ORCID Profile
0000-0002-3386-2737
Current Organisation
RMIT University
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Publisher: Elsevier BV
Date: 11-2013
Publisher: Elsevier BV
Date: 12-2014
Publisher: Elsevier BV
Date: 11-2011
Publisher: Elsevier BV
Date: 10-2016
Publisher: Informa UK Limited
Date: 06-01-2015
Publisher: CSIRO Publishing
Date: 2020
DOI: 10.1071/CH19326
Abstract: The preference for incorporation of molybdenum over tungsten into specific sites of a family of yttrium-arsenotungstates with amino acid ligands prompted exploration of the incorporation of other metals, affording three new vanadium-containing (V/W and V/Mo/W) analogues: K2(GlyH)10[As4(V2W2)W44Y4O160(Gly)8(H2O)12]·11Gly (1), (MBAH)9(L-NleH)3[As4(V2W2)W44Y4O160(L-Nle)8(H2O)12] (2), and (MBAH)9(L-NleH)3[As4(V2W2)Mo2W42Y4O160(L-Nle)8(H2O)12] (3) (Gly=glycine and L-Nle=l-norleucine, MBAH=4-methylbenzylammonium). These hybrid polyoxometalates all possess a tetrametallic oxo-bridged {VIV2WVI2} central core surrounded by an amino acid-ligated cyclic metal-oxo framework. X-Ray photoelectron, UV-visible reflectance, and electron paramagnetic resonance spectroscopy, together with metal analysis, confirm the incorporation of vanadium into the polyoxometalates, while single crystal X-ray diffraction analysis supports the location of the vanadium atoms in the central core.
Publisher: Elsevier BV
Date: 09-2015
Publisher: Elsevier BV
Date: 03-2014
Publisher: American Chemical Society (ACS)
Date: 15-11-2016
DOI: 10.1021/ACS.INORGCHEM.6B02218
Abstract: Eight new members of a family of mixed-metal (Mo,W) polyoxometalates (POMs) with amino acid ligands have been synthesized and investigated in the solid state and solution using multiple physical techniques. While the peripheral POM structural framework is conserved, the different analogues vary in nuclearity of the central metal-oxo core, overall redox state, metal composition, and identity of the zwitterionic α-amino acid ligands. Structural investigations reveal site-selective substitution of Mo for W, with a strong preference for Mo to occupy the central metal-oxo core. This core structural unit is a closed tetrametallic loop in the blue reduced species and an open trimetallic loop in the colorless oxidized analogues. Density functional theory calculations suggest the core as the favored site of reduction and reveal that the corresponding molecular orbital is much lower in energy for a tetra- versus trimetallic core. The reduced species are diamagnetic, each with a pair of strongly antiferromagnetically coupled Mo
Publisher: Elsevier BV
Date: 08-2013
Publisher: Elsevier BV
Date: 09-2011
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C6RA01390B
Abstract: The reaction of sulfur ylides SMe 2 C(H)C(O)R (R = 4-nitrophenyl, phenyl, and 3-nitrophenyl) with [PdCl 2 (cod)] gives the new Pd( ii ) complexes of type cis - and trans -[PdCl 2 (SMe 2 C(H)C(O)R) 2 ] (R = phenyl ( 1 ), 3-nitrophenyl ( 2 ), and 4-nitrophenyl ( 3 )).
Publisher: Springer Science and Business Media LLC
Date: 2014
DOI: 10.2478/S11696-013-0487-5
Abstract: The reaction of dppm (1,1-bis(diphenylphosphino)methane) with 2-bromo-4-phenylacetophenone and benzyl bromoacetate in chloroform produces new phosphonium salts, [Ph2PCH2PPh2CH2C(O) C6H4Ph]Br (I) and [Ph2PCH2PPh2CH2COOCH2Ph]Br (II). By allowing the phosphonium salts to react with the appropriate base, the bidentate phosphorus ylides, Ph2PCH2PPh2=C(H)C(O)C6H4Ph (III) and Ph2PCH2PPh2=C(H)C(O)OCH2Ph (IV), were obtained. The reaction of these ligands with mercury(II) halides in dry methanol led to the formation of the mononuclear complexes {HgX2[(Ph2PCH2PPh2C(H)C(O)C6H4Ph)]} (X = Cl (V) X = Br (VI) X = I (VII)) and {HgX2[(Ph2PCH2PPh2C(H)COOCH2Ph)]} (X = Cl (VIII) X = Br (IX) X = I (X)). The FTIR and 1H, 31P and 13C NMR spectra were studied. The structure of compound III was unequivocally determined by the single-crystal X-ray diffraction technique. Single-crystal X-ray analysis of the {HgBr2[(Ph2PCH2PPh2C(H)C(O)C6H4Me)]} complex (XI) revealed the presence of a mononuclear complex containing the Hg atom in a distorted tetrahedral environment. In all complexes, the ylides referred to above were coordinated through the ylidic carbon and the phosphine atom.
Publisher: Royal Society of Chemistry (RSC)
Date: 2013
DOI: 10.1039/C2DT31902K
Abstract: Reaction of sulfonium ylides (Me)(2)SCHC(O)C(6)H(4)R (R = H m-NO(2) p-NO(2) p-OMe p-Me and p-Br) with AgNO(3) in dichloromethane leads to various compounds. Single crystal X-ray diffraction analysis reveals that the adducts take 3 forms: (i) two-dimensional polymer, [AgNO(3)(Me(2)SCHC(O)C(6)H(5))](n) (1), with nitrate bridges in which each nitrate coordinates to three silver atoms through two oxygen atoms and two Me(2)SCHC(O)C(6)H(5) ligands coordinate to silver centers through carbon atoms (ii) cationic binuclear, [Ag(Me(2)SCHC(O)C(6)H(4)-m-NO(2))(2)](2)(NO(3))(2)·2H(2)O (2), in which Me(2)SCHC(O)C(6)H(4)-m-NO(2) ligands simultaneously coordinate through both carbon and oxygen atoms with nitrate as a counter ion, and (iii) cationic mononuclear and anionic binuclear, [Ag(Me(2)SCHC(O)C(6)H(4)-p-NO(2))(2)](2)[{AgNO(3)(μ-NO(3)) (Me(2)SCHC(O)C(6)H(4)-p-NO(2))}(2)]·2CH(3)OH (3), in which nitrate groups act as bridging as well as terminal ligands, and Me(2)SCHC(O)C(6)H(4)-p-NO(2) ligands display C-coordination. Characterization of the obtained compounds was also performed by infrared, (1)H- and (13)C-NMR spectroscopy and analytical data indicated a 1 : 2 stoichiometry between the silver(I) nitrate and ylide p-OMe (4) and 1 : 1 for ylides p-Me (5) and p-Br (6). In addition, the antibacterial effects of DMSO-solutions of complexes 1-6 were evaluated by the agar disc diffusion method against three Gram positive and three Gram negative bacteria. All complexes displayed antibacterial activity against these bacteria, with high levels of inhibitory potency exhibited against the Gram negative species.
Publisher: Elsevier BV
Date: 04-2013
Publisher: Wiley
Date: 09-09-2014
Abstract: The first members of a promising new family of hybrid amino acid-polyoxometalates have emerged from a search for modular functional molecules. Incorporation of glycine (Gly) or norleucine (Nle) ligands into an yttrium-tungstoarsenate structural backbone, followed by crystallization with p-methylbenzylammonium (p-MeBzNH3(+)) cations, affords (p-MeBzNH3)6K2(GlyH)[As(III)4(Y(III)W(VI)3)W(VI)44Y(III)4O159(Gly)8(H2O)14]⋅47 H2O (1) and enantiomorphs (p-MeBzNH3)15(NleH)3[As(III)4(Mo(V)2Mo(VI)2)W(VI)44Y(III)4O160(Nle)9(H2O)11][As(III)4(Mo(VI)2W(VI)2)W(VI)44Y(III)4O160(Nle)9(H2O)11] (generically designated 2: L-Nle, 2 a D-Nle, 2 b). An intensive structural, spectroscopic, electrochemical, magnetochemical and theoretical investigation has allowed the elucidation of site-selective metal substitution and photoreduction of the tetranuclear core of the hybrid polyanions. In the solid state, markedly different crystal packing is evident for the compounds, which indicates the role of noncovalent interactions involving the amino acid ligands. In solution, mass spectrometric and small-angle X-ray scattering studies confirm maintenance of the structure of the polyanions of 2, while circular dichroism demonstrates that the chirality is also maintained. The combination of all of these features in a single modular family emphasizes the potential of such hybrid polyoxometalates to provide nanoscale molecular materials with tunable properties.
Publisher: Elsevier BV
Date: 05-2017
Publisher: Elsevier BV
Date: 02-2013
Publisher: Elsevier BV
Date: 2014
Publisher: Elsevier BV
Date: 07-2018
Publisher: Elsevier BV
Date: 10-2008
Publisher: Wiley
Date: 20-08-2019
Location: Iran (Islamic Republic of)
No related grants have been discovered for Fateme Akhlaghi Bagherjeri.