Crystal structure of Bis(tri-2-pyridylamine)cobalt(II) diperchlorate

1978 ◽  
Vol 31 (12) ◽  
pp. 2647 ◽  
Author(s):  
ES Kucharski ◽  
WR McWhinnie ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Least Squares ◽  
High Spin ◽  
Metal Atom ◽  
Title Compound ◽  
Coordination Geometry ◽  
X Ray Diffraction ◽  
X Ray ◽  
The One

The crystal structure of the title compound, [Co((C5H4N)3N)2] (ClO4)2, has been determined by single-crystal X-ray diffraction at 295(1) K, i.e. in its pseudo-'high-spin' form, and refined by least squares to a residual of 0.061 for 4639 'observed' reflections. Crystals are monoclinic, P21/a, a 12.811(7), b 17.644(7), c 8.375(4) Ǻ, β 120.15(3)°, Z 2. Whereas in the iron(II) ('low-spin') analogue, the metal atom coordination geometry deviates only trivially from octahedral (<Fe-N> 1.982 Ǻ, <N-Fe-N> within the one ligand 88.1°), in the present compound Co-N ranges from 2.100(2) to 2.152(2) Ǻ and the intraligand N-Co-N angles range from 84.86(7) to 86.09(8)°.

Crystal structure of Bis(tri-2-pyridylamine)iron(II) diperchlorate

1978 ◽  
Vol 31 (1) ◽  
pp. 53 ◽  
Author(s):  
ES Kucharski ◽  
WR McWhinnie ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Least Squares ◽  
Metal Atom ◽  
Title Compound ◽  
Complex Cation ◽  
X Ray Diffraction ◽  
Tridentate Ligands ◽  
X Ray ◽  
The One

The crystal structure of the title compound, [Fe((C5H4N)3N)2] (ClO4)2, has been determined by single-crystal X-ray diffraction at 295 K and refined by least squares to a residual of 0.059 (1995 'observed' reflections). Crystals are monoclinic, P21/a, a 12.815(4), b 17.503(7), c 8.318(3) Ǻ, β 121.38(3)°, Z 2. The complex cation lies with the metal atom on a centre of symmetry, the metal being six-coordinate, so that only one of the tridentate ligands is crystallographically independent. The geometry about the metal atom deviates only trivially from octahedral, <N-Fe-N> within the one ligand being 88.1°. <Fe-N> is 1.982 Ǻ.

Crystal structure of 2,3-Dichloro-5,8-dihydroxynaphtho-1,4-quinone

1978 ◽  
Vol 31 (3) ◽  
pp. 555 ◽  
Author(s):  
GI Feutrill ◽  
CL Raston ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Least Squares ◽  
Benzene Ring ◽  
Title Compound ◽  
X Ray Diffraction ◽  
Hydrogen Atoms ◽  
X Ray ◽  
The One ◽  
Least Squares Techniques

The crystal structure of the title compound has been determined at 295 K by single-crystal X-ray diffraction methods and refined by least- squares techniques to a residual of 0.049 for 1046 'observed' reflections. Crystals are monoclinic, P21/c, a 11.584(6), b 5.449(7), c 15.273(8) Ǻ, β 92.44(4)°, Z4. The pair of quinol hydrogen atoms are both located on the one benzene ring as the title indicates.

Crystal structure of Bis(2,6-diacetylpyridine dihydrazone)cobalt(II) diiodide monohydrate

1978 ◽  
Vol 31 (4) ◽  
pp. 737 ◽  
Author(s):  
BN Figgis ◽  
ES Kucharski ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Least Squares ◽  
High Spin ◽  
Magnetic Moment ◽  
Small Proportion ◽  
Title Compound ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Spin Isomer

The crystal structure of the title compound, [Co(C9H13N5)2] I2,H2O, has been determined by single-crystal X-ray diffraction at 295 K and refined by least squares to a residual of 0.058 for 3255 'observed' reflections. Crystals are triclinic, Pī, a 14.934(5), b 11.315(4), c 8.090(3)Ǻ, α 85.19(3), β 87.76(3), γ 74.10(3)°, Z 2. The distances from the cobalt to the central trimethine nitrogen atoms are 1.893(8) and 1.903(8)Ǻ consistent with the almost low-spin behaviour of the complex; the distal Co-N distances range between 2.045(8) and 2.140(8)Ǻ. One of the iodide anions appears to be disordered over two sites populated in the ratio 0.86:0.14; occupancy of the second site together with the magnetic moment of 2.1 BM may indicate a small proportion of the high-spin isomer.

Crystal structure of Tris(2-methyl-1,10-phenanthroline)iron(II) tetraphenylborate

1983 ◽  
Vol 36 (6) ◽  
pp. 1115 ◽  
Author(s):  
HA Goodwin ◽  
ES Kucharski ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Diffraction Study ◽  
High Spin ◽  
Metal Atom ◽  
Title Compound ◽  
Point Symmetry ◽  
X Ray Diffraction ◽  
X Ray

The crystal structure of the title compound [Fe(mphen)3] (BPh4)2 a high-spin derivative of iron(II), has been determined by a single crystal X-ray diffraction study at 295 K, being refined to a residual of 0.055 for 4079 'observed' reflections. Crystals are monoclinic P 21/c, a 12.326(8), b 15.387(8), c 3679(3) �, β 98.80(6)�, Z 4. The metal atom environment is considerably distorted from ideal D3 point symmetry; Fe-N distances range from 2.143(5) to 2.294(4)�.

Crystal structure of μ-Oxo-bis-fac-[triaqua-1,10-phenanthrolineiron(III)] Tetrakis(nitrate) monohydrate

1984 ◽  
Vol 37 (7) ◽  
pp. 1405 ◽  
Author(s):  
PC Healy ◽  
JM Patrick ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Least Squares ◽  
High Spin ◽  
Iron Atom ◽  
Title Compound ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Spin Iron

The crystal structure of the title compound, [(OH2)3(phen)FeOFe(phen)(OH2)3](NO3)4.(H2O)(phen = 1,10-phenanthroline), has been determined by single-crystal X-ray diffraction methods at 295 K, being refined by least-squares methods to a residual of 0.059 for 3467 independent 'observed'reflections. Crystals are monoclinic, P 21/c, a 18.202(6), b 9.771(4), c 19.459(7) �, β 94.46(3)�, Z = 4. Two of the four anions are disordered. Within the cation, the geometry is typical of high-spin iron(III). O(bridge)-Fe are 1.765(4), 1.784(4) �, with Fe-O-Fe 162.0(3)�. The three water molecules in the coordination sphere of each iron atom are fac; those trans to the O-Fe bond have long Fe-(OH2) distances [2.154(5), 2.125(5) �] compared to those trans to the phenanthroline chelates [2.028(5)-2.037(5) �]. Fe-N range from 2.143(6) to 2.166(6) �.

Crystal structure of ab-Bis(3-methylpyridine)-dc,fe-bis(pentane-2,3,4-trione 3-oximato)iron(II)

1978 ◽  
Vol 31 (11) ◽  
pp. 2431 ◽  
Author(s):  
BN Figgis ◽  
CL Raston ◽  
RP Sharma ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Least Squares ◽  
Title Compound ◽  
X Ray Diffraction ◽  
X Ray ◽  
Chelate Ligands

The crystal structure of the title compound has been determined at 295 K by single-crystal X-ray diffraction and refined by least squares to a residual of 0.062. Crystals are monoclinic, P2/c, a 19.102(8), b 8.117(4), c 16.610(8) Ǻ, β 111.90(3)°, Z. Unlike the tris(α-oxyimino ketonato)iron(II) complexes which are fac, the present derivative is based upon substitution of the two picoline moieties into a mer derivative, trans to the nitrogen atoms of the chelate ligands. <Fe- N(picoline)> is 2.020; <Fe-N, O(chelate)> 1.880, 1.952 Ǻ.

Crystal structure of (Z)-Cembr-4-ene-15,19,20-triol

1977 ◽  
Vol 30 (12) ◽  
pp. 2723 ◽  
Author(s):  
EN Maslen ◽  
CL Raston ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Double Bond ◽  
Single Crystal ◽  
Least Squares ◽  
Structure Determination ◽  
Title Compound ◽  
X Ray Diffraction ◽  
Relative Configuration ◽  
Macrocyclic Ring ◽  
X Ray

The crystal structure of the title compound, CZOH3803 [compound (1) in ref.'], has been determined by single-crystal X-ray diffraction at 295(1) K and refined by least squares to a residual of 0.045 for 954 'observed' reflections. Crystals are monoclinic, P2', a 9.281(2), b 17.798(6), c 6.417(1) A, B 93.81(3)", Z 2. The structure determination establishes the relative configuration of the chiral centres within the 14-membered macrocyclic ring and shows the double bond to have the unusual (Z) configuration.

Crystal Structure of Ethyltriphenylphosphonium Bis(α,α,α',α'-tetracyanoquinodimethanide)

1979 ◽  
Vol 32 (10) ◽  
pp. 2187 ◽  
Author(s):  
RJ Fleming ◽  
MA Shaikh ◽  
BW Skelton ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Least Squares ◽  
Title Compound ◽  
X Ray Diffraction ◽  
X Ray ◽  
Triphenyl Phosphonium

The crystal structure of the title compound, [EtPh3P]+ [(C12H4N4)2]-, has been established by single-crystal X-ray diffraction methods at 295(1) K and refined by least squares to a residual of 0�039 for 3047 'observed' reflections. Crystals are triclinic, Pī, a 8 �882(7), b 13�522(5), c 15�927(6) �, α 75�34(3), β 96�69(5), γ 100.56(3)�, Z 2. The structure closely resembles that of the methyl-triphenyl-phosphonium and -arsonium analogues, containing tetrads of α,α,α',α'- tetracyanoquino- dimethane* molecules, the molecular planes lying parallel to each other and approximately normal to b.

Crystal structure of Aquatetrakis(N-formylpiperidine)dioxouranium(VI) Bisperchlorate

1980 ◽  
Vol 33 (1) ◽  
pp. 69 ◽  
Author(s):  
GJ Honan ◽  
DL Kepert ◽  
SF Lincoln ◽  
JM Patrick ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Water Molecule ◽  
Single Crystal ◽  
Least Squares ◽  
Equatorial Plane ◽  
Title Compound ◽  
Organic Ligands ◽  
X Ray Diffraction ◽  
Uranyl Compounds ◽  
X Ray

The crystal structure of the title compound, [UO2{OCHN(CH2)5}4(H2O)] (ClO4)2, has been determined by single-crystal X-ray diffraction at 295 K and refined by least squares to a residual of 0.051 for 3113 'observed' reflections. Crystals are monoclinic, C2/c, a 16.945(2), b 12.711(2), c 17.304(2)Ǻ, β 107.76(1)°, Z 4. The uranyl moiety [U=O, 1.76(2)Ǻ] is five-coordinated in the equatorial plane by the water molecule [U-O, 2.436(8)Ǻ] and four organic ligands [U-O, 2.379(8), 2.396(13)Ǻ]. The angles O-U-O in the equatorial plane range from 70.3(3) to 73.6(3)°; O=U-0 range between 86.7 and 95.3°. The angle O=U=O is 177.8(3)°. The stereochemistry of seven-coordinate uranyl compounds is examined by using repulsion theory.

Crystal structure of fac-Tris(pentane-2,3,4-trione 3-oximato)cobalt(III)

1978 ◽  
Vol 31 (11) ◽  
pp. 2437 ◽  
Author(s):  
BN Figgis ◽  
CL Raston ◽  
RP Sharma ◽  
AH White
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Least Squares ◽  
Title Compound ◽  
Bidentate Ligands ◽  
X Ray Diffraction ◽  
X Ray ◽  
Independent Molecules

The crystal structure of the title compound has been determined by single-crystal X-ray diffraction at 295 K and refined by least squares to a residual of 0.058 for 2363 'observed' reflections. Crystals are triclinic, Pī, Z 4, a 15.517(8), b 11.772(7), c 11.282(7) Ǻ, α 112.10(4), β 94.80(3), γ 90.60(4)°. <Co-N, O>| distances are 1.883, 1.925 Ǻ respectively, the disposition of the three bidentate ligands within each of the two independent molecules being fac.

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