Výsledky vyhledávání - "Naz M. Aghatabay"

X-ray, tautomeric preference, vibrational spectra, and density functional studies on benzoxazole and benzoxazoline derivatives

Autor: Ahmet Altun, Naz M. Aghatabay, Serkan Dursun

Publikováno v: Vibrational Spectroscopy. 81:1-12

The solid-state X-ray diffraction, FT-IR, and FT-Raman measurements have been performed on bis(benzoxazole-2-ylthio)methane. Molecular structures and normal vibrations of bis(benzoxazole-2-ylthio)methane have been compared with those of its fragments

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c3f1e84b7ca3e2b87d4fb3a0c8ce18ce
https://doi.org/10.1016/j.vibspec.2015.09.001

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Synthesis, spectroscopic characterization and density functional studies of a bis-benzimidazole derivative and of its complexes with palladium(II) halides

Autor: Ahmet Altun, Naz M. Aghatabay, Mustafa Ulvi Gürbüz, Murat Turkyilmaz

Publikováno v: Comptes Rendus Chimie. 17:905-912

The 2,6-bis(benzimidazol-2′-ylthiomethyl)pyridine (L) ligand and its palladium(II) complexes [Pd(L)X]X (X = Cl, Br, and I) have been synthesized and characterized by spectroscopic data acquisition. The ligand (L) was prepared by conventional heatin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b5a4850091f1100c204c7a35232f82b3
https://doi.org/10.1016/j.crci.2013.10.016

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Synthesis, structural aspects, antimicrobial activity and ion transport investigation of five new [1+1] condensed cycloheterophane peptides

Autor: Mustafa Ulvi Gürbüz, Basaran Dulger, Ömer Zaim, Naz M. Aghatabay, Çağlar Baydar

Publikováno v: Journal of Inclusion Phenomena and Macrocyclic Chemistry. 78:151-159

Zaim, Omer/0000-0002-3472-5611; Dulger, Basaran/0000-0002-3184-2652; Dulger, Basaran/0000-0002-3184-2652; Gurbuz, Mustafa Ulvi/0000-0002-8684-5746 WOS: 000334496700015 Five novel [1+1] condensed cycloheterophane peptides were synthesized via reaction

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cd5e8b1a5a965416ef69b8374406bfe
https://doi.org/10.1007/s10847-012-0282-x

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X-ray, vibrational spectra and density functional studies on cynacure

Autor: Ahmet Altun, Naz M. Aghatabay

Publikováno v: Vibrational Spectroscopy. 64:68-77

The solid-state X-ray diffraction, FT-IR and FT-Raman measurements of cynacure have been performed. Optimized molecular structures and normal vibrations of cynacure and 2-(methylthio)aniline have been calculated in the gas phase at the B3LYP/6-311++G

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2ebf874b3c3dcea3a21743ffa967de78
https://doi.org/10.1016/j.vibspec.2012.11.001

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Synthesis, structural aspects, and antimicrobial activity investigation of novel macrocyclic amide-containing compounds

Autor: Murat Turkyilmaz, Basaran Dulger, S. Gündüz, Naz M. Aghatabay, A. Baş, H. R. F. Karabulut

Publikováno v: Chemistry of Heterocyclic Compounds. 48:936-942

Macrocyclic 16,76-dimethyl-1,7(2,4)-ditriazina-2,6,8,12-tetraaza-3,5,9,11-tetraoxocyclododecaphane, 16,86-dimethyl-1,8(2,4)-ditriazina-2,7,9,14-tetraaza-3,6,10,13-tetraoxocyclotetradecaphane, 16,96-dimethyl-1,9(2,4)-ditriazina-2,8,10,16-tetraaza-3,7,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9dd2e677d3faa20017fd4388ee0f6d67
https://doi.org/10.1007/s10593-012-1080-5

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Synthesis, FT-Raman, FT-IR, NMR spectroscopic characterization and antimicrobial activity of new mixed aza-oxo-thia macrocyclic compounds

Autor: Hüseyin Çevik, Basaran Dulger, Yaghub Mahmiani, Naz M. Aghatabay, Fahrettin Gücin

Publikováno v: Structural Chemistry. 19:833-842

Series of new mixed aza-oxo-thia macrocyclic ligands {2,6,12,16-tetraaza-1,7,11,17-tetraoxo-9,19-dithia-[(4′-methyl-5′,4,3′)(14′-methyl-15′,14,13′)]ditriazine}cyclocosane (L1); {2,6,13,17-teraaza-1,7,12,18-tetraoxo-9,10,20,21-tetrathia-[(

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0d2ac1aab0b20642c3be86c45aaa8cd5
https://doi.org/10.1007/s11224-008-9373-0

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FT-Raman, FT-IR, NMR structural characterization and antimicrobial activities of 1,6-bis(benzimidazol-2-yl)-3,4-dithiahexane ligand and its Hg(II) halide complexes

Autor: Mehmet Somer, Metin Tülü, Yaghub Mahmiani, Basaran Dulger, Naz M. Aghatabay

Publikováno v: Structural Chemistry. 19:71-80

1,6-Bis(benzimidaz-2-yl)-3,4-dithiahexane ligand (L) and its mercury halide complexes were prepared and characterised. The elemental analysis, molecular conductivity, FT-Raman, FT-IR (mid, far), 1H, 13C NMR and geometry optimization in MOPAC using MN

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::423d68b3e230626fe2050b2a87e198f6
https://doi.org/10.1007/s11224-007-9253-z

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FT-Raman, FT-IR and NMR spectra, vibrational assignments and density functional studies of 1,3-bis(benzimidazol-2-yl)-2-thiapropane ligand and its Zn(II) halide complexes

Autor: Durata Haciu, Metin Tülü, Naz M. Aghatabay, Mehmet Somer, Ayberk Yilmaz

Publikováno v: Structural Chemistry. 19:21-32

1,3-bis(benzimidazol-2-yl)-2-thiapropane (L) ligand and its zinc halide ZnX2 (X = Cl, Br, I) complexes have been synthesized. The compounds were characterized using the elemental analysis, molar conductivity, FT-Raman, FT-IR (mid i.r., far i.r.), 1H

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::59324a6644049f40109b4fbd16bb5c41
https://doi.org/10.1007/s11224-007-9238-y

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Tautomeric conversion, vibrational spectra, and density functional studies on peripheral sulfur derivatives of benzothiazole and benzothiazoline isomers

Autor: Ahmet Altun, Eziz Kuliyev, Naz M. Aghatabay

Publikováno v: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 152

The room temperature structural (tautomerism, dimerization, conformational preference, geometry parameters) and vibrational spectral (IR and Raman) analyses have been performed on benzothiazoline (benzothiazoline-2-thione, 3-methyl-benzothiazoline-2-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::824433874474ea4d218a01b780e42eb3
https://pubmed.ncbi.nlm.nih.gov/26210013

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