Structural variations of nickel complexes in NiS4 and NiS2PN coordination environments: spectral and single-crystal X-ray structural studies on bis(4-methylpiperidinecarbodithioato-S,S′)nickel(II) and (4-methylpiperidinecarbodithioato-S,S′)(thiocyanato-N)(triphenylphosphine)nickel(II)

2009 ◽  
Vol 140 (12) ◽  
pp. 1431-1436 ◽  
Author(s):  
N. Srinivasan ◽  
V. Sathyaselvabala ◽  
K. Kuppulekshmy ◽  
P. Valarmathi ◽  
S. Thirumaran
Keyword(s):  
Single Crystal ◽  
Nickel Complexes ◽  
Structural Studies ◽  
Structural Variations ◽  
X Ray

Cobalt and nickel complexes of open-chain thioether ligands terminated by salicylaldimine functionality*This article has a companion paper in this issue (doi: 10.1139/v11-083).

2011 ◽  
Vol 89 (10) ◽  
pp. 1174-1189 ◽  
Author(s):  
C. Robert Lucas ◽  
John M.D. Byrne ◽  
Julie L. Collins ◽  
Louise N. Dawe ◽  
David O. Miller
Keyword(s):  
Single Crystal ◽  
Electronic Spectra ◽  
Nickel Complexes ◽  
Cobalt Complexes ◽  
Companion Paper ◽  
Cyclic Voltammograms ◽  
Structural Studies ◽  
Open Chain ◽  
X Ray ◽  
Cobalt And Nickel

Syntheses of 1,11-bis(salicylaldimine)-3,6,9-trithiaundecane (H2L1), 1,11-bis(salicylaldimine)-6-oxa-3,9-dithiaundecane (H2L2), and 1,8-bis(salicylaldimine)-3,6-dithiaundecane (H2L3), their nickel complexes [Ni(L1)]·H2O (I), [Ni(HL2)][OAc] (II), [Ni(L3)·HOAc]2[Ni(L3)·2HOAc]·3H2O (III), [Ni(HL1-sal)]Cl2·H2O (IV), [Ni(HL2-sal)]Cl2·CH3OH (V), [Ni(L3-sal)Cl]·H2O (VI), {[Ni(HL1-sal)]Br2}2{[Ni(L1-sal)]Br}·H2O (VII), {[Ni(HL2-sal)]Br2}2{[Ni(L2-sal)]Br}·2CH3OH (VIII), {[Ni(HL3-sal)Br]Br}[Ni(L3-sal)Br]·2CH3OH (IX), [Ni(HL3-sal)Br]Br·CH3OH (X), [Ni(HL3)Br]·2H2O (XI), [Ni(HL1)]2[BF4]2·5H2O (XII), [Ni(HL2)]2[BF4]2·3H2O (XIII), [Ni(HL3)]2[BF4]2·CH3CN (XIV), and [Ni(HL3)]2[BF4]2·3H2O (XV) and their cobalt complexes [Co(L1-sal)][BF4]2 (XVI), [Co(L2)][OAc]·3H2O (XVII), [Co(L3)][OAc]·3H2O (XVIII), [Co(L3)][BF4] (XIX), and [Co(L3-sal)(CH3OH)][BF4]2·CH3OH (XX) are reported. Single crystal X-ray structural studies for III, XIV, XVI, and XIX are described. Cyclic voltammograms of the ligands and of I, II, III, VII, VIII, X, XIV, and XIX are discussed. Electronic spectra of the ligands and complexes are discussed.

Comparative Structural Studies on Three-Coordinate Copper(I) Halide Complexes With Tertiary Phosphines. Crystal Structures of [(PPh2Mes)CuX]2 and [(PPhMes2)CuX]2 (Mes = Mesityl X = Cl, Br, I)

1992 ◽  
Vol 45 (7) ◽  
pp. 1155 ◽  
Author(s):  
GA Bowmaker ◽  
D Camp ◽  
RD Hart ◽  
PC Healy ◽  
BW Skelton ◽  
...  
Keyword(s):  
Single Crystal ◽  
Crystal Structures ◽  
Copper Atom ◽  
Structural Studies ◽  
Coordination Environment ◽  
X Ray ◽  
Tertiary Phosphines ◽  
Structure Determinations ◽  
Halide Complexes ◽  
The Subject

The 1 : 1 complexes of the substituted triphenylphosphine ligands mesityldiphenylphosphine and dimesitylphenylphosphine with copper(1) chloride, bromide and iodide have been the subject of single-crystal X-ray structure determinations at 295 K. All six complexes crystallize as air-stable dimeric molecules, [(PPh2Mes)CuX]2 and [ (PPhMes2)CUX]2 with each copper atom in a distorted trigonal PCuX2. coordination environment. Crystals of [(PPh2Mes)CuCl]2 (1) are monoclinic, P21/n, a 9.961(3), b 18.687(6), c 11.009(7) Ǻ, β 114.63(4)°; R was 0.049 for 2450 'observed' reflections. [(PPh2Mes)CuBrI2 (2) is monoclinic, P21/n, a 9.939(2), b 18.832(6), c 11.238(6) Ǻ, β 115.36(3)°; R was 0.046 for 1803 'observed' reflections. [(PPh2Mes)CuI]2.4/3 C6H6 (3) is rhornbohedral, R3, a 36.877(8), c 9.047(5) A; R was 0.039 for 2537 'observed' reflections. Crystals of [(PPhMes2)CuCl]2.2MeCN (4) are triclinic, Pi, a 15.783(7), b 9.570(4), c 8.914(4) Ǻ, α 72.43(3), β 76.37(3), γ 74.03(3)°; R was 0.045 for 3341 'observed' reflections. [(PPhMes2)CuBr]2.3C6H6 (5) is monoclinic, C2/c, a 9.694(6), b 30.15(2), c 20.66(2) Ǻ, β 98.00(7)°; R was 0.047 for 2117 'observed' reflections. [(PPhMes2)CuI]2.2MeCN (6) is orthorhombic, PP1nb, a 11.694(8), b 14.77(1), c 29.76(3) Ǻ; R was 0.049 for 3447 'observed' reflections. Cu-P bond lengths are: 2.196(2) A (1); 2.198(3) Ǻ (2); 2.222(5) and 2.226(5) Ǻ (3); 2.202(1) Ǻ (4); 2.197(3) A (5); 2.201(4) and 2.264(5) Ǻ (6). The geometries of the LCuX2 and CuX2Cu units are compared with data reported for other monomeric and dimeric compounds for both phosphorus- and nitrogen-based ligands L.

Cation ordering and structural variations with temperature in MgAl2O4spinel: An X-ray single-crystal study

2000 ◽  
Vol 85 (9) ◽  
pp. 1164-1171 ◽  
Author(s):  
Giovanni B. Andreozzi ◽  
Francesco Princivalle ◽  
Henrik Skogby ◽  
Antonio Della Giusta
Keyword(s):  
Single Crystal ◽  
Cation Ordering ◽  
Structural Variations ◽  
X Ray ◽  
Single Crystal Study

Optical, electrical, and X-ray-structural studies on Verneuil-grown SrTiO3 single crystal: Annealing study

2007 ◽  
Vol 401-402 ◽  
pp. 433-436 ◽  
Author(s):  
S. Mochizuki ◽  
F. Fujishiro ◽  
K. Shibata ◽  
A. Ogi ◽  
T. Konya ◽  
...  
Keyword(s):  
Single Crystal ◽  
Structural Studies ◽  
X Ray ◽  
Annealing Study

Iron(II) and Nickel(II) Complexes of 2,6-Di(Thiazol-4-Yl)Pyridine and Related Ligands: Magnetic, Spectral and Structural Studies

1986 ◽  
Vol 39 (2) ◽  
pp. 209 ◽  
Author(s):  
AT Baker ◽  
HA Goodwin
Keyword(s):  
Solid State ◽  
Metal Complexes ◽  
Single Crystal ◽  
Coordination Sphere ◽  
Structural Parameters ◽  
Complex Cation ◽  
Magnetic Behaviour ◽  
Structural Studies ◽  
Thermally Induced ◽  
X Ray

2,6-Di(thiazol-4-yl)pyridine (1a), 2,6-di(2-methylthiazol-4-yl)pyridine (1b) and 2,6-di(2-phenylthiazol-4-yl)pyridine (1c) have been prepared by Hantzsch syntheses from 2,6-di(ω- bromoacetyl )pyridine and the appropriate thioamide. Bis ( ligand ) iron(II) and nickel(II) complexes of (1a) and (1b) have been prepared but no metal complexes of (1c) were isolated. The bis ( ligand ) iron(II) complexes of (1a) are low-spin whereas those of (1b) undergo thermally induced spin-transitions, both in the solid state and solution. The field strengths of the ligands , determined from the spectra of their nickel(II) complexes, correlate well with the observed magnetic behaviour of their iron(II) complexes. The structure of [FeL2][ClO4]2.H2O, L = (1a), was determined by single-crystal X-ray diffractometry . The complex cation has the meridional configuration with the ligand functioning as an approximately planar tridentate. The structural parameters relating to the Fe-N6 coordination sphere are remarkably similar to those found for bis (2,2′:6′, 2′- terpyridine )iron(II) bis ( perchlorate ) monohydrate.

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