Browse
Submit Data
Databases
API
Help

Dataset Information

33 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Diaqua-bis(ciprofloxacinato)manganese(II) 2,2'-bipyridine solvate tetrahydrate.

ABSTRACT: In the crystal structure of the title compound {systematic name: diaquabis-[1-cyclo-propyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydro-quinoline-3-carboxyl-ato]manganese(II) 2,2'-bi-pyridine solvate tetrahydrate}, [Mn(C(17)H(17)FN(3)O(3))(2)(H(2)O)(2)]·C(10)H(8)N(2)·4H(2)O, the pyridone O and one carboxyl-ate O atom of the two ciprofloxacin ligands are bound to the Mn(II) ion and occupy the equatorial positions, while the two aqua O atoms lie in the apical positions resulting in a distorted octa-hedral geometry. The crystal packing is stabilized by N-H?O and O-H?O hydrogen bonding interactions.

SUBMITTER: Wang YJ

PROVIDER: S-EPMC2969266 | biostudies-literature | 2009 Jun

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Diaqua-bis(ciprofloxacinato)manganese(II) 2,2'-bipyridine solvate tetrahydrate.

Wang Yan-Jun YJ Wang Na N Hu Rui-Ding RD Lin Qiu-Yue QY Wang Yun-Yun YY

Acta crystallographica. Section E, Structure reports online 20090617 Pt 7

In the crystal structure of the title compound {systematic name: diaquabis-[1-cyclo-propyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydro-quinoline-3-carboxyl-ato]manganese(II) 2,2'-bi-pyridine solvate tetrahydrate}, [Mn(C(17)H(17)FN(3)O(3))(2)(H(2)O)(2)]·C(10)H(8)N(2)·4H(2)O, the pyridone O and one carboxyl-ate O atom of the two ciprofloxacin ligands are bound to the Mn(II) ion and occupy the equatorial positions, while the two aqua O atoms lie in the apical positions resulting in a distorted oc ...[more]

PMID: 21582711

Similar Datasets

Diaqua-bis(norfloxacinato)manganese(II) 2,2'-bipyridine solvate tetra-hydrate.

Project description:In the crystal structure of the title compound {systematic name: diaqua-bis[1-ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydro-quinoline-3-carboxyl-ato]manganese(II) 2,2'-bipyridine solvate tetra-hydrate}, [Mn(C(16)H(17)FN(3)O(3))(2)(H(2)O)(2)]·C(10)H(8)N(2)·4H(2)O, the pyridone O atom and one carboxyl-ate O atom of the two norfloxacin ligands are bound to the Mn(II) ion, which is located on an inversion centre, and occupy equatorial positions, while two aqua O atoms lie in apical positions, resulting in a distorted octa-hedral geometry. The crystal packing is stabilized by N-H?O and O-H?O hydrogen-bonding interactions.

| S-EPMC2969423 | biostudies-literature

?-Oxalato-bis-[bis-(2,2'-bipyridine)-manganese(II)] bis(perchlorate) 2,2'-bipyridine solvate.

Project description:The unit cell of the title compound, [Mn(2)(C(2)O(4))(C(10)H(8)N(2))(4)](ClO(4))(2)·C(10)H(8)N(2), consists of a binuclear cation, two perchlor-ate anions, and one solvent 2,2'-bipyridine (bpy) mol-ecule. In the complex cation [Mn(2)(C(2)O(4))(C(10)N(2)H(8))(4)](2+), two Mn(II) atoms are bridged by a bis-(bidentate) oxalate ligand, each Mn(II) atom being further coordinated by two bpy ligands in a distorted octa-hedral geometry. The distance between the two six-coordinated metal atoms is 5.583?(1)?Å. ?-? stacking inter-actions [inter-planar distances between bpy rings = 3.739?(1)?Å] are essential to the supramolecular assembly. There are extensive inter-ionic C-H?O inter-actions between the cations and between the cation and anion. Three of the four perchlorate O atoms are disordered over two sets of sites with occupancy ratios of 0.852?(6):0.148?(6).

| S-EPMC3201320 | biostudies-other

Diaqua-(2,2'-bipyridine-?N,N')bis-(perchlorato-?O)copper(II).

Project description:The central CuN(2)O(4) motif of the title compound, [Cu(ClO(4))(2)(C(10)H(8)N(2))(H(2)O)(2)], exhibits a Jahn-Teller-distorted octa-hedral geometry around the metal atom, showing a considerably long Cu-O bond distance of 2.5058?(12)?Å towards the second perchlorate group, giving a (4 + 1+1)-type coordination mode. In the crystal, the components are linked via inter-molecular O-H?O hydrogen bonds, forming layers parallel to (001). Additional stabilization within these layers is provided by ?-? [centroid-centroid distances of 3.7848?(9)-4.4231?(9)?Å] stacking inter-actions.

| S-EPMC3089365 | biostudies-literature

trans-Diaqua-bis(2,2'-bipyridine-κN,N')ruthenium(II) bis-(trifluoro-methane-sulfonate).

Project description:The title compound, trans-[Ru(bpy)(2)(H(2)O)(2)](CF(3)SO(3))(2) (bpy = 2,2'-bipyridine, C(10)H(8)N(2)), crystallized from the decomposition of an aged aqueous solution of a dimeric complex of cis-Ru(bpy)(2) in 0.1 M triflic acid. The Ru(II) ion is located on a crystallographic inversion center and exhibits a distorted octa-hedral coordination with equivalent ligands trans to each other. The Ru-O distance is 2.1053 (16) Å and the Ru-N distances are 2.0727 (17) and 2.0739 (17) Å. The bpy ligands are bent, due to inter-ligand steric inter-actions between H atoms of opposite pyridyl units across the Ru center. The crystal structure exhibits an extensive hydrogen-bonding network involving the water ligands and the trifluoromethane-sulfonate counter-ions within two-dimensional layers, although no close hydrogen-bond inter-actions exist between different layers.

| S-EPMC2959720 | biostudies-literature

Bis(2,2'-bipyridine N,N'-dioxide)bis-(tri-cyano-methanido)manganese(II).

Project description:In the title complex, [Mn(C(4)N(3))(2)(C(10)H(8)N(2)O(2))(2)], the Mn(II) atom lies on an inversion center and is coordinated by two 2,2'-bipyridine N,N'-dioxide (dpdo) mol-ecules and two tricyano-methanide (tcm) ligands to form a distorted octa-hedral geometry. Weak inter-molecular C-H⋯O or C-H⋯N hydrogen bonds, involving either the O atom of the dpdo mol-ecule and the pyridyl H atom, or the N atom of the tcm anion and the pyridyl H atom, result in the formation of a three-dimensional network structure.

| S-EPMC2977596 | biostudies-literature

Bis(μ-carboxyl-atoethyl-phospho-nato)bis-[aqua-(2,2'-bipyridine)manganese(II)].

Project description:The title compound, [Mn(2)(HO(3)PCH(2)CH(2)COO)(2)(C(8)H(8)N(2))(2)(H(2)O)(2)], was obtained by hydro-thermal synthesis. The manganese(II) ions are six-coordinate and are linked by two 2-carboxy-ethyl-phospho-nate ligands, forming a centrosymmetric dimer. The Mn ions adopts a distorted octahedral coordination geometry. The dimers are further linked by O-H⋯O hydrogen bonds and π-π stacking inter-actions [centroid-centroid distance 4.2754 (4) Å].

| S-EPMC2915102 | biostudies-literature

catena-Poly[[diaqua-bis(thio-cyanato-?N)cobalt(II)]-?-4,4'-bipyridine-?N:N'] 4,4'-bipyridine solvate].

Project description:In the title complex, {[Co(NCS)(2)(C(10)H(8)N(2))(H(2)O)(2)]·C(10)H(8)N(2)}(n), the Co(II) ion is located on an inversion centre and is coordinated by two N atoms from the two 4,4'-bipyridine ligands, two O atoms from the water mol-ecule, and two N atoms from two isothio-cyanate ions in a distorted octa-hedral environment. In the crystal, the coordinated water mol-ecules, isothio-cyanate ions and solvent 4,4'-bipyridine mol-ecules are linked by O-H?S and O-H?N hydrogen bonds into layers parallel to the ab plane.

| S-EPMC2969491 | biostudies-literature

Diaqua-bis(1,3-propane-diamine)nickel(II) squarate tetrahydrate.

Project description:The asymmetric unit of the title compound, [Ni(C(3)H(10)N(2))(2)(H(2)O)(2)](C(4)O(4))·4H(2)O, contains one-half of the diaqua-bis(1,3-propane-diamine)nickel(II) cation, one-half of the centrosymmetric squarate anion and two uncoordinated water mol-ecules. In the cation, the Ni(II) atom is located on a crystallographic inversion centre and has a slightly distorted octa-hedral coordination geometry. The six-membered chelate ring adopts a chair conformation. O-H?O hydrogen bonds link the cation and anion through the water mol-ecule, while N-H?O hydrogen bonds link the cation and anion and cation and water mol-ecules. In the crystal structure, inter-molecular O-H?O and N-H?O hydrogen bonds link the mol-ecules into a three-dimensional network structure.

| S-EPMC2969320 | biostudies-literature

Bis(2,2'-bipyridine)(5-isothio-cyanato-1,10-phenanthroline)ruthenium(II) bis-(hexa-fluoridophosphate) acetonitrile solvate.

Project description:The title compound, [Ru(C(10)H(8)N(2))(2)(C(13)H(7)N(3)S)](PF(6))(2)·CH(3)CN, was synthesized by the reaction of thio-phosgene and bis-(2,2'-bipyridine)(1,10-phenanthrolin-5-amine)ruthenium(II) bis-(hexa-fluoridophosphate). The Ru(II) atom adopts a slightly distorted octa-hedral RuN(6) coordinaton formed by four N atoms of two bipyridine ligands and by two N atoms of the 1,10-phenantroline ligand. The isothio-cyanate group is almost linear, with an N-C-S angle of 174.4?(6)°. Two of the three hexa-fluoridophosphate counter-anions are located on inversion centres.

| S-EPMC2970250 | biostudies-literature

Diaqua-bis-(4,4'-bipyridine-?N)bis-(2,4,5-trifluoro-3-hy-droxy-benzoato-?O)manganese(II).

Project description:In the title compound, [Mn(C(7)H(2)F(3)O(3))(2)(C(10)H(8)N(2))(2)(H(2)O)(2)], the Mn(II) ion, situated on a centre of inversion, has a distorted octa-hedral coordination geometry and is coordinated by two N atoms from two 4,4'-bipyridine ligands, two O atoms from two 2,4,5-trifluoro-3-hy-droxy-benzoate ligands and two water mol-ecules. Inter-molecular O-H?N hydrogen bonds link the mol-ecules into a chain along the a axis. Inter-actions between neighboring chains occur through O-H?O hydrogen bonds, which link the chains into a two-dimensional supra-molecular network parallel to the ac plane. In addition, O-H?O hydrogen bonds between the water mol-ecules and carboxyl-ate groups also exist in the the crystal structure.

| S-EPMC3238726 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data