyarbakır S. Duman B. Gürbulak 《Journal of Sol-Gel Science and Technology》2011,60(1):66-70
ZnO thin films were deposited onto glass subsrates by a Sol-gel spin coating method. The structural and optical properties
of ZnO thin films were investigated. The molar ratios of the zinc acetate dihydrate to Monoethanolamine were maintained 1:1.
The as-grown film was sintered 250 °C for 10 min, then annealed in air at 500 °C for 30 min. The XRD results indicate that
ZnO films were strongly oriented to the c-axis of the hexagonal nature. Absorption measurements were carried out as a function
of temperature with 10 K steps in the range 10–320 K. The band gap energy was measured 3.275 and 3.267 eV for 0.5 and 1.0
molarity (M) ZnO thin films at 300 K. The steepness parameters were observed between 10 and 320 K and their extrapolations
converged at (E0, α0) = 3.65 eV, 172,819 cm−1 and 3.70 eV, 653,436 cm−1 for 0.5 and 1.0 M ZnO thin films, respectively. 相似文献
198.
O. O. Soldatkin I. S. Kucherenko M. K. Shelyakina E. Soy K. Kirdeciler S. Öztürk N. Jaffrezic‐Renault B. Akata S. V. Dzyadevych A. P. Soldatkin 《Electroanalysis》2013,25(2):468-474
Different modifications of the zeolites Na+‐Beta and LTA were applied for improving the working characteristics of a urea biosensor. The bioselective membrane of the biosensor was based on urease and different zeolites co‐immobilized with bovine serum albumin on the surface of a pH‐FET. It was shown that the biosensors modified with the zeolites H+‐Beta30 and H+‐Beta50 are characterized by increased sensitivity to urea. The influence of the zeolite concentration on the sensitivity of the biosensors was studied. The optimal concentration of the zeolites H+‐Beta30 and H+‐Beta50 in the bioselective membrane was 15 %. Different variants of co‐immobilization of urease and zeolite H+‐Beta30 were studied and the optimal method was selected. Thus, a general conclusion is that the urea biosensor sensitivity can be improved using zeolite H+‐Beta30 for urease immobilization in the bioselective membrane. 相似文献
199.
Thorsteinn Loftsson Ína B. Össurardóttir Thorsteinn Thorsteinsson Matt Duan Már Másson 《Journal of inclusion phenomena and macrocyclic chemistry》2005,52(1-2):109-117
The natural β-cyclodextrin (βCD) and its complexes have limited solubility in aqueous solutions. This low aqueous solubility, as well as low aqueous solubility of the guest molecule (i.e. triclosan or triclocarban (TCC)), can result in low complexation efficiency (CE). The purpose of this study was to enhance the apparent intrinsic solubility (S
0) of the guest molecule and its βCD complexes through ionization and addition of auxiliary compounds such as polymers, amino acids and metal ions. Both triclosan (pK
a
7.9) and TCC (pK
a
12.7) are weak acids. Addition of ethanol to the complexation medium enhanced S
0 of both triclosan and TCC but at the same time ethanol lowered the stability constant (K
c
) of their βCD complexes resulting in overall lowering of CE. Addition of small amount of water-soluble polymers enhanced the βCD solubilization of both guests, and addition lysine enhanced the solubilization of TCC. Ionization of triclosan resulted in significant enhancement of CE and enhanced triclosan release from tablets containing triclosan/βCD complex. The effect of ionization was not as pronounced in the case of TCC.This revised version was published online in July 2005 with a corrected issue number. 相似文献
200.
U. Avcıbaşı H. Demiroğlu P. Ünak F. Z. B. Müftüler Ç. A. İçhedef F. G. Gümüşer 《Journal of Radioanalytical and Nuclear Chemistry》2010,285(2):207-214
Bleomycins (BLMs; BLM, A2, and B2) were labeled with 131I and radiopharmaceutical potentials were investigated using animal models in this study. Quality control procedures were
carried out using thin layer radiochromatography (TLRC), high performance liquid chromatography (HPLC), and liquid chromatography
(LC/MS/MS). Labeling yields of radiolabeled BLMs were found to be 90, 68, and 71%, respectively. HPLC chromatograms were taken
for BLM and cold iodinated BLM (127I-BLM). Five peaks were detected for BLM and three peaks for 127I-BLM in the HPLC studies. Two peaks belong to isomers of BLM. The isomers of BLM were purified with using HPLC. Biological
activity of BLM was determined on male Albino Wistar rats by biodistribution and scintigraphic studies were performed for
BLMs by using New Zelland rabbits. The biodistribution results of 131I-BLM showed high uptake in the stomach, the bladder, the prostate, the testicle, and the spinal cord in rats. Scintigraphic
results on rabbits agrees with that of biodistributional studies on rats. The scintigraphy of radiolabeled isomers (131I-A2 and 131I-B2) are similiarly found with that of 131I-BLM. 相似文献