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276 citations found for EL AMMARI, L.

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In the title compound, C19H21N3O5S·H2O, the central indazole system is essentially planar (r.m.s. deviation = 0.012 Å), while both the benzene ring and the mean plane defined by the non-H atoms of the ethyl propionic ester unit (r.m.s. deviation = 0.087 Å) are nearly perpendicular to the indazole plane, as indicated by the dihedral angles of 82.45 (8) and 75.62 (8)°, respectively. Consequently, the mol­ecule adopts a U-shaped geometry. In the crystal, the water mol­ecule, which is linked to the indazole system by a strong O-H...N hydrogen bond, is also involved in two additional N-H...O and O-H...O inter­actions, which link the organic mol­ecules into chains along the b-axis direction.

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The mol­ecular structure of the title compound, C28H22N2O6S2·0.5CH3COOH, is built up from three fused rings, two six and one eight membered. The eight-membered ring shows a boat conformation and the dihedral angle between the two benzene groups attached thereto is 66.43 (11)°, resulting in a V-shaped geometry. Two tosyl substituents are bound to the N atoms. The planes through the tolyl rings are roughly perpendicular, as indicated by the dihedral angle of 82.44 (12)°. In the crystal, the mol­ecule and its inversion-related symmetry-equivalent are linked to the acetic acid solvent mol­ecule by non-classical O-H...O and C-H...O hydrogen bonds. Two half-occupied acetic acid solvent mol­ecules are disordered at the same site and linked by a center of symmetry.

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The fused five- and three six-membered rings of the anthra[1,2-d]imidazole­trione part of the title compound, C27H20N4O4, show two different substituents at the imidazole N atoms, viz. an allyl group and a [3-(pyridin-4-yl)-4,5-di­hydro­isoxazol-5-yl]methyl group. The fused-ring system is approximately planar [r.m.s. deviation = 0.232 (2) Å], but is slightly buckled along the common edge of the two pairs of adjacent rings, with a dihedral angle between them of 11.17 (6)°. The isoxazole ring makes dihedral angles of 27.2 (2) and 12.7 (2)° with the imidazole and pyridine rings, respectively. Weak C-H...O and C-H...N hydrogen bonds ensure the cohesion of the crystal structure, forming a three-dimensional network.

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The title compound, C23H20N2O7, consists of three fused six-membered rings (A, B and C) and one five-membered ring (D), linked to two ethyl acetate groups. The four fused rings are slightly folded around the O=C...C=O direction of the anthraquinone system, with a dihedral angle of 3.07 (8)° between the fused five- and six-membered rings (C and D) and the terminal ring (A). The planes through the atoms forming each acetate group are nearly perpendicular to the mean plane of the anthra[1,2-d]imidazole system, as indicated by the dihedral angles between them of 79.94 (9) and 85.90 (9)°. The crystal packing displays non-classical C-H...O hydrogen bonds.

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The mol­ecule of the title compound, C29H20N2O3, contains four fused rings, three are six-membered rings and one is the five-membered imidazole ring. The fused-ring system is linked to two benzyl groups. The four fused rings are folded around the O=C...C=O direction of the anthraquinone, with a dihedral angle of 16.36 (8)° between the two terminal rings (A and D). The imidazole ring (D) is almost perpendicular to the two benzyl groups (E and F) with dihedral angles of 86.69 (17) and 83.15 (13)°, respectively. In the crystal, adjacent mol­ecules are linked by inter­molecular C-H...O hydrogen bonding.

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In the title compound, C21H12N2O3, the fused-ring system is roughly planar, the largest deviation from the mean plane being 0.084 (2) Å. The two prop-2-yn-1-yl groups are almost perpendicular to the fused ring plane, making C-C-N-C torsion angles of -103.4 (2) and -105.3 (2)°, and point in opposite directions with respect to the plane. In the crystal, mol­ecules are linked by weak C-H...O hydrogen bonds, forming a three-dimensional network.

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The mol­ecular structure of the title compound, C28H20N4O6, consists of three fused six-membered rings (A,B,C) and one five-membered ring (D). The latter is linked to an isoxazole ring (E) via a methyl­ene unit. A 4-nitro-phenyl substituent (F) is attached to the isoxazole. The fused five and six-membered rings (C,D) are almost coplanar with an r.m.s. deviation of 0.0345 Å and make a dihedral angle of 9.40 (8)° with ring A. The isoxazole and 4-nitro-phenyl rings (E,F) are also almost coplanar with the imidazole and the fused adjacent ring (C,D), forming a dihedral angle of 11.4 (6)°. The crystal packing displays inter­molecular C-H...O hydrogen bonding. An intra­molecular C-H...O inter­action also occurs.

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Two isomers were isolated during the reaction between 3-methyl­quinoxalin-2-one and bis­(2-chloro­ethyl)amine hydro­chloride. The crystal structure of one isomer has already been reported [Caleb, Bouhfid, Essassi & El Ammari (2009). Acta Cryst. E65, o2024-o2025], while that of the second isomer is the subject of this work. The title compound, C14H15N3O3, has a new structure containing oxazolidine and quinoxaline rings linked by an eth­oxy group. The main difference between the two isomers is the position of the oxazolidine group with respect to the quinoxaline system. The dihedral angle between the fused planar rings and the oxazolidin-2-one ring is 41.63 (8)° in the title mol­ecule.

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The title compound is built up from a four-membered ring to which a six- and a five-membered ring are fused. In the crystal, mol­ecules are linked by N—H...O hydrogen bonds, forming chains propagating along the b-axis direction.

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The title compound is built up from two fused phenyl rings. The naphthalene ring system is approximately planar.

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The asymmetric unit of the title compound, [Zn(HPO4)(C2H3N3)]n, contains one Zn2+ cation, one (HPO4)2- anion and a 1,2,4 triazole ligand. The Zn2+ cation is coordinated in a quite regular tetra­hedral geometry by O atoms from three phosphate groups and a tertiary N atom from the triazole ring. Each phosphate anion is connected to three ZnII cations, leading to a series of corrugated organic-inorganic layers parallel to the ac plane. The overall structure involves stacking of complex hybrid organic-inorganic layers along the b axis. Cohesion in the crystal is ensured by an infinite three-dimensional network of N-H...O and O-H...O hydrogen bonds between the phosphate groups and the triazole ligands.

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In the title compound, C28H27NO3, the cyclo­hexa­none and isoxazole rings have envelope conformations, with the methyl­ene and spiro C atoms as the flaps, respectively. The mean plane of the isoxazole ring is inclined slightly to the p-tolyl ring, making a dihedral angle of 14.20 (9)°, and is nearly perpendicular to the mean plane through the tetra­lone moiety and to the meth­oxy­phenyl ring [dihedral angles = 83.41 (8) and 72.12 (9)°, respectively]. The crystal packing is stabilized mainly by van der Waals forces.

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In the title compound, C20H20O2, the exocyclic C=C double bond has an E conformation. The ethyl substituent on the cyclo­hexa­none ring is in an axial orientation. The cyclo­hexa­none ring adopts a screw-boat conformation, with the methyl­ene C atom and the C atom bearing the 4-meth­oxy­benzyl­idene group displaced from the other atoms by 0.812 (1) and 0.334 (1) Å, respectively. The dihedral angle between the planes of the benzene rings is 42.20 (8)°. In the crystal, no directional inter­actions beyond van der Waals contacts are observed.

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A new quinoline-based hydrazone compound, has been synthesized by a condensation reaction of 2-chloro-3-formyl­quinoline with phenyl­hydrazine. The quinoline ring system is essentially planar (r.m.s. deviation = 0.012 Å), and forms a dihedral angle of 8.46 (10)° with the phenyl ring substituent.

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The title compound, strontium trimanganese tris­(ortho­phosphate), was synthesized under hydro­thermal conditions. Its structure is isotypic to that of the lead analogue PbMnII2MnIII(PO4)3. Two O atoms are in general positions, whereas all others atoms are in special positions. The Sr and one P atom exhibit mm2 symmetry, the MnII atom 2/m symmetry, the MnIII atom and the other P atom .2. symmetry and two O atoms are located on mirror planes. The three-dimensional network of the crystal structure is made up of two types of chains running parallel to [010]. One chain is linear and is composed of alternating MnIIIO6 octa­hedra and PO4 tetra­hedra sharing vertices; the other chain has a zigzag arrangement and is built up from two edge-sharing MnIIO6 octa­hedra connected to PO4 tetra­hedra by edges and vertices. The two types of chains are linked through PO4 tetra­hedra, leading to the formation of channels parallel to [100] and [010] in which the SrII ions are located. They are surrounded by eight O atoms in the form of a slightly distorted bicapped trigonal prism.

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In contrast to most other structures of transition metal orthophosphates with composition M3-xM'x(PO4)2·H2O, the three metallic sites in the structure of Mn2Zn(PO4)2·H2O show no statistical disorder.

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The two orthophosphates BaMn2Fe(PO4)3 and SrMn2Fe(PO4)3 are isotypic and resemble an alluaudite-like structure. The chains characterizing the alluaudite structure are built up from edge-sharing [MnO6] and [FeO6] octa­hedra linked by PO4 tetra­hedra.

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The title compound, lead trimanganese tris(orthophosphate), has been synthesized by hydro­thermal methods. In this structure, only two O atoms are in general positions and all others atoms are in the special positions of the Imma space group. Indeed, the atoms in the Wyckoff positions are namely: Pb1 and P1 on 4e (mm2); Mn1 on 4b (2/m); Mn2 and P2 on 8g (2); O1 on 8h (m); O2 on 8i (m). The crystal structure can be viewed as a three-dimensional network of corner- and edge-sharing PO4 tetra­hedra and MnO6 octa­hedra, building two types of chains running along the b axis. The first is an infinite linear chain, formed by alternating MnIIIO6 octa­hedra and PO4 tetra­hedra which share one vertex. The second chain is built up from two adjacent edge-sharing octa­hedra (MnII2O10 dimers) whose ends are linked to two PO4 tetra­hedra by a common edge. These chains are linked together by common vertices of polyhedra in such a way as to form porous layers parallel to (001). These sheets are bonded by the first linear chains, leading to the appearance of two types of tunnels, one propagating along the a axis and the other along b. The PbII ions are located within the inter­sections of the tunnels with eight neighbouring O atoms in form of a trigonal prism that is capped by two O atoms on one side. The three-dimensional framework of this structure is compared with similar phosphates such as Ag2Co3(HPO4)(PO4)2 and Ag2Ni3(HPO4)(PO4)2.

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The mol­ecule of the title compound, C11H8N2, is approximately planar (r.m.s.deviation for all non-H atoms = 0.023 Å). The malono­nitrile C-C-C angle is 113.54 (13)°. In the crystal, mol­ecules stack head-to-tail along [010]. There are no significant inter­molecular inter­actions present.

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