Synthetic and Structural Studies in the Lanthanide Toluene-4-sulfonate Hydrates

1992 ◽  
Vol 45 (3) ◽  
pp. 583 ◽  
Author(s):  
DL Faithfull ◽  
JM Harrowfield ◽  
MI Ogden ◽  
BW Skelton ◽  
K Third ◽  
...  

Single-crystal X-ray structure determinations at c. 295 K are reported for representative members of the hydrated toluene-4-sulfonates of the lanthanide elements. The early members of the series, represented by lanthanum, cerium and neodymium, are monoclinic tridecahydrates , space group C2/c, a ≈ 32, b ≈ 7.2, c ≈ 35 �, β ≈ 115 �, Z = 8; the cation is a tricapped trigonal prismatic nonaaqualanthanide (III) species, with three toluene-4-sulfonate counter ions and four lattice water molecules per formula/asymmetric unit. The later members of the series, represented by samarium, lutetium and also yttrium, are, in agreement with contemporary work, monoclinic nonahydrates , space group P21/n, a ≈ 25, b ≈ 7.5, c ≈ 17.8 � , β ≈ 99�, Z = 4; the cation is a square prismatic hexaaquabis (toluene-4-sulfonato)lanthanide(III) species with a single toluene-4-sulfonate counter ion and three lattice water molecules. The solid state dehydration reactions of the tridecahydrates are complicated but there is at least one more endothermic step than is observed for the nonahydrates , with both series of compounds appearing to undergo water loss only below 300�C.


1988 ◽  
Vol 43 (10) ◽  
pp. 1279-1284 ◽  
Author(s):  
Mervat El Essawi ◽  
H Gosmann ◽  
D Fenske ◽  
F Schmock ◽  
K Dehnicke

Triphenylmethylphosphonium nitrite and formate have been prepared by the reaction of [PPh3Me]I with silver nitrite, and lead formate, respectively, in aqueous solutions. [PPh3Me]NO2 (1) forms pale yellow crystals, and [PPh3Me]HCO2·H2O (2) forms white crystals. Both compounds are soluble in water, ethanol, and dichloromethane. In moist air 2 is hydrated to yield [PPh3Me]HCO2·2H2O (3). The compounds were characterized by their IR spectra, 1 and 2 also by X-ray crystal structure determinations.[PPh3Me]NO2 (1): space group P21/n, Z = 4, 2088 independent observed reflexions, R = 0.062. Lattice dimensions (20 °C): a = 914.7(3), b = 1887.5(9), c = 1080.0(4) pm, β = 110.29(3)°. The compound consists of PPh3Me+ ions and NO2- anions with bond lengths of 114.2(6) pm and a bond angle of 124.1(7)°. [PPh3Me]HCO2·H2O (2): space group P21/n, Z = 4, 2973 independent observed reflexions, R = 0.069. Lattice dimensions (-20 °C): a = 931(2), b = 1558(3), c = 1281(2) pm, β = 105.9(1)°. The compound consists of PPh3Me+ ions and formate anions which form centrosymmetric dimeric units [HCO2·H2O]22- through hydrogen bridges of the water molecules. Bond lengths CO 122.4(4) and 120.9(4) pm. bond angle OCO 129.9(4)°.



2000 ◽  
Vol 55 (6) ◽  
pp. 473-478
Author(s):  
J.-U. Rohde ◽  
W. Preetz

By treatment of RhCl3 or IrCl3 with K2C2O4 the bis(oxalato)metallates trans-K3[RhCl2(C2O4)2] and cis-K3[IrCl2(C2O4)2] are formed. From the aqueous solutions single crystals were grown by slow diffusion of ethanol and X-ray structure determinations of trans-K3[RhCl2(C2O4)2] · 4 H2O (monoclinic, space group I2/m, a = 6.218(1), b = 11.837(2), c - 10.357(2) Å, β = 95.55(3)°, Z = 2) and cis-K3[IrCl2(C2O4)2] · H2O (monoclinic, space group /2/a, a = 14.060(3), b = 7.586(2), c = 23.488(5) Å, β = 90.44(3)°, Z = 8) have been performed. The oxalato and chloro ligands of the complex anions are connected via hydrogen bonds and electrostatic interactions to water molecules and potassium ions. The potassium ions are eightfold and in one case ninefold coordinated.



1994 ◽  
Vol 47 (2) ◽  
pp. 339 ◽  
Author(s):  
JM Harrowfield ◽  
WM Lu ◽  
BW Skelton ◽  
AH White

Picrates of dysprosium(III), holmium(III), erbium(III), thulium(III), ytterbium(III), lutetium(III) and yttrium(III) have been found to crystallize as needles from aqueous solution, seemingly best described as 11.5 hydrates. Single-crystal X-ray structure determinations have been performed at c. 295 K on the Dy , Er , Lu and Y species, and show them to be isomorphous , triclinic, Pī , a 20.043(7) → 20.019(5), b 11.533(2) → 11.471(2), c 8.1567(7) → 8.1538(8) Ǻ, α 88.60(1) → 88.40(1), β 87.12(2) → 87.06(1), γ 75.07(2) → 75.05(2)°, V 1819 → 1807 Ǻ3 ( Dy → Lu; the Y and Er values are intermediate). Complex ions [ Ln ( pic )(OH2)7]2+ are observed, with a pair of uncoordinated picrate anions and 4.5 lattice water molecules; this result is in contrast to that of the monoclinic, P 21/c, series found for La → Pr and Nd → Tb, in which the complex cation contains two picrate anions.



2010 ◽  
Vol 66 (6) ◽  
pp. 579-584 ◽  
Author(s):  
Kevin Robertson ◽  
David Bish

X-ray powder diffraction (XRD) data were used to solve the crystal structures of phases in the magnesium perchlorate hydrate system, Mg(ClO4)2·nH2O (n = 4, 2). A heating stage and humidity generator interfaced to an environmental cell enabled in-situ XRD analyses of dehydration reactions under controlled temperatures and partial pressures of H2O (P_{{\rm H}_2{\rm O}}). The crystal structures were determined using an ab initio charge-flipping method and were refined using fundamental-parameter Rietveld methods. Dehydration of magnesium perchlorate hexahydrate to tetrahydrate (348 K) results in a decrease in symmetry (space group = C2), where isolated Mg2+ cations are equatorially coordinated by four H2O molecules with two [ClO4]− tetrahedra at the apices. Further dehydration to the dihydrate (423 K) leads to bridging of the isolated packets to form double corner-sharing chains of octahedra and polyhedra (space group = C2/m).



1975 ◽  
Vol 30 (5-6) ◽  
pp. 462-464 ◽  
Author(s):  
R. Haegele ◽  
W. Verscharen ◽  
D. Babel

The parameters of complete X-ray structure determinations are given for the fluoridesRb2NaFeF6 and Rb2KFeF6 (cubic), Cs2NaCrF6 and Cs2NaFeF6 (hexagonal-rhom-bohedral) and Cs2LiGaF6 (hexagonal). Space group and lattice constants of the monoclinic cyanides Cs2BFe(CN)6 (B = Na, K, Rb) are reported as well.



Crystals ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 222
Author(s):  
Lider ◽  
Sukhikh ◽  
Smolentsev ◽  
Semitut ◽  
Filatov ◽  
...  

Two binuclear coordination compounds of Cu(II) chloride with the bitopic ligand 1,1,2,2-tetrakis(pyrazol-1-yl)ethane (Pz4) of the composition [Cu2(µ2Pz4)(DMSO)2Cl4]·4H2O and [Cu2(µ2Pz4)(DMSO)2Cl4]∙2DMSO were prepared and characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis, single-crystal X-ray diffraction, and powder diffraction analysis. It was shown that in contrast to silver(I) and copper(II) nitrates, copper(II) chloride forms discrete complexes instead of coordination polymers. The supramolecular structure of the complex [Cu2(µ2Pz4)(DMSO)2Cl4]·4H2O with lattice water molecules is formed by OH···Cl and OH···O hydrogen bonds. Density functional theory (DFT) calculations of vibrational frequencies of the ligand and its copper(II) complex allowed for assigning IR bands to specific vibrations.



2020 ◽  
Vol 73 (6) ◽  
pp. 529
Author(s):  
Eric J. Chan ◽  
Simon A. Cotton ◽  
Jack M. Harrowfield ◽  
Brian W. Skelton ◽  
Alexandre N. Sobolev ◽  
...  

Reactions of the lanthanide(iii) picrates (picrate=2,4,6-trinitrophenoxide=pic) with 1,10-phenanthroline (phen) and 2,2′:6′,2′′-terpyridine (terpy) in a 1:2 molar ratio have provided crystals suitable for X-ray structure determinations in instances predominantly involving the lighter lanthanides. In all, the aza-aromatic ligands chelate the lanthanide ion, none being found as ‘free’ ligands within the lattice. The complexes of 1,10-phenanthroline have been characterised in two forms, one unsolvated (Ln=La, Sm, Eu; monoclinic, C2/c, Z 8), one an acetonitrile monosolvate (Ln=Gd; monoclinic, P21/a, Z 4), the latter being the only previously known form (with Ln=La). In both forms, the LnIII is nine-coordinate, in an approximately tricapped trigonal-prismatic environment, with two picrate ligands chelating through phenoxide and 2-nitro group oxygen atoms, the third being bound through phenoxide-O only. The 2,2′:6′,2′′-terpyridine complexes, all acetonitrile monosolvates defined for Ln=La, Gd, Er, and Y (monoclinic, C2/c, Z 4), are ionic, one picrate having been displaced from the primary coordination sphere. For Ln=La, the two bound picrates are again chelating, making the LaIII 10-coordinate in a distorted bicapped square-antiprismatic environment but in the other species they are bound through phenoxide-O only, making the LnIII ions eight-coordinate in a distorted square-antiprismatic environment. Stacked arrays of the ligands can be found in both series of complexes, with intramolecular picrate–picrate and picrate–aza-aromatic stacks being prominent features.



1999 ◽  
Vol 77 (3) ◽  
pp. 313-318 ◽  
Author(s):  
George KH Shimizu ◽  
Gary D Enright ◽  
Gabriela S Rego ◽  
John A Ripmeester

Single crystal X-ray structure determinations of two solvated silver sulfonates have been obtained and these compounds have been shown to adopt infinite one-dimensional motifs. {AgOTs(MeCN)}[Formula: see text] (OTs = p-toluenesulfonate) crystallizes in the monoclinic space group, P21, a = 8.4278(5) Å, b = 5.7413(3) Å, c = 12.1057(7) Å, β = 109.24(1)°. {Ag(NDSA)(MeCN)2(H3O)(H2O)2}[Formula: see text] (NDSA = 1,5-naphthalenedisulfonate) crystallizes in the triclinic space group, P[Formula: see text], a = 8.3407(4) Å, b = 10.4374(5) Å, c = 12.3399(6) Å, α = 101.941(8)°, β = 109.24(1)°, γ = 102.190(8)°. Despite one compound containing a monosulfonate and the other a disulfonate, both complexes form infinite one-dimensional arrays.Key words: silver, sulfonates, coordination polymer.



1999 ◽  
Vol 54 (1) ◽  
pp. 77-86 ◽  
Author(s):  
Jutta Grebe ◽  
Gertraud Geiseler ◽  
Klaus Harms ◽  
Kurt Dehnicke

(Ph4P)X as well as (Me4N)X (X = Cl, Br, I) react with 1,4-diiodotetrafluorobenzene in CH2C12 and CH3CN solutions, respectively, to give the donoracceptor complexes (Ph4PM (C6F4I2)Cl2]·4 CH2Cl2 (1), (Ph4P)2[(C6F4I2)Br2]·2 CH2Cl2 (2), (Me4N)[(C6F4I2)Cl] (3), (Me4N)[(C6F4I2)Br]·CH3CN (4), (Ph4P)2[(C6F4I2)3Br2]·4CH2Cl2 (5), (Ph4P)2[(C6F4I2)3I2] (6) and (Me4N)2[(C6F4I2)3I2] (7). All complexes have been characterized by single X-ray crystallographic structure determinations. 1: Space group P1̄, Z = 1, lattice dimensions at 203 K: a = 1090.2(1), b = 1206.2(1), c = 1242.8(1) pm, α = 91,84(1)°, β = 106.60(1)°, γ = 99.84(1)°.2: Space group P1̄, Z = 1, lattice dimensions at 233 K: a = 1129.7(2), b = 1183.9(1), c = 1293.4(1) pm, α = 65.52(1)°, β = 65.74(1)°, γ = 89.02(1)°.3: Space group P21/n, Z = 4, lattice dimensions at 243 K: a = 714.8(1), b = 2405.7(3), c = 930.8(1) pm, β = 96.38(1)°.4: Space group P21/c, Z = 4, lattice dimensions at 203 K: a = 1400.8(1), b = 1669.9(2), c = 795.9(1) pm, β = 102.81(1)°.5: Space group Pbca, Z = 4, lattice dimensions at 223 K: a = 2106.0(4), b = 1566.8(3), c = 2445.8(4) pm.6 : Space group P1̄, Z = 1, lattice dimensions at 203 K: a = 1150.9(1), b = 1278.9(1), c = 1292.9(2) pm, α = 65.47(1)°, β = 82.07(1)°, γ = 83.62(1)°.7: Space group Pbca, Z = 4, lattice dimensions at 223 K: a = 1210.5(5), b = 1429.0(6), c = 2470.3(12) pm.In all complexes the acceptor molecule C6F4I2 coordinates with the halide donor ions in linear arrangements C-I· · ·X- . In 1 and 2 the halide ions act as terminal donors to form the dianionic species [X· · ·I-C6F4-I· · ·X]2- (X = Cl, Br). Complexes 3 and 4 form polymeric anionic zigzag chains with μ-X- bridges and bond angles I· · ·Cl· · ·I of 77.2° and I· · ·Br· · ·I of 74.3°. Complexes 5 - 7 are characterized by three-dimensional anionic networks via /x3-X- bridging halide ions and μ-bridging 1,4-diiodotetrafluorobenzene molecules.



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