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    Öğe
    Spectroscopic studies and crystal structure of 3-[(2-morpholinoethylimino)methyl]benzene-1,2-diol
    (Springer/Plenum Publishers, 2008) Uenver, Hueseyin; Yıldız, Mustafa; Ocak, Nazan; Durlu, Tahsin Nuri
    Schiff base 3-[(2-morpholinoethylimino)methyl]benzene-1,2-diol has been synthesized from the reaction of 4-(2-aminoethyl)morpholine with 2,3-dihydroxybenzaldehyde. The title compound has been characterized by elemental analysis, IR, H-1-NMR, C-13-NMR and UV-visible techniques. The structure of the compound also has been examined crystallographically. For the compound exist as dominant form of enol-imines in both the solutions and solid state. The crystal structure has been solved by direct methods and refined by full-matrix least squares. The title compound crystallize in the monoclinic space group P2(1)/n with a = 12.085(1), b = 8.256(1), c = 13.650(1) angstrom, beta = 108.56(1)degrees, V = 1291.1(2) angstrom(3), D (x) = 1.288 g cm(-3), respectively (R-1 = 0.0336 and wR(2) = 0.0922 for 2117 reflections [I > 2 sigma(1)].
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    Öğe
    Spectroscopic studies, antimicrobial activities, and crystal structure of N-[2-hydroxy-1-naphthylidene]3,5-bis(trifluoromethyl)aniline
    (Springer/Plenum Publishers, 2006) Ünver, Hüseyin; Yıldız, Mustafa; Kiraz, Aşkın; İskeleli, Nazan Ocak; Erdönmez, Ahmet; Dülger, Başaran; Durlu, Tahsin Nuri
    A new Schiff base compound has been synthesized by the reaction of 2-hydroxy-1-naphthaldehyde with 3,5-bis(trifluoromethyl)aniline.The title compound was characterized by elemental analysis, IR, H-1 NMR, C-13 NMR, and UV-Visible techniques.Its UV-Vis spectra was examined in polar and nonpolar solvents and in acidic and basic media. The crystal structure of the compound showed the OH group to be ortho to the imine group. It crystallizes in the monoclinic space group P2(1) with a = 11.328(2), b = 6.125(1), c = 11.937(2) angstrom, V = 825.1(2) angstrom(3), D (x) = 1.543 g cm(-3) and Z = 2. An intramolecular O1- H center dot center dot center dot N1 [2.558(7) angstrom] hydrogen bond stabilizes the molecule. The compound has also been characterized by its antimicrobial activities. The ligand has been screened in vitro against the organisms Escherichia coli ATCC 11230, Staphylococcus aureus ATCC 6538, Klebsiella pneumoniae UC57, Micrococcus luteus La 2971, Proteus vulgaris ATCC 8427, Pseudomonas aeruginosa ATCC 27853, Mycobacterium smegmatis CCM 2067, Bacillus cereus ATCC 7064, and Listeria monocytogenes ATCC 15313, the yeast cultures Candida albicans ATCC 10231, Kluyveromyces fragilis NRRL 2415, Rhodotorula rubra DSM 70403, Debaryomyces hansenii DSM 70238, and Hanseniaspora guilliermondii DSM 3432.
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    Öğe
    Spectroscopic study and structure of (E)-2-[(2-chlorobenzylimino)methyl]methoxyphenol
    (Pergamon-Elsevier Science Ltd, 2009) Unver, Hueseyin; Yıldız, Mustafa; Ozay, Hava; Durlu, Tahsin Nuri
    (E)-2-[(2-Chlorobenzylimino)methyl]methoxyphenol has been synthesized from the reaction of 2-hydroxy-3-methoxy-1-benzaldehyde(o-vanillin) with 2-chlorobenzylamine. The title compound has been characterized by using elemental analysis, FT-IR, H-1 NMR, C-13 NMR and UV-vis spectroscopic techniques. The crystal structure of the title compound has also been examined cyrstallographically. It crystallizes in the orthorhombic space group Pbca with unit cell parameters: a = 7.208(1)angstrom, b = 13.726(2)angstrom, c= 27.858(4) angstrom, V= 2756.0(1) angstrom(3), D, = 1.18 g cm(-3) and Z= 8. The crystal structure was solved by direct methods and refined by full-matrix least squares to a find R=0.046 for 2773 observed reflections. (C) 2009 Elsevier B.V. All rights reserved.
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    Öğe
    Synthesis and spectroscopic properties of geminal-bis(tert-butylamino)cyclotriphosphazenes obtained by the reaction of Spiro and ansa phenoxycyclotriphosphazenes with the tert-butylamine and the crystal structure of 4,4?-bis(tert-butylamino)-2,6?,6?,10-tetrachloro-4?,4?,6?,6?-tetrahydrospyro[12H-dibenzo[d,g]- (1,3,2]dioxaphosphocin-6,2??5-[1,3,5,2,4,6]-triazaphosphorine]
    (Serbian Chemical Soc, 2011) Erdener, Digdem; Yıldız, Mustafa; Unver, Huseyin; Iskeleli, Nazan Ocak; Durlu, Tahsin Nuri
    The condensation reactions of partly substituted spiro and ansa phcnoxycyclotriphosphazenes 1 and 2 with tert-butylamine produce disubstituted geminal-bis(tert-butylamino)phenoxycyclotriphosphazene derivatives (3 and 4). The structures of these compounds were characterized by elemental analysis, and IR, H-1-, C-13-, P-31-NMR and mass spectroscopic techniques. Compound 3 was also examined by X-ray crystallography and found to be crystallized in the monoclinic space group P2(1)/n with the unit cell parameters: a = = 10.842(4), b = 9.375(5), c = 29.104(11) angstrom, beta = 99.25(3), V= 2920(2) angstrom(3), D-x = 1.404 g cm(-3).
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    Öğe
    Synthesis, spectroscopic studies and structure of 2-[(Benzo[d]thiazol-2- ylamino)methyl]phenol
    (Springer New York LLC, 2010) Yıldız, Mustafa; Özay, Hava; Ünver, Hüseyin; İskeleli, Nazan Ocak; Mehmet Zengin, D.; Durlu, Tahsin Nuri
    Schiff base (E)-2-[(benzo[d]thiazol-2-ylimino)methyl]phenol (1) has been synthesized from the reaction of 2-hydroxy-benzaldehyde with 2-aminobenzothiazole. The 2-[(benzo[d]thiazol-2-ylamino)methyl]phenol (2) was prepared reduction of the Schiff base 1 with sodium borohydride. The compounds 1 and 2 have been characterized by elemental analysis, FT-IR, 1 H-NMR, 13 C-NMR and UV-visible spectroscopic techniques. The structure of the compound 2 has also been examined crystallographically. The compound 2 crystallizes in the monoclinic space group P2/c. The unit cell parameters were found as a = 10.017(1), b = 11.725(1), c = 10.341(1) Å, V = 1208.1(1) Å 3 , D x = 1.409 g cm -3 and Z = 4. The crystal structure was solved by direct methods and refined by the full-matrix least squares method and found as R 1 = 0.0308 and wR 2 = 0.0818 for 2032 for the observed reflections [I > 2?(I)]. Graphical Abstract: Crystal and molecular structure of the compound 2-[(benzo[d]thiazol-2- ylamino)methyl]phenol have been studied in order to reveal the presence of either the enol-imine or keto-amine forms related with hydrogen bonding by using FT-IR, 1 H-NMR, 13 C-NMR, UV-visible spectroscopic and X-ray crystallographic techniques.[Figure not available: see fulltext.] © 2010 Springer Science+Business Media, LLC.
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    Öğe
    Synthesis, Spectroscopic Studies and Structure of 2-[(Benzo[d]thiazol-2-ylamino)methyl]phenol
    (Springer/Plenum Publishers, 2010) Yıldız, Mustafa; Ozay, Hava; Unver, Huseyin; Iskeleli, Nazan Ocak; Zengin, D. Mehmet; Durlu, Tahsin Nuri
    Schiff base (E)-2-[(benzo[d]thiazol-2-ylimino)methyl]phenol (1) has been synthesized from the reaction of 2-hydroxy-benzaldehyde with 2-aminobenzothiazole The 2-[(benzo[d]thiazol-2-ylamino)methyl]phenol (2) was prepared reduction of the Schiff base 1 with sodium borohydride The compounds 1 and 2 have been characterized by elemental analysis, FT-IR, H-1-NMR, C-13-NMR and UV-visible spectroscopic techniques The structure of the compound 2 has also been examined crystallographically The compound 2 crystallizes in the monoclinic space group P2/c The unit cell parameters were found as a = 10 017(1), b = 11 725(1), c = 10 341(1) angstrom, V = 1208 1(1) A(3), D-x = 1 409 g cm(-3) and Z = 4 The crystal structure was solved by direct methods and refined by the full-matrix least squares method and found as R-1 = 0 0308 and wR(2) = 0 0818 for 2032 for the observed reflections [1 > 2 sigma(1)]