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81.
Hasan Tanak İlhan Özer İlhan Necmi Dege Nazenin Akın Emin Sarıpınar 《Crystallography Reports》2017,62(7):1078-1082
Crystal structure of the title compound C22H19N3O is determined by single crystal X-ray diffraction (sp. gr. P21/c, Z = 4). The molecule as a whole, is not planar: phenyl cycles are rotated relative to the plane of pyrazole ring. N?H···N intramolecular hydrogen bond forms five-membered ring fused to pyrazole ring. There are also intramolecular C?H···O and C?H···π interactions. Intermolecular C?H···O hydrogen bond links the molecules into a C(7) chain along the a axis. The crystal structure is stabilized also by C–H···π and π···π intermolecular hydrogen bonds. 相似文献
82.
Arif Sanli Ozlem Celebi Mehmet Eken Alev Oktay Sedat Aydin Emin Ayduran 《Journal of voice》2008,22(2):238-244
SUMMARY: Visualization of enlarged laryngeal lesions is the most important factor in choosing a surgical technique, especially for partial surgery. For this reason standard microlaryngoscopy, a computed tomography (CT) scan of the larynx, and 30 degrees telescopic microlaryngoscopy were compared during evaluation of the laryngeal ventricul and sub-glottic area. The histopatholgoical findings of the specimens collected under each modality were simultaneously compared. Comparison of the histopathological findings, which corresponded to inspection with the 30 degrees telescopic method, was more significant than with the use of standard microlaryngoscopy or the CT scan. The aim of the current study therefore was to determine the importance of the 30 degrees telescopic microlaryngoscopic method for the evaluation of the laryngeal ventricle and subglottic area. 相似文献
83.
In this paper, we analyze the problem of constructing a surface pencil from a given spacelie (timelike) line of curvature. Using the Frenet frame of the given line of curvature in Minkowski 3-space, we express the surface pencil as a linear combination of this frame and derive the necessary and sufficient conditions for the coefficients to satisfy the line of curvature requirement. We illustrate this method by presenting some examples. 相似文献
84.
Time-resolved photoluminescence studies reveal distinct differences between the recombination processes in a chalcogenide glass and in its crystalline counterpart. Here the three luminescence bands of a-As2S3 are interpreted in terms of the recombination of an excition, a self-trapped exciton and a pair of electron- and hole-like small polarons. The two luminescence bands observed in the crystal are attributed to the recombination of two types of excitons composed respectively of a hole bound to a self-trapped electron, and a hole which is induced to self-trap in the presence of a self-trapped electron. 相似文献
85.
Yunus Akcamur Behzat Altural Emin Saripinar Gert Kollenz Oliver Kappe Karl Peters Eva-Maria Peters Hans-Georg Von Schnering 《Journal of heterocyclic chemistry》1988,25(5):1419-1422
The furan-2,3-dione 1 and the thiosemicarbazones 2 combine with loss of carbon dioxide and water yielding the 1-methylenaminopyrimidine-2-thione derivatives 3 in moderate yields (30–60%). Their molecular skeleton is confirmed with aid of an X-ray structure determination of 3c . Hydrolysis of 3 leads to the 1-aminopyrimidine-2-thione 5 . 相似文献
86.
Flotation is one of the plausible methods for recovering borax fines discharged as fine waste to the tailings dam in the Kirka borax processing plant. A literature review dealing with the flotation behavior of boron minerals reveals that clay minerals in the boron ores coat boron minerals and thus deteriorate the quality of boron concentrates produced by direct flotation. The main objective of this study is therefore to recover borax fines from the tailings of the concentrator by reverse flotation. A three-level-factor experimental design was used to determine the main and interaction effects of variables selected on the metallurgical performance of reverse flotation. An analysis of variance for experimental results indicates that interaction effects of the variables for concentrate quality and recovery of B2O3 is nonsignificant and the most important variable for grade of concentrate and recovery is the collector dosage. It is shown that a concentrate assaying 11.25% B2O3 with 89.90% B2O3 recovery could be produced by means of single-stage (rougher) reverse flotation. Additionally, in order to produce a sufficient-quality concentrate, a multistage reverse flotation scheme involving rougher, scavenger, and two cleaners was devised. A final concentrate containing 23.47% B2O3 with 81.78% B2O3 recovery was obtained from these tests. The reverse flotation method can be thus considered as an important option for the beneficiation of borax fines. 相似文献
87.
Emin Karapinar Emine Özcan 《Journal of inclusion phenomena and macrocyclic chemistry》2003,47(1-2):59-63
N'-[4'-benzo(15-crown-5)]-4-tolylaminoglyoxime (H2L1),the sodium chloride salt of H2L1 (H2L1...NaCl),N'-[4'-benzo(15-crown-5)]-4-chlorophenylaminoglyoxime(H2L2) and the sodium chloride salt of H2L2 (H2L2...NaCl)have been prepared from p-chlorophenylchloroglyoxime,p-tolylchloroglyoxime, 4'-aminobenzo[15-crown-5] and sodiumbicarbonate or sodium bicarbonate and sodium chloride. Nickel (II),cobalt (II) and copper (II) complexes of H2L and H2L...NaClhave a metal-ligand ratio of 1 : 2 and the ligand coordinatesthrough the two N atoms, as do most of the vic-dioximes. Their IR spectra and elemental analyses are given, together with1H NMR spectra of the ligands. 相似文献
88.
Four unsymmetrical vic-dioximes: [L1H2] N-(4-butylphenyl)amino-amphi-glyoxime, [L2H2] N-(4-butylphenyl)amino-anti-glyoxime, [L3H2] N-(4-phenylazophenyl)amino-amphi-glyoxime and [L4H2] N-(4-phenylazophenyl)amino-anti-glyoxime have been prepared from amphi-chloroglyoxime, anti-chloroglyoxime, 4-butylaniline and 4-(phenylazo)aniline respectively. The complexes of these vic-dioximes with NiII, CoII, CuII and CdII ions have been investigated. All are insoluble in common solvents. Their i.r. spectra and elemental analyses are given, together with mass and 1H-n.m.r. spectra of the ligands. 相似文献
89.
Gourdon D Lin Q Oroudjev E Hansma H Golan Y Arad S Israelachvili J 《Langmuir : the ACS journal of surfaces and colloids》2008,24(4):1534-1540
Using a surface forces apparatus, we have investigated the adhesive and lubrication forces of mica surfaces separated by a molecularly thin, subnanometer film of a high-molecular-weight (2.3 MDa) anionic polysaccharide from the algae Porphyridium sp. adsorbed from aqueous solution. The adhesion and friction forces of the confined biopolymer were monitored as a function of time, shearing distance, and driving velocity under a large range of compressive loads (pressures). Although the thickness of the dilute polysaccharide was <1 nm, the friction was low (coefficient of friction = 0.015), and no wear was ever observed even at a pressure of 110 atm over 3 decades of velocity, so long as the shearing distances were less than twice the contact diameter. Atomic force microscopy in solution shows that the biopolymer is able to adsorb to the mica surface but remains mobile and easily dragged upon shearing. The adhesion (adsorption) of this polysaccharide even to negatively charged surfaces, its stable low friction, its robustness (high-load carrying capacity and good wear protection), and the weak (logarithmic) dependence of the friction force on the sliding velocity make this class of polyelectrolytes excellent candidates for use in water-based lubricant fluids and as potential additives to synovial fluid in joints and other biolubricating fluids. The physical reasons for the remarkable tribological properties of the ultrathin polysaccharide monolayer are discussed and appear to be quite different from those of other polyelectrolytes and proteins that act as thick "polymer brush" layers. 相似文献
90.
Schmittel M Steffen JP Rodríguez D Engelen B Neumann E Cinar ME 《The Journal of organic chemistry》2008,73(8):3005-3016
Mechanistic details of the thermal C2-C6 cyclization of enyne-carbodiimides are investigated. A variety of product and kinetic studies on solvent and substituent effects open the way for a deeper mechanistic understanding. Nonlinear Hammett correlations suggest that a change of mechanism takes place: the thermal C2-C6 cyclization of enyne-carbodiimides with electron-withdrawing substituents may be best described as a coarctate cyclization to a carbene and with electron-donating substituents as a polar cyclization to a carbene with strong zwitterionic character. Theoretical investigations had originally suggested a diradical intermediate. DFT computations and NBO analysis for the parent diazafulvenediyl are in agreement with a carbene intermediate. While any intermolecular trapping of the intermediate failed, the formation of the C-H insertion product 19 strongly supports the carbene hypothesis. 相似文献