ABSTRACT
In the title compound, C(12)H(18)NO(+)·PF(6) (-), the asymmetric unit consists of two cation-anion pairs. The six F atoms of one anion are disordered over two sets of sites in a 0.592â (6):0.408â (6) ratio. The morpholinium rings adopt chair conformations.
ABSTRACT
In the title compound, C(23)H(25)NO(5), the pyran ring adopts a flattened boat conformation, while the two cyclo-hexenone rings are in envelope conformations. The 3-nitro-phenyl ring is almost perpendicular to the pyran ring, making a dihedral angle of 87.1â (3)°.
ABSTRACT
The title compound, C(25)H(22)O(2), was synthesized via the three-component coupling of benzaldehyde, 2-naphthol and 5,5-dimethyl-cyclo-hexane-1,3-dione. In the crystal structure, centrosymmetrically related mol-ecules are linked into dimers by pairs of inter-molecular C-Hâ¯O hydrogen bonds. The dimers are further connected into a three-dimensional network by π-π aromatic stacking inter-actions involving the naphthalene ring system, with centroid-centroid separations of 3.695â (7)â Å.
ABSTRACT
In the title complex, [Ni(H(2)O)(6)](C(6)H(10)N(2)O(6)PS)(2) x 6 H(2)O, the asymmetric unit consists of one-half of an Ni atom (which lies on an inversion centre) with three coordinated water molecules, one complete 2-carboxylato-2-(isothiouronium-S-ylmethyl)propane-1,3-diyl phosphate anion and three noncoordinated water molecules. The hexaaquanickel(II) cations have distorted octahedral coordination and are connected via water chains to form two-dimensional supramolecular networks parallel to the ab plane. The phosphate ester anion is linked via N-H...O and O-H...O hydrogen bonds, thus creating various ring, dimer and chain hydrogen-bonding patterns, and building up a second two-dimensional supramolecular network parallel to the ab plane. The crystal structure is further stabilized by an intra- and interlayer hydrogen-bond network. This work illustrates that a carboxylate with a caged phosphate ester can open its ring in the presence of dichloridotetrakis(thiourea)nickel, and the resulting polyfunctional anion can be used for constructing a complex hydrogen-bonding scheme.
ABSTRACT
The asymmetric unit of the title complex, {[Cu(C(5)H(6)O(6)P)(2)(H(2)O)(2)] x 2 H(2)O}(n), consists of half a Cu atom, one complete 1-oxo-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane-4-carboxylate anion ligand and two non-equivalent water molecules. The Cu atom lies on a crystallographic inversion centre and has an elongated axially distorted octahedral environment. A two-dimensional layer structure parallel to (100) is formed as a result of the connectivity brought about by each anion bonding to two different Cu atoms via a carboxylate O atom and a bridging O atom of a C-O-P group. The water molecules participate in extensive O-H...O hydrogen bonding. Neighbouring layers are linked together by intermolecular hydrogen-bonding interactions. The crystal structure is characterized by intra- and interlayer motifs of a hydrogen-bonded network. This study demonstrates the usefulness of carboxylates with caged phosphate esters in crystal engineering.
ABSTRACT
In the title molecular salt, C(9)H(18)NO(+)·Cl(-), the morpholine ring adopts a chair conformation. In the crystal structure, intra-molecular C-Hâ¯Cl bonds occur and inter-molecular C-Hâ¯O and C-Hâ¯Cl hydrogen bonds link the mol-ecules.
ABSTRACT
In the mol-ecule of the title compound, C(17)H(18)N(2)O(2), the dihedral angle between the aromatic rings is 74.26â (3)°. The oxime units are oriented at dihedral angles of 7.66â (3) and 33.06â (3)° with respect to the adjacent rings, and they have E configurations about the C=N bonds.
