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In the title binuclear copper(II) complex, [Cu2(ClO4)2(OH)2(C10H8N2)2], the CuII ion is coordinated in the form of a Jahn–Teller distorted octahedron by two bipyridine N atoms, two perchlorate O atoms and two hydroxide O atoms, and displays a distorted octahedral geometry. The molecule belongs to the symmetry point group C2h. The CuII ion is located on a twofold rotation axis and the hydroxide and perchlorate ligands are located on a mirror plane. Within the dinuclear molecule, the Cu
Cu separation is 2.8614 (7) Å. The crystal structure exhibits O—HO, C—HO and π–π [centroid–centroid distance = 3.5374 (13) Å] interactions.
Cu separation is 2.8614 (7) Å. The crystal structure exhibits O—HO, C—HO and π–π [centroid–centroid distance = 3.5374 (13) Å] interactions.organic compoundsOpen access
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In the title compound, C33H26N2O4, the pyrazole ring makes dihedral angles of 15.13 (7) and 60.80 (7)° with the adjacent phenyl rings. Both dihydropyran rings exhibit half-chair conformations. A weak intramolecular C—HO interaction occurs. In the crystal, molecules are linked into inversion dimers through pairs of C—HN interactions. Weak C—Hπ interactions are also observed.
O interaction occurs. In the crystal, molecules are linked into inversion dimers through pairs of C—HN interactions. Weak C—Hπ interactions are also observed.organic compoundsOpen access
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The title compound C28H22O2, basically consists of three ring systems, viz. a central benzene ring, with a lateral napthalene group to which it subtends a dihedral angle of 66.56 (4)° and a tetrahydropyran ring exhibiting a half-chair conformation. The molecular structure is stabilized by a weak intramolecular C—HO interaction, while the crystal packing features weak C—Hπ contacts.
O interaction, while the crystal packing features weak C—Hπ contacts.organic compoundsOpen access
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In the title compound, C20H19NO2, the dihedral angle between the benzene rings is 77.12 (8)°. The terminal isopropyl group is disordered over two orientations, with site occupancies of 0.720 (14) and 0.280 (14). In the crystal, molecules are linked through a weak C—HO interaction, forming a zigzag chain along the c-axis direction.
O interaction, forming a zigzag chain along the c-axis direction.organic compoundsOpen access
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The title compound C11H10BrN, has an E conformation at the C=C bond of the acrylonitrile unit. The vinyl group makes a dihedral angle of 44.53 (12)° with the benzene ring. In the crystal, weak C—Hπ interactions involving the benzene ring are observed.
π interactions involving the benzene ring are observed.organic compoundsOpen access
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The molecular structure of the title compound, C16H16N2O2, is stabilized by intramolecular O—HN hydrogen bonds with S(6) graph-set motifs, so that the molecule is almost planar, with a C=N—N=C torsion angle of −179.7 (2)° and a dihedral angle of 1.82 (12)° between the aromatic rings. In the crystal, weak C—Hπ interactions lead to the formation of a three-dimensional network.
N hydrogen bonds with S(6) graph-set motifs, so that the molecule is almost planar, with a C=N—N=C torsion angle of −179.7 (2)° and a dihedral angle of 1.82 (12)° between the aromatic rings. In the crystal, weak C—Hπ interactions lead to the formation of a three-dimensional network.organic compoundsOpen access
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In the title compound, C22H16ClNO, the quinoline ring system makes dihedral angles of 56.30 (6) and 7.93 (6)°, respectively, with the adjacent phenyl and benzene rings. The dihedral angle between these phenyl and benzene rings is 56.97 (8)°. In the crystal, weak C—Hπ and π–π [centroid–centroid distances of 3.7699 (9) and 3.8390 (9) Å] interactions link the molecules into a layer parallel to the ab plane.
π and π–π [centroid–centroid distances of 3.7699 (9) and 3.8390 (9) Å] interactions link the molecules into a layer parallel to the ab plane.organic compoundsOpen access
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In the title compound, C25H21BrN2O2, the fused isoxazolidine ring adopts an envelope conformation with the N atom at the flap and the mean plane of the ring makes dihedral angles of 54.37 (12) and 87.32 (13)°, respectively, with the adjacent phenyl and benzene rings. The tetrahydropyran ring has a half-chair conformation. In the crystal, molecules are linked into a double-column structure along the b-axis direction through weak C—HO and C—Hπ interactions.
O and C—Hπ interactions.organic compoundsOpen access
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In the title compound, C28H23N3O2, the pyrazole ring makes a dihedral angle of 16.90 (6)° with the phenyl ring to which it is attached. Both dihydropyran rings exhibit half-chair conformations. Intramolecular C—HO interactions generate S(6) and S(8) ring motifs. In the crystal, weak C—HO and C—Hπ interactions occur.
O interactions generate S(6) and S(8) ring motifs. In the crystal, weak C—HO and C—Hπ interactions occur.
