Shadia Elsayed | Damietta University (original) (raw)
Papers by Shadia Elsayed
Bioinorganic chemistry and applications, 2010
New complexes of dioxovanadium(V), zinc(II), ruthenium(II), palladium(II), and platinum(II) with ... more New complexes of dioxovanadium(V), zinc(II), ruthenium(II), palladium(II), and platinum(II) with 6-methylpyridine-2-carbaldehyde-N(4)-ethylthiosemicarbazone (HmpETSC) have been synthesized. The composition of these complexes is discussed on the basis of elemental analyses, IR, Raman, NMR ((1)H, (13)C, and (31)P), and electronic spectral data. The X-ray crystal structures of [VO(2)(mpETSC)] and [Pt(mpETSC)Cl] are also reported. The HmpETSC and its [Zn(HmpETSC)Cl(2)] and [Pd(mpETSC)Cl] complexes exhibit antineoplastic activity against colon cancer human cell lines (HCT 116).
ISRN Inorganic Chemistry, 2014
The new oxovanadium(V) complex, [VO(acac)(dametsc)] (1) (acac = acetylacetonate (-1), H 2 dametsc... more The new oxovanadium(V) complex, [VO(acac)(dametsc)] (1) (acac = acetylacetonate (-1), H 2 dametsc = diacetylmonoxime-4ethylthiosemicarbazone), has been prepared and characterized by studying its physicochemical properties. The X-ray crystal structure of the complex (1) has been determined and showed the presence of vanadium(V) atom in a unique heptacoordination state with distorted pentagonal bipyramidal geometry. The oximato ligand in the pentagonal plane is bonded to the central vanadium atom in dihapto ( 2 = N,O) manner with the formation of three membered ring, while the other three coordination sites in the plane are occupied by hydrazinic imine nitrogen, thiolate sulfur, and one of the acac oxygen atoms. The axial position sites are defined by the other acac oxygen and the trans oxo-atom. The supramolecular structure of the complex is exclusively constructed by intermolecular interactions, N-H⋅ ⋅ ⋅ O and C-H⋅ ⋅ ⋅ O.
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2014
New cis-dioxomolybdenum(VI) and oxovanadium(IV) complexes of the Schiff base, derived from S-meth... more New cis-dioxomolybdenum(VI) and oxovanadium(IV) complexes of the Schiff base, derived from S-methyl dithiocarbazate and 2,3-dihydroxybenzaldehyde (H2dhsm), have been synthesized. The complexes of the type cis-[MoO2(dhsm)] (1a), cis-[MoO2(dhsm)(D)] (1b-1d) [D=neutral monodentate ligand; EtOH, pyridine (py) or imidazole (imz)], [VO(dhsm)(NN)] (2a, 2b) [NN=2,2'-bipyridine (bipy) or 1,10-phenanthroline (phen)] and [VO(dhsm)] (2c) have been isolated, characterized by (1)H NMR, IR, UV-Vis and EPR spectral studies and investigated by cyclic voltammetry. The X-ray crystal structure of cis-[MoO2(dhsm)(EtOH)] (1b) has been determined and shows that the complex has a distorted octahedral geometry in which the H2dhsm behaves as a dianionic ONS tridentate ligand coordinating via phenoxide oxygen, hydrazinic nitrogen and thiolate sulfur. The oxomolybdenum(IV) complex [MoO(dhsm)] (1e) has obtained from dioxomolybdenum(VI) complex (1b) by oxo abstraction with PPh3. The reactivity of the complexes toward catalytic oxidation of alcohols in the presence of H2O2 and t-BuOOH as co-oxidants under solvent free conditions is reported.
Journal of Molecular Structure, 2013
This article appeared in a journal published by Elsevier. The attached copy is furnished to the a... more This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research and education use, including for instruction at the authors institution and sharing with colleagues.
Inorganica Chimica Acta, 2010
a b s t r a c t The syntheses of five new complexes of the 2-formylpyridinethiosemicarbazone liga... more a b s t r a c t The syntheses of five new complexes of the 2-formylpyridinethiosemicarbazone ligand (HFpyTSC) with Pd(II) and Rh(III) ions are described, viz., [Pd(FpyTSC)(PPh 3 )]PF 6 , [Pd(FpyTSC)(SCN)], [Pd(FpyTSC)Br], [Pd(HFpyTSC) 2 ]Br 2 and [Rh(FpyTSC)(PPh 3 ) 2 Cl]ClO 4 . The formulation of the complexes is discussed in terms of their elemental analyses and IR, Raman, NMR ( 1 H, 13 C and 31 P), mass and electronic spectra. The X-ray crystal structures of [Pd(FpyTSC)(PPh 3 )]PF 6 and [Pd(FpyTSC)(SCN)] show that the HFpyTSC ligand coordinates to the central Pd(II) ion in a planar conformation through the pyridyl nitrogen, the azomethine nitrogen and the deprotonated thiol sulphur atom. Thus, HFpyTSC is a versatile ligand that usually acts as a mononegative tridentate ligand bonding through N py , N C@N and C-S À while, in the case of [Pd(HFpyTSC) 2 ]Br 2 , it behaves as a neutral bidentate ligand via N C@N and C@S.
Bioinorganic Chemistry and Applications, 2010
New complexes of dioxovanadium(V), zinc(II), ruthenium(II), palladium(II), and platinum(II) with ... more New complexes of dioxovanadium(V), zinc(II), ruthenium(II), palladium(II), and platinum(II) with 6-methylpyridine-2carbaldehyde-N(4)-ethylthiosemicarbazone (HmpETSC) have been synthesized. The composition of these complexes is discussed on the basis of elemental analyses, IR, Raman, NMR ( 1 H, 13 C, and 31 P), and electronic spectral data. The X-ray crystal structures of [VO 2 (mpETSC)] and [Pt(mpETSC)Cl] are also reported. The HmpETSC and its [Zn(HmpETSC)Cl 2 ] and [Pd(mpETSC)Cl] complexes exhibit antineoplastic activity against colon cancer human cell lines (HCT 116).
Bioinorganic chemistry and applications, 2010
New complexes of dioxovanadium(V), zinc(II), ruthenium(II), palladium(II), and platinum(II) with ... more New complexes of dioxovanadium(V), zinc(II), ruthenium(II), palladium(II), and platinum(II) with 6-methylpyridine-2-carbaldehyde-N(4)-ethylthiosemicarbazone (HmpETSC) have been synthesized. The composition of these complexes is discussed on the basis of elemental analyses, IR, Raman, NMR ((1)H, (13)C, and (31)P), and electronic spectral data. The X-ray crystal structures of [VO(2)(mpETSC)] and [Pt(mpETSC)Cl] are also reported. The HmpETSC and its [Zn(HmpETSC)Cl(2)] and [Pd(mpETSC)Cl] complexes exhibit antineoplastic activity against colon cancer human cell lines (HCT 116).
ISRN Inorganic Chemistry, 2014
The new oxovanadium(V) complex, [VO(acac)(dametsc)] (1) (acac = acetylacetonate (-1), H 2 dametsc... more The new oxovanadium(V) complex, [VO(acac)(dametsc)] (1) (acac = acetylacetonate (-1), H 2 dametsc = diacetylmonoxime-4ethylthiosemicarbazone), has been prepared and characterized by studying its physicochemical properties. The X-ray crystal structure of the complex (1) has been determined and showed the presence of vanadium(V) atom in a unique heptacoordination state with distorted pentagonal bipyramidal geometry. The oximato ligand in the pentagonal plane is bonded to the central vanadium atom in dihapto ( 2 = N,O) manner with the formation of three membered ring, while the other three coordination sites in the plane are occupied by hydrazinic imine nitrogen, thiolate sulfur, and one of the acac oxygen atoms. The axial position sites are defined by the other acac oxygen and the trans oxo-atom. The supramolecular structure of the complex is exclusively constructed by intermolecular interactions, N-H⋅ ⋅ ⋅ O and C-H⋅ ⋅ ⋅ O.
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2014
New cis-dioxomolybdenum(VI) and oxovanadium(IV) complexes of the Schiff base, derived from S-meth... more New cis-dioxomolybdenum(VI) and oxovanadium(IV) complexes of the Schiff base, derived from S-methyl dithiocarbazate and 2,3-dihydroxybenzaldehyde (H2dhsm), have been synthesized. The complexes of the type cis-[MoO2(dhsm)] (1a), cis-[MoO2(dhsm)(D)] (1b-1d) [D=neutral monodentate ligand; EtOH, pyridine (py) or imidazole (imz)], [VO(dhsm)(NN)] (2a, 2b) [NN=2,2'-bipyridine (bipy) or 1,10-phenanthroline (phen)] and [VO(dhsm)] (2c) have been isolated, characterized by (1)H NMR, IR, UV-Vis and EPR spectral studies and investigated by cyclic voltammetry. The X-ray crystal structure of cis-[MoO2(dhsm)(EtOH)] (1b) has been determined and shows that the complex has a distorted octahedral geometry in which the H2dhsm behaves as a dianionic ONS tridentate ligand coordinating via phenoxide oxygen, hydrazinic nitrogen and thiolate sulfur. The oxomolybdenum(IV) complex [MoO(dhsm)] (1e) has obtained from dioxomolybdenum(VI) complex (1b) by oxo abstraction with PPh3. The reactivity of the complexes toward catalytic oxidation of alcohols in the presence of H2O2 and t-BuOOH as co-oxidants under solvent free conditions is reported.
Journal of Molecular Structure, 2013
This article appeared in a journal published by Elsevier. The attached copy is furnished to the a... more This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research and education use, including for instruction at the authors institution and sharing with colleagues.
Inorganica Chimica Acta, 2010
a b s t r a c t The syntheses of five new complexes of the 2-formylpyridinethiosemicarbazone liga... more a b s t r a c t The syntheses of five new complexes of the 2-formylpyridinethiosemicarbazone ligand (HFpyTSC) with Pd(II) and Rh(III) ions are described, viz., [Pd(FpyTSC)(PPh 3 )]PF 6 , [Pd(FpyTSC)(SCN)], [Pd(FpyTSC)Br], [Pd(HFpyTSC) 2 ]Br 2 and [Rh(FpyTSC)(PPh 3 ) 2 Cl]ClO 4 . The formulation of the complexes is discussed in terms of their elemental analyses and IR, Raman, NMR ( 1 H, 13 C and 31 P), mass and electronic spectra. The X-ray crystal structures of [Pd(FpyTSC)(PPh 3 )]PF 6 and [Pd(FpyTSC)(SCN)] show that the HFpyTSC ligand coordinates to the central Pd(II) ion in a planar conformation through the pyridyl nitrogen, the azomethine nitrogen and the deprotonated thiol sulphur atom. Thus, HFpyTSC is a versatile ligand that usually acts as a mononegative tridentate ligand bonding through N py , N C@N and C-S À while, in the case of [Pd(HFpyTSC) 2 ]Br 2 , it behaves as a neutral bidentate ligand via N C@N and C@S.
Bioinorganic Chemistry and Applications, 2010
New complexes of dioxovanadium(V), zinc(II), ruthenium(II), palladium(II), and platinum(II) with ... more New complexes of dioxovanadium(V), zinc(II), ruthenium(II), palladium(II), and platinum(II) with 6-methylpyridine-2carbaldehyde-N(4)-ethylthiosemicarbazone (HmpETSC) have been synthesized. The composition of these complexes is discussed on the basis of elemental analyses, IR, Raman, NMR ( 1 H, 13 C, and 31 P), and electronic spectral data. The X-ray crystal structures of [VO 2 (mpETSC)] and [Pt(mpETSC)Cl] are also reported. The HmpETSC and its [Zn(HmpETSC)Cl 2 ] and [Pd(mpETSC)Cl] complexes exhibit antineoplastic activity against colon cancer human cell lines (HCT 116).