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Träfflista för sökning "WFRF:(Abu Youssef Morsy A.M.) "

Sökning: WFRF:(Abu Youssef Morsy A.M.)

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1.
  • Abu-Youssef, Morsy A.M., et al. (författare)
  • 1D, 2D and 3D cadmium(II) polymeric complexes with quinoline-4-carboxylato anion, quinazoline and 2,5-dimethylpyrazine
  • 2006
  • Ingår i: Polyhedron. - : Elsevier BV. - 0277-5387. ; 25:5, s. 1187-1194
  • Tidskriftsartikel (refereegranskat)abstract
    • Three new cadmium(II) complexes, namely [Cd(Qux)2(H2O)]n (1), [Cd(Quz)2(N3)2]n (2) and [Cd(dmpz)(N3)2]n (3) (Qux = quinoline-4-carboxylato anion, Quz = quinazoline, dmpz = 2,5-dimethylpyrazine), have been synthesized and characterized by spectroscopic and crystallographic methods. The structure of 1 contains CdO6 slightly distorted octahedral geometry around the Cd(II) atoms, axialy coordinated to two bridging water molecules forming the 1D chain and four oxygen atoms from four different μ-O,O′-bridging caboxylato groups of (Qux) in the equatorial plane. The 1D chains are further held together through hydrogen bonds between the μ-aqua molecule and the meta non-coordinated nitrogen atom of the quinoline moiety. In complex 2, two quinazoline ligands are linked to the central Cd(II) ion in a trans position through the meta hetero nitrogen atom and di(EE), (μ1,3-N3) groups and show a two dimensional (2D) topology. In complex 3 the central cadmium(II) atom is simultaneously coordinated to di(EE), (μ1,3-N3) groups (NCdN, 180.0°) forming a sheet structure in the bc plane and further bridging μ-N,N′-dimethylpyrazine ligand in the a-direction (NCdN, 180.0°) giving rise to a 3D network structure. The IR spectra of the three complexes were measured and they confirm the X-ray structural data.
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2.
  • Abu-Youssef, Morsy A.M., et al. (författare)
  • 1D and 2D FeII Azide Coordination Polymers with Ferromagnetic Canting
  • 2008
  • Ingår i: European Journal of Inorganic Chemistry. - : Wiley. - 1434-1948 .- 1099-0682. ; 2008:1, s. 112-118
  • Tidskriftsartikel (refereegranskat)abstract
    • The two compounds [FeII(pyridine)2(N3)2(H2O)] (1) and [FeII(4-acetylpyridine)2(N3)2] (2) were prepared. The X-ray crystal structures show end-to-end (EE) bridging azides in both cases with a 1D Fe-NNN-Fe chain for 1 and a 2D Fe-NNN-Fe net in 2. Both compounds show similar magnetic behaviour where the high-temperature data are consistent with antiferromagnetic couplings and the low-temperature data indicate ferrimagnetic ordering based on spin canting at 20 and 45 K. Compound 2 also shows a hysteresis loop. These findings are compared to the related 3D coordination polymer [Fe(N3)2(4,4'-bipyridine)]. According to network analyses the latter compound was shown to contain the new uninodal six-connected-network topology (510 · 64 · 7)-jsm.
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3.
  • Abu-Youssef, Morsy A.M., et al. (författare)
  • A unique example of a high symmetry three- and four-connected hydrogen bonded 3D-network
  • 2006
  • Ingår i: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1364-548X .- 1359-7345. ; 2006:10, s. 1082-1084
  • Tidskriftsartikel (refereegranskat)abstract
    • We present a three- and four-connected 3D-net based on 4-aminopyridine coordinated to Ag(I) and hydrogen bonded to nitrate with the unusual, high symmetry, topology (83)(86)2-tfa.
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4.
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5.
  • Abu-Youssef, Morsy A. M., et al. (författare)
  • Global Engagement in Science: The University’s Fourth Mission?
  • 2018
  • Ingår i: Science & Diplomacy. ; 7:2
  • Tidskriftsartikel (refereegranskat)abstract
    • In this article, the authors - three scientists and a diplomat, working across multiple continents - intend to impart some of the broad perspective and deep experience they’ve gained over the years as professionals. The diplomat among us, stationed in the Middle East, has played a role in fostering peace in a region long beset by conflict. Drawing from accumulated lessons, we intend to discuss how others can be encouraged to contribute to global science, regardless of their background or national origin. In taking on this challenge, we will share insights from our various tenures as operators of bilateral aid programs, members of international science organizations, and participants in government negotiations and other events featuring the development of global science.
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6.
  • Abu-Youssef, Morsy A. M., et al. (författare)
  • Molecular, supramolecular structures combined with hirshfeld and dft studies of centrosymmetric m(Ii)-azido {m=ni(ii), fe(ii) or zn(ii)} complexes of 4-benzoylpyridine
  • 2021
  • Ingår i: Symmetry. - : MDPI AG. - 2073-8994. ; 13:11
  • Tidskriftsartikel (refereegranskat)abstract
    • The supramolecular structures of the three metal (II) azido complexes [Fe(4bzpy)4 (N3 )2 ]; 1, [Ni(4bzpy)4 (N3 )2 ]; 2 and [Zn(4bzpy)2 (N3 )2 ]n; 3 with 4-benzoylpyridine (4bzpy) were presented. All complexes contain hexa-coordinated divalent metal ions with a slightly distorted octahedral MN6 coordination sphere. Complexes 1 and 2 are monomeric with terminal azido groups while 3 is one-dimensional coordination polymer containing azido groups with µ(1,1) and µ(1,3) bridging modes of bonding. Hirshfeld analysis was used to quantitatively determine the different contacts affecting the molecular packing in the studied complexes. The most common interactions are the polar O … H and N … H interactions and the hydrophobic C … H contacts. The charges at the M(II) sites are calculated to be 1.004, 0.847, and 1.147 e for complexes 1–3, respectively. The degree of asymmetry is the highest in the case of the terminal azide in complexes 1 and 2 while was found the lowest in the µ(1,1) and µ(1,3) azide bonding modes in the Zn(II) complex 3. These facts were further explained in terms of atoms in molecules (AIM) topological parameters.
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7.
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8.
  • Abu-Youssef, Morsy A. M., et al. (författare)
  • New homogeneous and alternating Mn(II)-azido 1D systems
  • 2005
  • Ingår i: Polyhedron. - : Elsevier BV. - 0277-5387. ; 24:4, s. 557-562
  • Tidskriftsartikel (refereegranskat)abstract
    • Reaction of sodium azide with manganese(II) and 4-amino-1,2,4-triazol or 3-chloropyridine leads to the 1D systems [Mn(N-3)(2) (4-amtr)(2)](,) (1) or {[Mn(N-3)(2)(3-Clpy)(2)]center dot 1/2(3-Clpy)}(n) (2), respectively. Compound 1 crystallises in the C2/m (monoclinic) group and consists of chains of Mn(II) cations bridged by double mu(1,3)-azido bridges in trans arrangement. Compound 2 crystallises in the I2/a (monoclinic) group and in this case the 1D system shows alternating double mu(1,1) and mu(1,3) bridges. Magnetic properties follow the expected antiferromagnetic (compound 1) and alternating ferro-antiferromagnetic (compound 2) behaviour. (c) 2005 Published by Elsevier Ltd.
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9.
  • Abu-Youssef, Morsy A. M., et al. (författare)
  • New Polymeric Manganese Azide Derivatives with Quinazoline
  • 2005
  • Ingår i: European Journal of Inorganic Chemistry. - 1434-1948 .- 1099-0682. ; 2005:22, s. 4659 - 4664
  • Tidskriftsartikel (refereegranskat)abstract
    • Two new polymeric derivatives of the (azido)MnII system with formula [Mn(H2O)(μ-N3)(N3)(quinaz)2]n (1) and [Mn(μ-N3)2(quinaz)2]n (2) (quinaz = quinazoline) have been structurally and magnetically characterised. Compound 1 crystallises in the triclinic system, space group P-1, and consists of 1D chains with single end-to-end azido bridges. These chains give a two-dimensional supramolecular arrangement by means of H-bond interactions. Compound 2 crystallises in the monoclinic system, space group C2/c, and contains a square alternating 2D network bridged by azido ligands in the end-to-end coordination mode. Compound 2 exhibits some unusual features, such as the unprecedented linear coordination of the azido bridge. Magnetic analysis reveals moderate antiferromagnetic coupling, with J values in good agreement with the expected range, as a function of the Mn-N-N bond angles.
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10.
  • Abu-Youssef, Morsy A.M., et al. (författare)
  • Synthesis, a case of isostructural packing, and antimicrobial activity of silver(I)quinoxaline nitrate, silver(I)(2,5-dimethylpyrazine) nitrate and two related silver aminopyridine compounds
  • 2006
  • Ingår i: Dalton Transactions. - : Royal Society of Chemistry (RSC). - 1477-9226 .- 1477-9234. ; 2006:21, s. 2542-2550
  • Tidskriftsartikel (refereegranskat)abstract
    • The synthesis and low temperature crystal structures of [Ag(quinoxaline)]n(NO3)n, 1, [Ag(2,5-dimethylpyrazine)(NO3)]n, 2 and [Ag4(3-aminopyridine)4(NO3)4]n 3 are presented. The quinoxaline compound forms a 1D coordination polymer with the characteristic linear 2-coordination figure of silver(I), the NAgN angle being 164.2(1)°, and only weak silvernitrate interactions. In addition there is an interaction giving pairs of parallel chains as the main structural theme. The 2,5-dimethylpyrazine compound has approximately trigonal-planar coordination, also binding one nitrate at the relatively short AgO distances 2.444(3)Å and 2.484(3)Å, respectively, for the two crystallographically different silver atoms. This also results in a 1D coordination polymer that, despite the large differences in the Ag(I) coordination environment, is isostructural with 1. [Ag4(3-aminopyridine)4(NO3)4]n 3 forms a 2D coordination polymer by bridging nitrate ions. The antimicrobial activity of 13, and also of [Ag3(2-aminopyridine)4](NO3)3, 4 was screened for 13 different pathogens and substantial activity was shown for 1 against Escherichia coli and Pseudomonas aeruginosa (MIC 4 µg cm3) and somewhat lower activity was registered against Sarcina lutea and Salmonella typhi for 1, Bordetella bronchiseptica for 2, Salmonella typhi and Pseudomonas aeruginosa for 3, and Escherichia coli and Shigella sonnie for 3 (MIC 8 µg cm3). Only low activity was shown against the yeast Candida albicans for 1, 2 and 4 whereas no activity against this pathogen was registered for 3.
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11.
  • Abu-Youssef, Morsy A.M., et al. (författare)
  • Synthesis and Structure of Silver Complexes with Nicotinate-Type Ligands Having Antibacterial Activities against Clinically Isolated Antibiotic Resistant Pathogens
  • 2007
  • Ingår i: Inorganic Chemistry. - : American Chemical Society (ACS). - 0020-1669 .- 1520-510X. ; 46:15, s. 5893-5903
  • Tidskriftsartikel (refereegranskat)abstract
    • The synthesis and low-temperature X-ray crystal structures of five new silver complexes, [Ag2-μ-O,O'(2-aminonicotinium)2(NO3)2]n (7), [Ag(isonicotinamide)2-μ-O,O'(NO3)]2 (8), [Ag(ethyl nicotinate)2](NO3) (9), [Ag(ethyl isonicotinate)2(NO3)] (10), and [Ag(methyl isonicotinate)2(H2O)](NO3) (11), are presented and fully characterized by spectral and elemental analysis. The antimicrobial activities of these complexes were screened using 12 different clinical isolates belonging to four pathogenic bacteria, S. aureus, S. pyogenes, P. mirabilis, and Ps. Aeruginosa, all obtained from diabetic foot ulcers. These tested bacteria were resistant for at least 10 antibiotics commonly used for treatment of diabetic foot ulcers. Compounds 7 and 8 had considerable activity against Ps. Aeruginosa (MIC values 2-8 µg/mL), compound 9 against S. aureus (MIC 4-16 µg/mL) and S. pyogenes (MIC 2-4 µg/mL), and also 9 and 11 against P. mirabilis (MIC 1-16 µg/mL). All complexes were non-toxic for daphnia at concentrations above 512 µg/mL overnight.
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12.
  • Abu-Youssef, Morsy A. M., et al. (författare)
  • Synthesis, Crystal Structure, Quantum Chemical Calculations, DNA Interactions, and Antimicrobial Activity of [Ag(2-amino-3-methylpyridine)2]NO3 and [Ag(pyridine-2-carboxaldoxime)NO3]
  • 2010
  • Ingår i: Inorganic Chemistry. - : American Chemical Society (ACS). - 0020-1669 .- 1520-510X. ; 49:21, s. 9788-9797
  • Tidskriftsartikel (refereegranskat)abstract
    • [Ag(2-amino-3-methylpyridine)2]NO3 (1) and [Ag(pyridine-2-carboxaldoxime)NO3] (2) were prepared from corresponding ligands and AgNO3 in water/ethanol solutions, and the products were characterized by IR, elemental analysis, NMR, and TGA. The X-ray crystal structures of the two compounds show that the geometry around the silver(I) ion is bent for complex 1 with nitrate as an anion and trigonal planar for complex 2 with nitrate coordinated. ESI-MS results of solutions of 2 indicate the independent existence in solution of the [Ag(pyridine-2-carboxaldoxime)]+ ion. The geometries of the complexes are well described by DFT calculations using the ZORA relativistic approach. The compounds were tested against 14 different clinically isolated and four ATCC standard bacteria and yeasts and also compared with 17 commonly used antibiotics. Both 1 and 2 exhibited considerable activity against S. lutea, M. lutea, and S. aureus and against the yeast Candida albicans, while 2-amino-3-methylpyridine is slightly active and pyridine-2-carboxaldoxime shows no antimicrobial activity. In addition, the interaction of these metal complexes with DNA was investigated. Both 1 and 2 bind to DNA and reduce its electrophoretic mobility with different patterns of migration, while the ligands themselves induce no change.
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13.
  • Abu-Youssef, Morsy A.M., et al. (författare)
  • Synthesis, Structure, and Magnetic Behavior of Two New 1D Polymeric Manganese Azido Complexes
  • 2006
  • Ingår i: European Journal of Inorganic Chemistry. ; 2006:16, s. 3177-3184
  • Tidskriftsartikel (refereegranskat)abstract
    • Two new MnII one-dimensional compounds with formulae [Mn(μ-N3)2(pyzamid)2]n (1) and [Mn2(3-ampy)4(μ-N3)2(N3)2(H2O)2]n, (2) (pyzamid = pyrazineamide and 3-ampy = 3-aminopyridine) were structurally and magnetically characterized. Compound 1 crystallizes in the monoclinic system, P2/c space group, and polymerizes through double end-on azido bridges giving 1D chains with the MnII atoms in a MnN6 environment. Compound 2 crystallizes in the triclinic system, P-1 space group, and consists of alternate [Mn(3-ampy)2(μ-N3)2(N3)2] and [Mn(3-ampy)2(μ-N3)2(H2O)2] octahedrons (MnN6 - MnN4O2 environments), linked by single end-to-end azido bridges. Both chains show very uncommon topologies. Attemps to obtain manganese/azido derivatives with the qux = quinoline-4-carboxylato anion gave the recently reported compound [Mn(μ-qux)2(μ-H2O)]n (3), which consists of a chain with only carboxylato and aqua bridges with the MnII atoms in a MnO6 slightly distorted octahedron. In good agreement with the expected behavior, magnetic susceptibility measurements show weak ferromagnetic interactions for 1, whereas compound 2 exhibits moderate antiferromagnetic coupling.
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14.
  • Abu-Youssef, Morsy A. M., et al. (författare)
  • Synthesis, structure, network and thermal analysis of four 5-(pyrazinyl)tetrazolato copper(II) and cobalt(II) complexes
  • 2007
  • Ingår i: Polyhedron. - : Elsevier BV. - 0277-5387. ; 26:7, s. 1531-1540
  • Tidskriftsartikel (refereegranskat)abstract
    • Three new copper complexes and one cobalt complex with 5-(pyrazinyl)tetrazolate anion, (pyztz)(-), as chelating bidentate ligand, were obtained by the reaction of pyrazinecarbonitrile with sodium azide in the presence of copper(II) nitrate or cobalt(II)chloride. Complexes of composition [Cu(pyztz)(2)(H2O)] (1) deep blue crystals, [Cu(pyztz)(2)(H2O)(2)] (2a) green crystals, [Co(pyztz)(2)(H2O)(2)] (2b) orange crystals, [Cu(pyztz)2(H2O)(2)] center dot (H2O) (3) blue crystals were obtained. The single crystal X-ray diffraction revealed that complex I has square pyramidal structure with one water molecule at apical and two pyrazine-tetrazolato ligands at basal sites, while structures of 2a, 2b and 3 consist of octahedrally coordinated metal ions, where two pyztz anions act as bidentate ligands via one of the pyrazine-N atoms and one of the tetrazole-N atoms in trans-positions and two trans water molecules. Complex 3 contains one extra lattice water molecule. Hydrogen bonds of the types O-H center dot center dot center dot O and O-H center dot center dot center dot N connect the mononuclear units to a three-dimensional network structure in 2 (a and b are isostructural) and 3. Although the H-bond patterns look complex it is shown that they can be related to the well-known three- and six-connected rutile net (rtl) in 2 and the four- and six-connected fsh-net in 3. (C) 2006 Elsevier Ltd. All rights reserved.
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15.
  • Abu-Youssef, Morsy A. M., et al. (författare)
  • Topology Analysis Reveals Supramolecular Organisation of 96 Large Complex Ions into one Geometrical Object
  • 2016
  • Ingår i: CrystEngComm. - : Royal Society of Chemistry (RSC). - 1466-8033. ; 18:11, s. 1883-1886
  • Tidskriftsartikel (refereegranskat)abstract
    • It is shown that the highly complex crystal structure of [Ag(4-(pyrrolidin-1-yl)pyridine)2]NO3·1/2H2O, 1, with 12 symmetry-independent Ag+ ions and 96 units of complex ions in a unit cell can be understood by the ubiquitous srs topology, reducing thousands of atom positions into a single geometrical object in one go.
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16.
  • Ghazzali, Mohamed I D M, 1974, et al. (författare)
  • 4,4'-(Azinodimethylene)dipyridinium bis(tetrafluoroborate) and 4-[(4-pyridylmethylene)hydrazonomethyl]pyridinium perchlorate: two different hydrogen-bonding motifs
  • 2007
  • Ingår i: Acta Crystallographica Section C: Crystal Structure Communications. - 0108-2701 .- 1600-5759. ; C63:5, s. o312-o314
  • Tidskriftsartikel (refereegranskat)abstract
    • In the crystal structures of the title compounds, C12H12N42+·2BF4-, (I), and C12H11N4+·ClO4-, (II), respectively, infinite two- and one-dimensional architectures are built up via N-H...F [in (I)] and conventional N-H...N [in (II)] hydrogen bonding. The N-N single bond in (I) lies on a crystallographic centre of symmetry; as a result, the two pyridinium rings are parallel. In (II), the pyridinium and pyridyl ring planes are inclined with a dihedral angle of 14.45(3)°.
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17.
  • Ghazzali, Mohamed I D M, 1974, et al. (författare)
  • catena-Poly[[chloro(pyridinium-3-carboxylato-κO)zinc(II)]-μ-nicotinato-κ2O:N]
  • 2007
  • Ingår i: Acta Crystallographica Section E: Structure Reports Online. - 1600-5368. ; E63:1, s. m114-m116
  • Tidskriftsartikel (refereegranskat)abstract
    • The title bis-nicotinate zinc chloride, [Zn(C6H4NO2)Cl(C6H5NO2)]n, has an infinite head-to-tail one-dimensional chain structure. The compound was synthesized under mild hydrothermal conditions. The ZnII atom exhibits a distorted tetrahedral coordination geometry. The structure is statistically disordered, with 0.5 site occupancy for the Zn atom and the H atom located on the pyridine N atom. As a result, Zn positions in the crystal structure alternate between two sites related by a crystallographic twofold axis and rows of molecules are formed, supported by strong N-H...O hydrogen bonds.
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18.
  • Ghazzali, Mohamed I D M, 1974, et al. (författare)
  • Synthesis, EPR and DFT calculations of rare Ag(II)porphyrins and the crystal structure of [Zn(II)tetrakis(4-bromo-2-thiophene)porphyrin]
  • 2008
  • Ingår i: Inorganic Chemistry Communication. - : Elsevier BV. - 1387-7003 .- 1879-0259. ; 11:9, s. 1019-1022
  • Tidskriftsartikel (refereegranskat)abstract
    • Meso-tetrakis (4-bromo-2-thiophene) and (5-bromo-2-thiophene) porphyrins were synthesized in 18% yield from freshly distilled pyrrole and the corresponding aldehydes in refluxing propionic acid. Reaction of both porphyrins with either Zn(OAc) 2 · 2H 2 O or Ag(OAc) afforded the corresponding metal complexes in 20% yield. The free bases and metal complexes were characterized by IR, NMR, EPR, MS and XPS. The crystal structure of 5,10,15,20(4-bromo-2-thiophene)porphyrinato Zn(II) was determined by X-ray diffraction and shows a 'zigzag-like' packing pattern due to S···S intermolecular interaction. Structural features of these molecules are discussed by DFT quantum chemical calculations. © 2008 Elsevier B.V. All rights reserved.
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19.
  • Massoud, Al-Shimaà A A, 1980, et al. (författare)
  • 2D Bipyrimidine silver(I) nitrate: Synthesis, X-ray structure, solution chemistry and anti-microbial activit
  • 2011
  • Ingår i: Inorganic Chemistry Communication. - : Elsevier BV. - 1387-7003. ; 14:4, s. 550-553
  • Tidskriftsartikel (refereegranskat)abstract
    • Synthesis and X-ray single crystal structure analysis of the compound {[Ag2(μ2-bpym)(μ-O-NO3)2]}n, (1), (where bpym = 2,2′-bipyrimidine) are presented. Compound (1) has a (6,3)-2D honeycomb structure with a tetrahedral coordination geometry around the Ag(I) ion. In contrary to the solid state structural investigation, ESI-MS for (1) in solution shows a strong peak at m/z 423.0269 which indicates that the [Ag(bpym)2]+ cation is dominating instead of [Ag2(bpym)]2+. The anti-microbial activity of (1) was screened against 15 multi-drug resistant bacteria in comparison to silver(I) sulphadiazine and it showed a high activity against Burkholderia mallei which causes glanders; with a MIC value of 4 μg/ml.
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20.
  • Massoud, Al-Shimaà A A, 1980, et al. (författare)
  • Bis 4,5-diazafluoren-9-one silver(I) nitrate: synthesis, X-ray structures, solution chemistry, hydrogel loading, DNA coupling and anti-bacterial screening
  • 2011
  • Ingår i: New Journal of Chemistry. - : Royal Society of Chemistry (RSC). - 1369-9261 .- 1144-0546. ; 35:3, s. 640-648
  • Tidskriftsartikel (refereegranskat)abstract
    • Synthesis of bis-4,5-diazafluoren-9-one silver(I) nitrate I (dafone = 4,5-diazafluoren-9-one) and the low temperature X-ray single crystal structure of [Ag(4,5-diazafluoren-9-one)2NO3], crystal form 1, and a re-determination of [Ag(4,5-diazafluoren-9-one)2]NO3 . H2O, crystal form 2 are presented. Crystal form 1 has a distorted trigonal planar coordination geometry around Ag(I) with an N-Ag-N bond angle of 123.45(7)o. Crystal form 2 has a perfect linear coordination around Ag, with N-Ag-N 180.0o. Compound I was characterized by 1H-NMR, biological activity and ESI-MS in DMSO at room temperature. The biological activity was determined against 6 different resistant clinical isolates; two Gram-positive (Staphylococcus aureus and Streptococcus pyogenes) and four Gram-negative (Pseudomonas aeruginosa, Klebsiella pneumoniae, Proteus mirabilis, and Salmonella sp.) in comparison with 15 known antibiotics used in the treatment of diabetic foot infections. Compound I showed broad spectrum activity against all the test organisms. P. mirabilis and S. aureus and K. pneumoniae were the most sensitive clinical isolates (MIC = 4, 6 and 4 μg ml-1, respectively). Three different hydrogels containing I or Ag2SO4 were prepared and the antimicrobial activity against Ps. aeruginosa (ATCC 15442) compared, showing more or less equal activity on a weight basis, but I seems to have a significant better performance per silver ion. The Ag(I) complex also binds more effectively to calf thymus DNA than the dafone ligand itself.
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21.
  • Massoud, Al-Shimaà A A, 1980, et al. (författare)
  • Bis[4-(dimethylamino)pyridine-κN1]silver(I) nitrate dihydrate
  • 2009
  • Ingår i: Acta Crystallographica Section C: Crystal Structure Communications. - 0108-2701 .- 1600-5759. ; C65:9, s. m352-m354
  • Tidskriftsartikel (refereegranskat)abstract
    • The title compound, [Ag(C7H10N2)2]NO3·2H2O or [Ag(dmap)2]NO3·2H2O, where dmap is 4-(dimethylamino)pyridine, has a distorted linear coordination geometry around the AgI ion. A novel pattern of water-nitrate hydrogen-bonded anionic strands is formed in the c direction, with the cationic [Ag(dmap)2]+ monomers trapped between them. The AgI ion and the nitrate group atoms, as well as the water molecules (including the H atoms), are on a crystallographic mirror plane (Wyckoff position 4a). The influence of bulky methyl substituents in position 4 of the 4-(dimethylamino)pyridine ligand on packing is discussed. The absolute structure was determined unequivocally.
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22.
  • Massoud, Al-Shimaà A A, 1980, et al. (författare)
  • Effects of Different Substituents on the Crystal Structures and Antimicrobial Activities of Six Ag(I) Quinoline Compounds
  • 2013
  • Ingår i: Inorganic Chemistry. - : American Chemical Society (ACS). - 0020-1669 .- 1520-510X. ; 52:7, s. 4046-4060
  • Tidskriftsartikel (refereegranskat)abstract
    • The syntheses and single crystal X-ray structures of [Ag(5-nitroquinoline)(2)]NO3 (1), [Ag(8-nitroquinoline)(2)]NO3 center dot H2O (2), [Ag(6-methoxy-8-nitroquinoline)(NO3)](n) (3), [Ag(3-quinolinecarbonitrile)(NO3)](n) (4), [Ag(3-quinolinecarbonitrile)(2)]NO3 (5), and [Ag(6-quinolinecarboxylic acid)(2)]NO3 (6) are described. As an alternative to solution chemistry, solid-state grinding could be used to prepare compounds 1 and 3, but the preparation of 4 and 5 in this way failed. The Ag(I) ions in the monomeric compounds 1, 2, 5, and 6 are coordinated to two ligands via the nitrogen atoms of the quinoline rings, thereby forming a distorted linear coordination geometry with Ag-N bond distances of 2.142(2)-2.336(2) angstrom and N-Ag-N bond angles of 163.62(13)degrees-172.25(13)degrees. The 1D coordination polymers 3 and 4 contain Ag(I) centers coordinating one ligand and two bridging nitrate groups, thereby forming a distorted trigonal planar coordination geometry with Ag-N bond distances of 2.2700(14) and 2.224(5) angstrom, Ag-O bond distances of 2.261(4)-2.536(5) angstrom, and N-Ag-O bond angles of 115.23(5)degrees-155.56(5)degrees. Hirshfeld surface analyses of compounds 1-6 are presented as d(norm) and curvedness maps. The d(norm) maps show different interaction sites around the Ag(I) ions, i.e., Ag center dot center dot center dot Ag interactions and possible O-H center dot center dot center dot O, C-H center dot center dot center dot O, C-H center dot center dot center dot N, and C-H center dot center dot center dot C hydrogen bonds. Curvedness maps are a good way of visualizing pi-pi tacking interactions between molecules. The antimicrobial activities of compounds 1, 2, and 6 were screened against 15 different multidrug-resistant strains of bacteria isolated from diabetic foot ulcers and compared to the antimicrobial activities of the clinically used silver sulfadiazine (SS). Compound 2 showed activity similar to SS against this set of test organisms, being active against all strains and having slightly better average silver efficiency than SS (5 vs 6 mu g Ag/mL). Against the standard nonresistant bacterial strains of Staphylococcus aureus, Pseudomonas aeruginosa, Proteus mirabilis, and Streptococcus pyogenes, compound 1 performed better than silver nitrate, with an average MIC of 6 mu g Ag/mL versus 18 mu g Ag/mL for the reference AgNO3. Electrospray ionization mass spectrometry (ESI-MS) analyses of compounds 3 and 6 in DMSO/MeOH confirm the two-coordinated Ag+ complexes in solution, and the results of the H-1 NMR titrations of DMSO solutions of 5-nitroquinoline and 8-nitroquinoline with AgNO3 in DMSO suggest that 5-nitroquinoline is more strongly coordinated to the silver ion.
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23.
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24.
  • Massoud, Al-Shimaà A A, 1980, et al. (författare)
  • Synthesis, X-ray structure and anti-corrosion activity of two silver(I) pyrazino complexes
  • 2009
  • Ingår i: Polyhedron. - : Elsevier BV. - 0277-5387. ; 28:13, s. 2794-2802
  • Tidskriftsartikel (refereegranskat)abstract
    • Two new silver(I) pyrazine complexes [Ag2(ampyz)(NO3)2]n, 1 and {[Ag(2,3-pyzdic)](NO3)}n, 2 (where ampyz = aminopyrazine, and 2,3-pyzdic = 2,3-pyrazinedicarboxamide) were synthesized and structurally characterized by X-ray single crystal structure analysis. Complex 1 has a 2D sheet structure through both bridging μO,O′-(NO3) groups and μN,N′-pyrazine moieties. A 3D structure with a characteristic (10,3)-d or 103-utp net is formed through extensive hydrogen bonding. Complex 2 has a 1D chain structure through bridging μN,N′-pyrazine moieties. Strong hydrogen bonds further connect these chains to extend the dimensionality to a 3D network structure. The complexes were tested as corrosion inhibitors for mild steel in 0.1 M nitric acid medium using potentiodynamic polarization technique. Both complexes are of mixed type corrosion inhibitors with dominant anodic effect. The inhibition efficiencies are 68% and 50% for complexes 1 and 2, respectively. The inhibition mechanisms of both inhibitors are mainly due to adsorption of the inhibitor molecules on the surface of mild steel. All data were compared and fitted to the kinetic-thermodynamic model. The binding constants K are 3263 and 1147 for complexes 1 and 2, respectively.
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25.
  • Massoud, Al-Shimaà A A, 1980, et al. (författare)
  • The coordination polymer poly[(μ3-3-aminocarbonylpyrazine-2-carboxylato-κ3N1:O2:O2')silver(I)]
  • 2011
  • Ingår i: Acta Crystallographica Section C: Crystal Structure Communications. - 0108-2701 .- 1600-5759. ; C67:1, s. m1-m4
  • Tidskriftsartikel (refereegranskat)abstract
    • The title compound, [Ag(C6H4N3O3)]n or [Ag(pyzca)]n (where pyzca is 3-aminocarbonylpyrazine-2-carboxylate), (I), was obtained by silver-catalysed partial hydrolysis of pyrazine-2,3-dicarbonitrile in aqueous solution. The compound has a distorted trigonal-planar coordination geometry around the AgI ion, with each ligand bridging three AgI ions to form a one-dimensional strand of molecules parallel to the b axis. An extensive hydrogen-bond pattern connects these strands to form a three-dimensional network of mog topology.
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26.
  • Massoud, Al-Shimaà A A, 1980, et al. (författare)
  • Two 2-D copper(II) azido compounds: catena-poly[di-μ1,1- azido,di-μN,O-(quinolinecarboxylato)(aqua)copper(II)] and 1-D catena-poly[di-μN,N'-(quinoxaline)copper(II)nitrate]
  • 2009
  • Ingår i: Journal of Coordination Chemistry. - : Informa UK Limited. - 0095-8972 .- 1029-0389. ; 62:4, s. 519-530
  • Tidskriftsartikel (refereegranskat)abstract
    • We synthesized three copper(II) complexes with two structurally related polydentate ligands,quinoline-4-carboxylic acid (quCOOH) and quinoxaline (qux). The structures of these complexes were determined using X-ray single crystal crystallography. Complex 1,[Cu(quCOO)(N3)(H2O)]n, has a 2-D polymeric structure through di-μ1,1 azido groups forming (Cu2N2) dimeric units and di-μN,O quinoline carboxylate bridging the binuclear copper units.[Cu(quCOO)(N3)(H2O)]n . 0.87MeOH, (2), has the same structure as 1 in addition to MeOH molecules separating the 2-D sheets of [Cu(quCOO)(N3)(H2O)]n. [Cu(qux)(NO3)2]n, (3), has nocoordinated azido groups, but the quinoxaline is a bidentate bridging ligand giving a 1-D chain,while the μO,O' chelating nitrato groups stabilize the chain structure by forming a square planarcoordination sphere around copper. IR and UV–Vis spectra of the complexes are in agreementwith the crystal structures.
  •  
27.
  • Mautner, F. A., et al. (författare)
  • 1D and 3D coordination polymers with the M(mu(1),mu(1)-X)(2)M motif (M = Na, Zn, Cd): Observation of a linear [Na(H2O)(4)](n)(n+) cation and a five-connected sqp-net
  • 2007
  • Ingår i: Polyhedron. - : Elsevier BV. - 0277-5387. ; 26:12, s. 2703-2712
  • Tidskriftsartikel (refereegranskat)abstract
    • Three polymeric complexes [Zn(pydz)(N-3)(SO4)](n)[Na(H2O)(4)](n)(H2O)(4n) (1), [Cd(3-ampy)(N-3)Cl](n) (2), and [Cd(DENA)Cl-2(H2O)](n)(3), (pydz = pyridazine or 1,2-diazine, 3-ampy = 3-aminopyridine, DENA = NN-diethylnicotineamide) have been synthesized and characterized by spectral and structural methods and their network topologies analysed. Complex 1 crystallizes in monoclinic C-centred space group C2/m, the Zn(1) center is octahedrally coordinated; and simultaneously bridged by EO-azido, NN'-pydz, and O,O'-sulphato ligands. The ZnN4O2-octahedra form a ID anionic chain along b-axis. The Na(OH2)(6)-octahedra have also common water molecules, thus also forming a 1D chain along b-axis. The cationic and anionic chains are connected via hydrogen bonds of type O-H...O including lattice water molecules to form a supramolecular 3D network structure. In complex 2, the Cd(1) is six-coordinated by two EE-bridging azide groups, and two nitrogen atoms of bridging NN', 3-ampy ligand, and two bridging chloro ligands. The three different bridging ligands connect the distorted octahedra of the Cd(II) centres to form a 3D network structure with the topology of a square pyramidal net (4(3) (.) 6(6)-sqp). The centrosymmetric Cd2Cl2-rings are planar and the NH2- of the 3-ampy groups forms additional hydrogen bonds of type N-H...N to the adjacent azido groups. In complex 3, the octahedrally coordinated Cd(1) centres are occupied by alternating monodentate DENA ligand and a water molecule and the other four sites are occupied by four bridging chloro ligands. Thus the Cd2Cl2-rings form common edges to form 1D chains of Cd(II) octahedra along the b-axis of the monoclinic unit cell. 2D supramolecular sheets extended along the bc-planes of the unit cell are formed by the 0-H...O hydrogen bond. The IR spectra of the three complexes were measured and they confirm the X-ray structural data. (C) 2007 Elsevier Ltd. All rights reserved.
  •  
28.
  • Soliman, S.M., et al. (författare)
  • Towards the chemical control of molecular packing: syntheses and crystal structures of three trans-[NiL4(NCS)2] complexes
  • 2014
  • Ingår i: Acta Crystallographica Section B: Structural Science, Crystal Engineering and Materials. - 2052-5206 .- 2052-5192. ; 70:1, s. 115-125
  • Tidskriftsartikel (refereegranskat)abstract
    • Three nickel(II) isothiocyanato complexes of the formulatrans-[NiL4(NCS)2] (L = ethylisonicotinate, methylisonicotinateand 4-benzoylpyridine) have been prepared: [Ni(ethylisonicotinate)4(NCS)2] (I), [Ni(methylisonicotinate)4(NCS)2](II) and [Ni(4-benzoylpyridine)4(NCS)2] (III). All threecomplexes are monomeric and have a distorted octahedralgeometry around NiII. Despite their apparent molecularsimilarity, the crystal density of (III) (1.454 g cm 3) issignificantly higher than that of (I) and (II) (both1.408 g cm 3), suggesting that the molecular packing is mostefficient in (III). A study of the molecular Hirshfeld surfaces,together with density functional theory (DFT) calculations,provide insights into the origin of the molecular packingfeatures, and it is suggested that the greater crystal density of(III) results from smaller intermolecular electrostatic repulsions.
  •  
29.
  • Yousri, Amal, et al. (författare)
  • A Novel Na(I) Coordination Complex with s-Triazine Pincer Ligand: Synthesis, X-ray Structure, Hirshfeld Analysis, and Antimicrobial Activity
  • 2023
  • Ingår i: Crystals. - 2073-4352. ; 13:6
  • Tidskriftsartikel (refereegranskat)abstract
    • The pincer ligand 2,4-bis(3,5-dimethyl-1H-pyrazol-1-yl)-6-methoxy-1,3,5-triazine (bpmt) was used to synthesize the novel [Na(bpmt)(2)][AuCl4] complex through the self-assembly method. In this complex, the Na(I) ion is hexa-coordinated with two tridentate N-pincer ligands (bpmt). The two bpmt ligand units are meridionally coordinated to Na(I) via one short Na-N(s-triazine) and two slightly longer Na-N-(pyrazole) bonds, resulting in a distorted octahedral geometry around the Na(I) ion. In the coordinated bpmt ligand, the s-triazine core is not found to be coplanar with the two pyrazole moieties. Additionally, the two bpmt units are strongly twisted from one another by 64.94 & DEG;. Based on Hirshfeld investigations, the H & BULL;& BULL;& BULL;H (53.4%) interactions have a significant role in controlling the supramolecular arrangement of the [Na(bpmt)(2)][AuCl4] complex. In addition, the Cl & BULL;& BULL;& BULL;H (12.2%), C & BULL;& BULL;& BULL;H (11.5%), N & BULL;& BULL;& BULL;H (9.3%), and O & BULL;& BULL;& BULL;H (4.9%) interactions are significant. Antimicrobial investigations revealed that the [Na(bpmt)(2)][AuCl4] complex has promising antibacterial and antifungal activities. The [Na(bpmt)(2)][AuCl4] complex showed enhanced antibacterial activity for the majority of the studied gram-positive and gram-negative bacteria compared to the free bpmt (MIC = 62.5-125 & mu;g/mL vs. MIC = 62.5-500 & mu;g/mL, respectively) and Amoxicillin (MIC > 500 & mu;g/mL) as a positive control. Additionally, the [Na(bpmt)(2)][AuCl4] complex had better antifungal efficacy (MIC = 125 & mu;g/mL) against C. albicans compared to bpmt (MIC = 500 & mu;g/mL).
  •  
30.
  • Yousri, Amal, et al. (författare)
  • Synthesis, structure diversity, and antimicrobial studies of Ag(i) complexes with quinoline-type ligands
  • 2023
  • Ingår i: CrystEngComm. - 1466-8033. ; 25:27, s. 3922-3930
  • Tidskriftsartikel (refereegranskat)abstract
    • Compounds [Ag(5NO2Qu)2]BF4 (1) and [Ag(Qu3CN)(H2O)]BF4 (2) were prepared and studied from a structural perspective and screened for antimicrobial activity. The Ag(i) in the monomeric complex 1 is coordinated to two 5-nitroquinoline (5NO2Qu) ligands via the N-atoms of the quinoline rings with equidistant Ag-N bonds (2.146(2) Å) and a N-Ag-N# bond angle of 171.42(8)°. The 2D coordination polymer 2 contains tetracoordinated Ag(i) with two N-atoms (N1 and N2#1) from two quinoline-3-carbonitrile (Qu3CN) ligands and two O-atoms (O1 and O1#1) from two water molecules. The Qu3CN ligand acts as a connector between the Ag(i) sites along the b-direction via two short Ag1-N1 (2.185(4) Å) and Ag1-N2#1 (2.204(4) Å) bonds. In addition, the Ag(i) is coordinated with two symmetry related water molecules which are also acting as connectors between the Ag(i) sites along the a-direction via two longer Ag1-O1 (2.470(4) Å) and Ag1-O1#2 (2.546(4) Å) bonds. Hirshfeld surface analysis confirmed the significance of the polar F⋯H contacts in the molecular packing of 1 (25.9%) and 2 (39.9%). In addition, the crystal packing of 1 showed a significant amount of polar O⋯H (23.5%) contacts. Also, both complexes displayed π-π stacking interactions. The Ag(i) complexes and the free ligand were assessed for their antimicrobial activities. It was found that 1 (MIC = 7.8 μg mL−1) and 2 (MIC = 31.25 μg mL−1) have higher antifungal potency against C. albicans than their free ligands (MIC = 125 μg mL−1). Interestingly, 1 has better antifungal activity than the standard nystatin (15.6 μg mL−1). Also, both Ag(i) complexes and the free ligands as well have better activity against P. mirabilis than the common antibiotic amoxicillin.
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31.
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