Preparation and Structural Characterization of Cyanatocopper(II) Complexes with Substituted Piperidines

1992 ◽  
Vol 57 (9) ◽  
pp. 1899-1904
Author(s):  
Anna Mašlejová ◽  
Mária Hvastijová ◽  
Jiří Kohout
Keyword(s):  
Structural Characterization ◽  
Room Temperature ◽  
Magnetic Moments ◽  
Esr Spectra ◽  
Complex Compounds ◽  
Coordination Geometry ◽  
Prepared Complex ◽  
Axial Interaction

Coordination geometry of the newly prepared complex compounds of [Cu(NCO)2L2] type (L is piperidine, 2-methylpiperidine, 4-methylpiperidine and 2,6-dimethylpiperidine) was investigated at room temperature utilizing the results of infrared, electronic and ESR spectra and magnetic moments. All complexes show a tetragonal arrangement with small axial interaction depending on steric properties of the piperidine ligand given.

Structural Systematics of Rare Earth Complexes. VII. Crystal Structure of Bis(2,2'/6',2␛-Terpyridinium) Octaaquaterbium(III) Heptachloride Hydrate

1994 ◽  
Vol 47 (2) ◽  
pp. 391 ◽  
Author(s):  
CJ Kepert ◽  
BW Skeleton ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Rare Earth ◽  
Single Crystal ◽  
Structural Characterization ◽  
Title Compound ◽  
Room Temperature ◽  
Chloride Ions ◽  
Full Matrix ◽  
X Ray

The room-temperature single-crystal X-ray structural characterization of the title compound (tpyH2)2[Tb(OH2)8]Cl7.~2⅓H2O is recorded. Crystals are triclinic, Pī , a 17.063(5), b 16.243(3), c 7.878(3) Ǻ, α 84.78(2), β 84.39(3), γ 87.81(2)°, Z = 2 formula units; 3167 'observed' diffractometer reflections were refined by full-matrix least-squares procedures to a residual of 0.057. Notable features of interest of the compound are the 'chelation' of chloride ions by the terpyridinium cations , and the existence of a free [Tb(OH2)8]2+ cation in the presence of an abundance of chloride ions.

Structural Characterization of a Cage Ligand Fragmentation Reaction

1994 ◽  
Vol 47 (1) ◽  
pp. 181 ◽  
Author(s):  
JM Harrowfield ◽  
AM Sargeson ◽  
BW Skelton ◽  
AH White
Keyword(s):  
Single Crystal ◽  
Structural Characterization ◽  
Room Temperature ◽  
Fragmentation Reaction ◽  
X Ray ◽  
Nitrogen Donor ◽  
Crystal Structural

The room temperature X-ray single-crystal structural characterization of a protonated copper(II) complex of a ligand artefact, L′, of L = N-Me6sar (described in an accompanying paper) is recorded, the new ligand L′ being generated formally by elimination of a CH2CH2 bridge between a pair of nitrogen donor atoms of L. The complex, [ ClCu (H2L′) (ClO4)3.2H2O, is orthorhombic, Pccn , a 22.528(7), b 10.544(3), c 13.748(6) Ǻ, Z = 4 formula units, R being 0.053 for 1133 independent 'observed' [I > 3σ(I)] reflections. The cation, containing five-coordinate square-pyramidal ClCuN4 copper, is disposed with the Cu- Cl bond [2.458(3)Ǻ] lying on a crystallographic 2 axis; Cu-N distances are 2.094(8) and 2.093(8)Ǻ.

Spectroscopic, thermal, magnetic and structural characterization of K3VF6 prepared at room temperature

Polyhedron ◽  
2011 ◽  
Vol 30 (8) ◽  
pp. 1425-1429 ◽  
Author(s):  
R. Nagarajan ◽  
Neetu Tyagi ◽  
Samuel Lofland ◽  
K.V. Ramanujachary
Keyword(s):  
Structural Characterization ◽  
Room Temperature

Disorder at the Chiral Cα Center and Room-Temperature Solid-State cis–trans Isomerization; Synthesis and Structural Characterization of Copper(II) Complexes with d-allo,l-Isoleucine

2018 ◽  
Vol 18 (9) ◽  
pp. 5138-5154 ◽  
Author(s):  
Jelena Pejić ◽  
Darko Vušak ◽  
Gábor Szalontai ◽  
Biserka Prugovečki ◽  
Draginja Mrvoš-Sermek ◽  
...  
Keyword(s):  
Solid State ◽  
Structural Characterization ◽  
Room Temperature ◽  
Trans Isomerization

Single Crystal X-Ray Structural Characterization of [BiX2(S2CNEt2)]Infinity∞, X=Cl, Br

1994 ◽  
Vol 47 (2) ◽  
pp. 405 ◽  
Author(s):  
PK Bharadwaj ◽  
AM Lee ◽  
BW Skelton ◽  
BR Srinivasan ◽  
AH White
Keyword(s):  
Single Crystal ◽  
Sulfur Atom ◽  
Structural Characterization ◽  
Structure Determination ◽  
Room Temperature ◽  
X Ray ◽  
Structure Determinations

Single-crystal room-temperature X-ray structure determinations of the title compounds have been carried out. The two compounds are isomorphous, and isomorphous with the previously determined iodide analogue, being monoclinic, P 21/c, a ≈ 10.0, b ≈ 14.9, c ≈ 7.8 Ǻ, β ≈ 92°, Z = 4 formula units; residuals were 0.037, 0.036 for 2197, 1654 'observed' reflections for X = Cl , Br respectively. As in the iodide, the complexes are infinite polymers, with successive bismuth atoms bridged by the two halides and one sulfur atom of the ligand , which also chelates each bismuth. The structure determination of C5H5NCONEt2]2 [Cl5Bi(NC5H5)], isostructural with its thiocarbamoyl analogue, is also recorded.

Rare earth-rhodium-plumbides RE2Rh2Pb with RE = La–Nd, Sm, Gd and Tb

2018 ◽  
Vol 73 (12) ◽  
pp. 1015-1021 ◽  
Author(s):  
Lukas Heletta ◽  
Rainer Pöttgen
Keyword(s):  
Room Temperature ◽  
Magnetic Moments ◽  
Induction Melting ◽  
Temperature Dependent ◽  
X Ray ◽  
Conduction Electrons ◽  
Paramagnetic Behavior ◽  
Arc Melting ◽  
Intergrowth Structures

AbstractThe plumbides RE2Rh2Pb (RE = La–Nd, Sm, Gd, Tb) were synthesized in sealed niobium ampoules by induction melting of the pure elements or directly via arc-melting. The characterization of the samples by X-ray powder diffraction confirmed their Mo2B2Fe-type structure (space group P4/mbm) at room temperature. The Sm2Rh1.924Pb structure was refined from single-crystal X-ray diffractometer data: a=760.02(5), c=378.20(3) pm, wR=0.0387, 292 F2 values, 13 variables. The rhodium site shows small defects. The RE2Rh2Pb plumbides are simple 1:1 intergrowth structures of AlB2 and CsCl related slabs of compositions RERh2 and REPb. The Rh2 dumbbell in the SmRh2 slab of Sm2Rh2Pb shows a Rh–Rh distance of 281 pm. Temperature-dependent magnetic susceptibility measurements of La2Rh2Pb, Pr2Rh2Pb and Nd2Rh2Pb showed that the rhodium atoms carry no localized magnetic moments. La2Rh2Pb exhibits Pauli-paramagnetic behavior induced by the conduction electrons. The ground state of the praseodymium compound is ferromagnetic below TC=3.3 K while the neodymium compound shows a transition to an antiferromagnetic state at TN=6.1 K and a metamagnetic transition at a critical field of ca. 1000 Oe.

Metal Ion Binding to Calixarenes: Pendent Arm Coordination Assisted by Self-Inclusion

1994 ◽  
Vol 47 (6) ◽  
pp. 1185 ◽  
Author(s):  
JM Harrowfield ◽  
M Mocerino ◽  
BW Skelton ◽  
CR Whitaker ◽  
AH White
Keyword(s):  
Structural Characterization ◽  
Metal Ion ◽  
Room Temperature ◽  
Ion Binding ◽  
Metal Ion Binding ◽  
Cone Conformation ◽  
X Ray ◽  
Partial Cone ◽  
Arm Coordination

The synthesis and room-temperature single-crystal X-ray structural characterization of 25,27- di(allyloxy)-5,17-di-t-butyl-26,28-dimethoxycalix[4]arene are recorded. Crystals are monoclinic, C2/c, a 29.089(5), b 10.742(2), c 26.218(8) Ǻ, β 110.09(2)°, Z = 8; the structure was refined to a residual of 0.065 for 4103 independent 'observed' [I > 3σ(I)] reflections. The flattened partial cone conformation of the molecule allows inclusion of one of the methoxy substituents in a way which could block inclusion of a metal ion capable of polyhapto aromatic coordination and which may therefore explain why solution n.m.r. measurements indicate that silver(I) binds to the pendent alkene groups.

Sign in / Sign up

Export Citation Format

Share Document