Browse
Submit Data
Databases
API
Help

Dataset Information

23 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

(1-Ferrocenyl-4,4,4-trifluoro-butane-1,3-dionato-?O,O)bis-(triphenyl-phosphane)copper(I).

ABSTRACT: In the title mononuclear coordination complex, [CuFe(C(5)H(5))(C(9)H(5)F(3)O(2))(C(18)H(15)P)(2)], the Cu(I) ion is coordinated by the chelating ?-diketonate 1-ferrocenyl-4,4,4-trifluoro-butane-1,3-dione ligand through two O atoms and the two datively bonded triphenyl-phosphane ligands resulting in a distorted tetra-hedral coordination sphere. The Cu(I) ion, together with its chelating butane-1,3-dione group, is mutually coplanar [greatest displacement of an atom from this plane = 0.037?(1)?Å], and the Cu(I) ion lies slightly above [0.013?(1)?Å] the plane. The overall geometry, including the bond distances and angles within the complex, corresponds to those of other reported copper(I) ?-diketon-ates featuring organic groups at the ?-diketonate ligand.

SUBMITTER: Ruffer T

PROVIDER: S-EPMC3051674 | biostudies-literature | 2011 Jan

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

(1-Ferrocenyl-4,4,4-trifluoro-butane-1,3-dionato-κO,O)bis-(triphenyl-phosphane)copper(I).

Rüffer Tobias T Joubert Chris C CC Buitendach Blenerhassit E BE Swarts Jannie C JC Jakob Alexander A Lang Heinrich H

Acta crystallographica. Section E, Structure reports online 20110122 Pt 2

In the title mononuclear coordination complex, [CuFe(C(5)H(5))(C(9)H(5)F(3)O(2))(C(18)H(15)P)(2)], the Cu(I) ion is coordinated by the chelating β-diketonate 1-ferrocenyl-4,4,4-trifluoro-butane-1,3-dione ligand through two O atoms and the two datively bonded triphenyl-phosphane ligands resulting in a distorted tetra-hedral coordination sphere. The Cu(I) ion, together with its chelating butane-1,3-dione group, is mutually coplanar [greatest displacement of an atom from this plane = 0.037 (1) Å], ...[more]

PMID: 21522889

Similar Datasets

Bis(pyridine-κN)bis-[4,4,4-trifluoro-1-(4-fluoro-phen-yl)butane-1,3-dionato-κO,O']cobalt(II).

Project description:In the structure of the title compound, [Co(C(10)H(5)F(4)O(2))(2)(C(5)H(5)N)(2)], cobalt(II) forms a complex with two 4,4,4-trifluoro-1-(4-fluoro-phen-yl)butane-1,3-dionate anions and two pyridine mol-ecules in an octa-hedral coordination environment, where the two dionate ligands are in equatorial positions and the two pyridine mol-ecules in axial positions. The complex is located on a crystallographic inversion centre.

| S-EPMC2960175 | biostudies-literature

Tris[4,4,4-trifluoro-1-(2-thien-yl)butane-1,3-dionato]aluminium(III)-tris-[4,4,4-trifluoro-1-(2-thien-yl)butane-1,3-dion-ato]iron(III) (3/1).

Project description:In the title compound, [Al(C(8)H(4)F(3)O(2)S)(3)](3)[Fe(C(8)H(4)F(3)O(2)S)(3)], the metal centre is statistically occupied by Al(III) and Fe(III) cations in a 3:1 ratio. The metal centre is within an octa-hedral O(6) donor set defined by three chelating substituted acetoacetonate anions. The ligands are arranged around the periphery of the mol-ecule with a mer geometry of the S atoms.

| S-EPMC2977190 | biostudies-literature

Potassium bis-(1,1,1,5,5,5-hexa-fluoro-pentane-2,4-dionato)bis-(4,4,4-trifluoro-1-phenyl-butane-1,3-dionato)europate(III).

Project description:In the crystal structure of the title complex, K[Eu(C(5)HF(6)O(2))(2)(C(10)H(6)F(3)O(2))(2)], the Eu(III) ion is in a slightly distorted square-anti-prismatic coordination geometry which is defined by eight O atoms of the anionic ?-diketone ligands. The two K(+) ions lie on crystallographic inversion centers. The Eu-O bond distances are in the range 2.294?(5)-2.413?(5)?Å. The crystal used was a non-merohedral twin, the ratio of the twin domains being 0.5236?(5):0.4764?(5).

| S-EPMC3006768 | biostudies-literature

(N,N-Diethyl-nicotinamide-?N)bis-[4,4,4-trifluoro-1-(thien-2-yl)butane-1,3-dionato-?O,O']copper(II).

Project description:In the title compound, [Cu(C(8)H(4)F(3)O(2)S)(2)(C(10)H(14)N(2)O)], the Cu(II) atom exists in a distorted CuNO(4) square-pyramidal geometry; the metal atom lies above a square plane defined by four O atoms of the two chelating anionic ligands, displaced in the direction of the axial occupant, the pyridine N atom, by 0.179?(1)?Å. Weak inter-molecular C-H?O and C-H?F hydrogen bonding is present in the crystal structure. One thienyl ring is disordered over two orientations in an occupancy ratio of 0.69?(1):0.31.

| S-EPMC3120436 | biostudies-other

Propyl-ammonium 4,4,4-trifluoro-1-(naphthalen-2-yl)butane-1,3-dionate.

Project description:The title salt, C(3)H(10)N(+)·C(14)H(8)F(3)O(2) (-), constitutes the first organic crystal containing a residue of 4,4,4-trifluoro-1-(naphthalen-2-yl)butane-1,3-dione. The terminal -CF(3) group is disordered over two locations [occupancy ratio = 0.830 (7):0.170 (7)]. Bond delocalization involving the two carbonyl groups and the α-carbon was observed. The crystal packing is mediated by several supra-molecular inter-actions, namely charged-assisted N-H⋯O hydrogen bonds, C-H⋯F and C-F⋯F short contacts and C-H⋯π inter-actions.

| S-EPMC3239027 | biostudies-literature

Poly[μ2-aqua-μ4-[1-(4-chloro-phen-yl)-4,4,4-tri-fluoro-butane-1,3-dionato]-potassium].

Project description:In the title compound, [K(C10H5ClO2F3)(H2O)] n , the two independent K(+) ions are located on a twofold rotation axis. For each of the cations, the distorted cubic coordination environment is defined by two F and four O atoms of symmetry-related 1,4-chloro-phenyl-4,4,4-tri-fluoro-butane-1,3-dionate anions and by two O atoms of water mol-ecules. The μ4-bridging character of the anion and the μ2-bridging of the water mol-ecule lead to the formation of layers parallel to (100). The coordinating water mol-ecules are also involved in O-H⋯O hydrogen bonds that reinforce the mol-ecular cohesion within the layers, which are stacked along [100]. The β-diketonate anion is not planar, with an angle of 31.78 (10)° between the mean planes of the diketonate group and the chloro-phenyl ring.

| S-EPMC3772444 | biostudies-literature

Bis-(ethanol-κO)bis(1-ferrocenyl-4,4,4-tri-fluoro-butane-1,3-dionato-κ2 O,O')nickel(II).

Project description:In the title compound, [NiFe2(C5H5)(C9H5F3O2)2(C2H6O)2], the central NiII ion is observed in an octa-hedral coordination environment. The chelating β-diketonate ligands are substituted by ferrocene, a lipophilic organometallic moiety. The ferrocene groups have the normal geometry, with eclipsed cyclo-penta-diene rings. Coordinated ethanol mol-ecules are engaged in inter-molecular hydrogen bonds, and the crystal is further stabilized by weak C-H⋯F and C-H⋯π contacts.

| S-EPMC9462358 | biostudies-literature

Bis{1-[4-(benz-yloxy)phen-yl]-4,4,4-tri-fluoro-butane-1,3-dionato(1-)}dipyri-dine-cobalt(II).

Project description:In the title compound, [Co(C(17)H(12)F(3)O(3))(2)(C(5)H(5)N)(2)], the Co(II) ion is situated on a twofold rotation axis, coordinated by four O atoms from two 1-[4-(benz-yloxy)phen-yl]-4,4,4-trifluoro-butane-1,3-dionate(1-) (L) ligands and two N atoms from two pyridine ligands in a distorted octa-hedral geometry. The two pyridine rings form a dihedral angle of 84.63?(7)°. The two benzene rings in L are twisted at 58.83?(5)°. Weak inter-molecular C-H?F hydrogen bonds consolidate the crystal packing.

| S-EPMC3247528 | biostudies-literature

catena-Poly[[(triphenyl-phosphane-?P)copper(I)]-di-?-bromido-[(triphenyl-phos-phane-?P)copper(I)]-?-1,3-bis(pyridin-4-yl)-propane-?N:N'].

Project description:Through a diffusion reaction, cuprous bromide, triphenyl-phosphane and 1,3-bis-(pyridin-4-yl)propane (bpp) were self-assembled to form the one-dimensional title compound, [Cu(2)Br(2)(C(13)H(14)N(2))(C(18)H(15)P)(2)](n). Each Cu(I) atom is coordinated by two Br atoms, one P atom from a triphenyl-phosphane ligand and one N atom from a bpp mol-ecule in a distorted tetra-hedral geometry. Two ?(2)-Br bridges connect two [Cu(PPh(3))](+) units to form neutral [CuBr(PPh(3))](2) dimers, which are linked by the flexible bridging bpp ligands to form a one-dimensional chain structure parallel to the c axis. The dihedral angle between the pyridine rings of the bpp ligand is 34.59?(14)°.

| S-EPMC3297220 | biostudies-literature

Tetra-kis(triphenyl-phosphane-?P)silver(I) trifluoro-acetate ethanol monosolvate.

Project description:In the title solvated salt, [Ag(C18H15P)4](CF3CO2)·C2H5OH, the Ag(I) atom is coordinated by four P atoms from triphenyl-phosphane ligands in a distorted tetra-hedral geometry. The anion and solvent are engaged in weak O-H?O hydrogen bonds. Of the four triphenyl-phosphane ligands, two each have an equally disordered phenyl ring while the Ag(I) atom is disordered over two positions in a 0.9595?(15):0.0405?(15) ratio and the trifluoro-acetate anion is equally disordered over two positions with respect to the lattice ethanol mol-ecule.

| S-EPMC3588779 | 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