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41.
Alraqa Shaya Y. Kaya Esra Nur Taşci Neşe Erbahar Dogan Durmuş Mahmut 《Journal of fluorescence》2022,32(5):1801-1813
Journal of Fluorescence - In this current study, the novel bis[4,5-(pyrene-2-yl)-3,6-(hexyloxy)] phthalonitrile (SPN) fluorophore has been successfully synthesized. Structural characterization of... 相似文献
42.
Ahmet Kilic Mahmut Ulusoy Mustafa Durgun Zeynep Tasci Ismail Yilmaz Bekir Cetinkaya 《应用有机金属化学》2010,24(6):446-453
Based on the a ligand BDPPZ [(9a,13a‐dihydro‐4,5,9,14‐tetraaza‐benzo[b]triphenylene‐11‐yl)‐phenyl‐methanone] (1) and its polypyridyl hetero‐ and homoleptic Ru(II) metal complexes, [Ru(bpy)2L](PF6)2 (2), [Ru(phen)2L](PF6)2 (3), [Ru(dafo)2L](PF6)2 (4), [Ru(dcbpy)2L](PF6)2 (5) and [RuL3](PF6)2 (6) (where, L = ligand, bpy = 2,2′‐bipyridine, phen = 1,10‐phenantroline, dafo = 4,5‐diazafluoren‐9‐one and dcbpy = 3,3′‐dicarboxy‐2,2′‐bipyridine), have been synthesized and characterized by elemental analysis, UV–vis, FT‐IR, 1H and 13C‐NMR spectra (for ligand), molar conductivity measurements and X‐ray powder techniques. The electrochemical parameters of the substituted ligand and its polypyridyl hetero‐ and homoleptic Ru(II) metal complexes are reported by cyclic voltammetry. UV–vis spectroscopy is used to compare the differences between the conjugated π systems in this ligand and its Ru(II) metal complexes. The polypyridyl hetero‐ and homoleptic Ru(II) metal complexes also tested as catalysts for the formation of cyclic organic carbonates from carbon dioxide and liquid epoxides which served as both reactant and solvent. The results showed that the [Ru(L)3](PF6)2 (6) complex is more efficient than the other Ru(II) complexes for the formation of cyclic organic carbonates from carbon dioxide. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
43.
Hasan Kocaokutgen Mahmut Gür Ibrahim Uar Sevil
zknal Orhan Büyükgüngr 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(2):o111-o113
The crystal structures of the title compounds, C17H15BrN2O2, (I), and C18H18N2O2, (II), determined at room temperature, have a trans configuration with respect to the diazene linkage, as found for other azo (diazene) derivatives. The aromatic mean planes are nearly coplanar, with a dihedral angle between these planes of 8.31 (2)° for (I) and 3.74 (2)° for (II). In both complexes, the mean plane of the ester group is nearly perpendicular to the aromatic ring planes. In both compounds, the crystal packing involves only π–π and π–ring interactions, which combine to stabilize the extended structure. 相似文献
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46.
Gnül Yenilmez ifti Mahmut Durmu Elif enkuytu Adem Kl 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2009,74(4):881-886
This study dealt with the reactions of hexachlorocyclotriphosphazatriene, N3P3Cl6 (trimer) (1) with phenolphthalein (2) to give the phenolphthalein bridged compounds 3, 4 and 5. The phenolphthalein bridged cyclotriphosphazatriene derivatives are reported for the first time. The new compounds (3–5) are characterized by elemental analysis, mass spectrometry, UV–vis, FT-IR, 1H, 31P NMR and fluorescence spectroscopy. The more bridged phenolphthalein groups show the higher intensity of the absorption bands in the UV–vis spectra. Fluorescence spectrum of compound 3 shows a small band in the lower spectral range, while the spectra of compounds 4 and 5 show more intense and a band in higher spectral range. 相似文献
47.
This is the first report on novel amphiphilic enantiomers as esters of alanine and serine with a partially fluorinated octyl chain (L-APFOE and L-SPFOE), which form intrinsic chiral nematic (N*) phases with water only and exhibit very high helical twisting powers (htps) compared to their hydrogenated counterparts, dodecylesters of L-alanine (L-ADDE) and L-serine (l-SDDE). They also exhibit a wider N* range than those known in the literature. Furthermore, the htps of the chiral dopants mandelic acid (MA) and hexahydromandelic acid (HHMA) in the racemic nematic phase of DL-SPFOE and DL-APFOE are remarkably higher than those in the hydrogenated counterparts. The tremendous increase in chirality (htps) of the same single chiral center is a new phenomenon in micellar N* phases and is attributed to a "pivot" effect of the fluoroalkyl chain. As a result, a "skewed micelle" model is proposed to explain why the htp value of L-APFOE is higher than that of L-SPFOE, and accordingly how the intermicellar chirality transfer (chiral induction) may be visualized. The simplicity of these binary mixtures and the enlargement in htp of the single chiral centers visualized as the "skewed micelle" model may provide a basis vital for future computer modeling of chiral lyotropics. 相似文献
48.
We consider geometric process (GP) when the distribution of the first occurrence time of an event is assumed to be Weibull. Explicit estimators of the parameters in GP are derived by using the method of modified maximum likelihood (MML) proposed by Tiku [24]. Asymptotic distributions and consistency properties of these estimators are obtained. We show that our estimators are more efficient than the widely used modified moment (MM) estimators via Monte Carlo simulation study. Further, two real life examples are given at the end of the paper. 相似文献
49.
This paper considers a multiple-supplier, single manufacturer assembly supply chain where the suppliers produce components of a short life-cycle product which is assembled by the manufacturer. In this single-period problem the suppliers determine their production quantities and the manufacturer chooses the retail price. We assume that the manufacturer faces a random price-dependent demand in either additive or multiplicative form. For each case, we analyze both simultaneous-move and leader–follower games to respectively determine the Nash and Stackelberg equilibria, and find the globally-optimal solution that maximizes the system-wide expected profit. Then, we introduce appropriate buy-back and lost-sales cost-sharing contracts to coordinate this assembly supply chain, so that when all the suppliers and the manufacturer adopt their equilibrium solutions, the system-wide expected profit is maximized. 相似文献
50.
A complete set of platinum(II) solketal substituted phthalocyanines has been synthesized and characterized. To evaluate their potential as Type II photosensitizers for photodynamic therapy, comparative studies of their photophysical and photochemical properties with analogous zinc(II) series have been achieved: electronic absorption, fluorescence quantum yields, lifetimes, and fluorescence quenching by benzoquinone, as well as singlet oxygen generation and photodegradation. It appears that platinum(II) phthalocyanines are worth being used as Type II photosensitizers, as they exhibit good singlet oxygen generation and appropriate photodegradation. 相似文献