Yazar "Dagci, Erdogan" seçeneğine göre listele

Listeleniyor 1 - 4 / 4
  • [ X ]
    Öğe
    N,N'-Bis-(2,5-dimethyl-3-oxo-1-phenyl-2,3-dihydro-1H-pyrazol-4-yl)phthalamide
    (Mdpi, 2012) Aydin, Fatma; Dagci, Erdogan
    The title compound, N,N'-bis-(2,5-dimethyl-3-oxo-1-phenyl-2,3-dihydro-1H-pyrazol-4-yl)phthalamide has been synthesized by reactions of o-phthaloyl chloride with 4-amino-2,5-dimethyl-1-phenyl-3-oxo-1H-pyrazolone in acetonitrile. The structure of the new compound was characterized by FT-IR, H-1 NMR, C-13 NMR and mass spectroscopic techniques. Physical parameters of the compound such as melting point, solubility,lambda(max) were examined.
  • [ X ]
    Öğe
    N,N?-Bis-(4-nitrophenylcarbamothioyl)phthalamide
    (Mdpi, 2013) Aydin, Fatma; Dagci, Erdogan
    A novel colorimetric receptor linked to two nitrophenylurea groups was synthesized in good yields, characterized and their chromogenic properties investigated towards various anions (F-, Cl-, Br-, I-, OH-, AcO-, H2PO4- and CN-) by UV-Vis techniques. The receptor, effectively and selectively, recognized and distinguished the biologically important F- from other anions such as Cl-, Br-, I- etc. in DMSO. This selectivity could be easily observed by the naked eye, indicating that receptor is potential colorimetric sensor for fluoride ion.
  • [ X ]
    Öğe
    N-[(2,5-Dimethyl-3-oxo-1-phenyl-2,3-dihydro-1H-pyrazol-4-yl)carbamothioyl]isonicotinamide
    (Mdpi, 2010) Aydin, Fatma; Dagci, Erdogan
    A new heterocyclic compound, N-[(2,5-dimethyl-3-oxo-1-phenyl-2,3-dihydro-1H-pyrazol-4-yl)carbamothioyl]isonicotinamide, was synthesized from isonicotinoyl isothiocyanate and 4-aminoantipyrine in acetonitrile solution. The title compound was characterized by FT-IR, H-1 NMR, C-13 NMR and MS spectroscopic methods. Physical parameters of the compound were examinated.
  • [ X ]
    Öğe
    Synthesis of New N-Benzoyl-S-alkyl/aryl-dithiocarbamates
    (Asian Journal Of Chemistry, 2010) Aydin, Fatma; Aykac, Dogan; Dagci, Erdogan
    New N-benzoyl-S-alky/aryldithiocarbamates were synthesized in moderate to good yields by the reactions of benzoyl isothiocyanate with substituted aryl- and akylthiols.