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  • 1
    ISSN: 0044-2313
    Keywords: Rare-Earth Complexes ; Syntheses ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Syntheses and Crystal Structures of the Rare-Earth Complexes [LaI2(THF)5]+I3-, [SmCl3(THF)4], [ErCl2(THF)5]+ [ErCl4(THF)2]-, [ErCl3(DME)2], and [Na(18-Crown-6)(THF)2]+[YbBr4(THF)2]-[LaI2(THF)5]+I3- (1) is obtained as red crystals from lanthanum powder and 1,2-diiodoethane in THF on exposure to light. Space group Pbcn, Z = 4, lattice dimensions at -83°C: a = 1264.9, b = 2218.9, c = 1199.1 pm, R = 0.031. The lanthanum atom of the cation of 1 is coordinated with iodine atoms in the axial positions in a pentagonal-bipyramidal way.[SmCl3(THF)4] (2) originates as colourless crystals on heating SmCl3 with excess THF in the presence of Me3SiNPEt3. Space group P21/c, Z = 8, lattice dimensions at -50°C: a = 3092.7, b = 826.2, c = 1758.3 pm, β = 93.85°, R = 0.054. Just like the known sample that crystallizes within the space group F2dd, 2 forms monomeric molecules in which the samarium atom is coordinated with two chlorine atoms in the axial positions in a distorted pentagonal-bipyramidal way.[ErCl2(THF)5]+[ErCl4(THF)2]- (3). Pale pink single crystals of 3 were prepared according to the described method by reaction of erbium powder with trimethylchlorosilane and methanol in THF. Space group C2/c, Z = 4, lattice dimensions at -50°C: a = 1246.3, b = 1145.7, c = 2726.0 pm, β = 91.293°, R = 0.036. The erbium atom of the cation of 3 has a pentagonal-bipyramidal coordination with the chlorine atoms in the axial positions. Within the anion the THF molecules are in trans-arrangement of the octahedrally coordinated erbium atom.[ErC13(DME)2] (4) originates as pink single crystals from 3 with excess boiling 1,2-dimethoxyethane. Space group P21/c, Z = 4, lattice dimensions at -50°C: a = 1137.2, b = 886.5, c = 1561.1 pm, β = 104.746°, R = 0.032. 4 forms monomeric molecules in which the erbium atom has a pentagonal-bipyramidal surrounding with two chlorine atoms in the axial positions.[Na(18-Krone-6)(THF)2]+ [YbBr4(THF)2]- (5) is formed as by-product by the reaction of YbBr3 with NaN(SiMe3)2 in THF in the presence-of 18-crown-6 forming colourless crystals. Space group P1, Z = 1, lattice dimensions at -70°C: a = 934.6, b = 988.9, c = 1208.0 pm, α = 73.82°, β = 72.98°, γ = 76.89°, R = 0.029. 5 contains isolated [YbBr4(THF)2]-ions, in which the THF molecules are arranged in trans-position.
    Notes: [LaI2(THF)5]+I3- (1) wird aus Lanthanpulver und 1,2-Diiodethan in THF unter Lichteinwirkung als rote Kristalle erhalten. Raumgruppe Pbcn, Z = 4, Gitterkonstanten bei -83°C: a = 1264,9; b = 2218,9; c = 1199,1 pm; R = 0,031. Das Lanthanatom des Kations von 1 ist pentagonal-bipyramidal koordiniert mit den Iodatomen in den Axialpositionen.[SmCl3(THF)4] (2) entsteht beim Erhitzen von SmCl3 mit überschüssigem THF in Gegenwart von Me3SiNPEt3 als farblose Einkristalle. Raumgruppe P21/c, Z = 8, Gitterkonstanten bei -50°C: a = 3092,7; b = 826,2; c = 1758,3 pm; β = 93,85°; R = 0,054. 2 bildet wie das bereits bekannte, in der Raumgruppe F2dd kristallisierende Präparat, monomere Moleküle, in denen das Samariumatom verzerrt pentagonal-bipyramidal koordiniert ist mit zwei Chloratomen in den Axialpositionen.[ErCl2(THF)5]+ [ErCl4(THF)2]- (3). Blaßrosa Einkristalle von 3 erhielten wir nach der literaturbekannten Methode durch Reaktion von Erbiumpulver mit Trimethylchlorsilan und Methanol in THF. Raumgruppe C2/c, Z = 4, Gitterkonstanten bei -50°C: a = 1246,3; b = 1145,7; c = 2726,0 pm; β = 91,293°; R = 0,036. Das Erbiumatom des Kations von 3 hat pentagonal-bipyramidale Koordination mit den Chloratomen in den Axialpositionen, im Anion befinden sich die THF-Moleküle in der trans-Anordnung des oktaedrisch koordinierten Erbiumatoms.[ErCl3(DME)2] (4) entsteht als rosa Einkristalle aus 3 mit überschüssigem, siedendem 1,2-Dimethoxyethan. Raumgruppe P21/c, Z = 4, Gitterkonstanten bei -50°C: a = 1137,2; b = 886,5; c = 1561,1 pm; β = 104,746°; R = 0,032. 4 bildet monomere Moleküle, in denen das Erbiumatom verzerrt pentagonal-bipyramidale Umgebung hat mit zwei Chloratomen in den Axialpositionen.[Na(18-Krone-6)(THF)2]+ [YbBr4(THF)2]- (5) entsteht als Begleitprodukt bei der Umsetzung von YbBr3 mit NaN(SiMe3)2 in THF in Gegenwart von 18-Krone-6 als farblose Kristalle. Raumgruppe P1, Z = 1, Gitterkonstanten bei -70°C: a = 934,6; b = 988,9; c = 1208,0 pm; α = 73,82°; β = 72,98°; γ = 76,89°; R = 0,029. 5 enthält isolierte [YbBr4(THF)2]--Ionen, in denen die THF-Moleküle in trans-Stellung angeordnet sind.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 615 (1992), S. 81-85 
    ISSN: 0044-2313
    Keywords: SmIII polynuclear complex ; CoII complex ; synthesis ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Reaction of Macrocycles with Lanthanoids. II. The Crystal Structures of [K(thf)3]2[(C22H28N4)2Sm2] · 4 THF and [(C22H22N4)Co] · DMEIn a complicated redox reaction [(TMTAA)K2] and [SmI2(thf)2] form the polynuclear metal complex [K(thf)3]2[(TMTAT)2Sm2]. This complex crystallizes with four molecules THF per formula unit and its structure was determined by single crystal X-ray investigation (spacegroup P21/c (No. 14), z = 4, a = 998.0(2) pm, = b = 2618.3(6) pm, c = 1619.4(3) pm, β = 96.52(2)°). In the dimeric unit [(TMTAT)2Sm2]2- the Sm3+ ions are bonded to the four N atoms of the macrocyclic ligand and one C6H4 ring of the second ligand is attached η6 like to one metal ion. Additionally two [K(thf)3]+ fragments are bonded to this central unit, and therefor coordination number seven results for the K+ ion. [TMTAA]2- is not reduced by [Cp2Co] in a similar reaction. The monomeric paramagnetic complex [(TMTAA)Co] (μeff = 2,76 μB) is formed instead. The structure reveils a square planar coordination of the Co atom by the four N atoms of the TMTAA ligand (spacegroup C2/c (No. 15), z = 4, a = 1945.1(4) pm, b = 1165.6(2) pm, c = 1144.7(2) pm, β = 116.38(1)°).
    Notes: [(TMTAA)K2] und [SmI2(thf)2] reagieren in einer unübersichtlichen Redoxreaktion zu dem mehrkernigen Metallkomplex [K(thf)3]2[(TMTAT)2Sm2]. Der Aufbau dieser mit vier Molekülen THF pro Formeleinheit kristallisierenden Verbindung konnte durch eine Röntgenstrukturanalyse aufgeklärt werden (Raumgruppe P21/c (Nr. 14), Z = 4, a = 998,0(2) pm, b = 2618,3(6) pm, c = 1619,4(3) pm, β = 96,52(2)°). In der dimeren Einheit [(TMTAT)2Sm2]2- sind die Sm3+-Ionen außer an die vier N-Atome eines makrozyklischen Liganden auch η6-artig an einen C6H4-Ring des zweiten Liganden gebunden. Zusätzlich koordinieren an die zentrale Einheit zwei [K(thf)3]+-Fragmente. Dies führt zu einer Koordinationszahl von 7 für das K+-Ion. [TMTAA]2- wird in einer analogen Reaktion mit [Cp2Co] nicht reduziert. Statt dessen bildet sich der monomere paramagnetische Komplex [(TMTAA)Co] (μeff = 2,76 μB). Nach der Kristallstrukturanalyse ist das Co-Atom quadratisch planar von den vier N-Atomen des TMTAA-Liganden koordiniert (Raumgruppe C2/c (Nr. 15), Z = 4, a = 1945,1(4) pm, b = 1165,6(2) pm, c = 1144,7(2) pm, β = 116,38(1)°).
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  • 3
    ISSN: 0044-2313
    Keywords: Chromium ; Palladium ; Copper Phosphaneimine Complexes ; Syntheses ; IR Spectra ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Silylated Phosphaneimine Complexes of Chromium(II), Palladium(II), and Copper(II). The Crystal Structures of [CrCl2(Me3SiNPMe3)2], [PdCl2(Me3SiNPEt3)2], and [CuCl2(Me3SiNPMe3)]2The title compounds have been prepared by the reaction of the silylated phosphaneimines Me3SiNPR3 (R = CH3, C2H5) with CrCl2(THF)2, PdCl2 and CuCl2, respectively, in dichloromethane suspensions. All donor-acceptor complexes were characterized by IR spectroscopy and by crystal structure determinations.[CrCl2(Me3SiNPMe3)2]: Space group Pccn, Z = 4, structure determination with 2104 observed unique reflections, R = 0.045. Lattice dimensions at -70°C: a = 1326.3, b = 1562.5, c = 1171.5 pm. Within the monomeric molecular structure the chromium atom is planarly coordinated within the trans-configuration of the Cl atoms and the N atoms with distances of Cr—Cl = 235.94 pm and Cr—N = 211.7 pm.[PdCl2(Me3SiNPEt3)2]: Space group P21/n, Z = 2, structure determination with 2412 observed unique reflections, R = 0.031. Lattice dimensions at 20°C: a = 917.3, b = 1390.2, c = 1161.7 pm, β = 95.80°. Within the monomeric molecular structure the palladium atom is planarly coordinated within the trans-configuration of the Cl atoms and the N atoms with distances of Pd—Cl = 222.9 pm and Pd—N = 209.5 pm.[CuCl2(Me3SiNPMe3)2]: Space group Pbca, Z = 4, structure determination with 1861 observed unique reflections, R = 0.067. Lattice dimensions at -70°C: a = 1440.2, b = 1205.1, c = 1536.5 pm. The compound forms centrosymmetric dimeric molecules, in which the Cu atoms are linked via almost symmetrical chloro-bridges with Cu—Cl distances of 231.4 pm. The distance Cu—N is 196.7 pm.
    Notes: Die Titelverbindungen entstehen bei der Einwirkung der silylierten Phosphanimine Me3SiNPR3 (R = CH3, C2H5) auf CrCl2(THF)2, PdCl2 und CuCl2 in Dichlormethan-Suspension. Die drei Donor-Acceptor-Komplexe werden durch ihre IR-Spektren und durch Kristallstrukturanalysen charakterisiert.[CrCl2(Me3SiNPMe3)2]: Raumgruppe Pccn, Z = 4, Strukturlösung mit 2104 unabhängigen beobachteten Reflexen, R = 0,045. Gitterkonstanten bei -70°C: a = 1326,3; b = 1562,5; c = 1171,5 pm. In der monomeren Molekülstruktur ist das Chromatom planar in der trans-Konfiguration von den Cl-Atomen und den N-Atomen der Phosphanimin-Liganden koordiniert mit Abständen Cr—Cl = 235,94 pm und Cr—N = 211,7 pm.[PdCl2(Me3SiNPEt3)2]: Raumgruppe P21/n, Z = 2, Strukturlösung mit 2412 unabhängigen beobachteten Reflexen, R = 0,031. Gitterkonstanten bei 20°C: a = 917,3; b = 1390,2; c = 1161,7 pm, β = 95,80°. In der monomeren Molekülstruktur ist das Palladiumatom planar in der trans-Konfiguration von den Cl-Atomen und den N-Atomen der Phosphaniminliganden koordiniert mit Abständen Pd—Cl = 222,9 pm und Pd—N = 209,5 pm.[CuCl2(Me3SiNPMe3)]2: Raumgruppe Pbca, Z = 4, Strukturlösung mit 1861 unabhängigen beobachteten Reflexen, R = 0,067. Gitterkonstanten bei -70°C: a = 1440,2; b = 1205,1; c = 1536,5 pm. Die Verbindung bildet zentrosymmetrische dimere Moleküle, in denen die Cu-Atome über nahezu symmetrische Chlorobrücken mit Cu—Cl-Abständen von 231,4 pm verknüpft sind. Der Abstand Cu—N beträgt 196,7 pm.
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  • 4
    ISSN: 0044-2313
    Keywords: Phosphoraneiminato Complexes ; Boron Compounds ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphaneimine and Phosphoraneiminato Complexes of Boron. Synthesis and Crystal Structures of [BF3(Me3SiNPEt3)], [BCl2(NPPh3)]2, [BCl2(NPEt3)]2, [B2Cl3(NPEt3)2]+BCl4-, and [B2Cl2(NPiPr3)3]+BCl4-The title compounds have been prepared from the corresponding silylated phosphaneimines and boron trifluoride etherate and boron trichloride, respectively. The compounds form white moisture sensitive crystals, which were characterized by 11B-nmr-spectroscopy, IR-spectroscopy and by crystal structure determinations.[BF3(Me3SiNPEt3)]: Space group P21/c, Z = 4, R = 0.032 for reflections with I 〉 2σ(I). Lattice dimensions at -70°C: a = 1361.0, b = 819.56, c = 1422.5 pm, β = 109.86°. The donor acceptor complex forms monomeric molecules with a B—N bond length of 157.8 pm.[BCl2(NPPh3)]2 · 2 CH2Cl2: Space group P21/c, Z = 2, R = 0.049 for reflections with I 〉 2σ(I). Lattice dimensions at -50°C: a = 1184.6, b = 2086.4, c = 843.0 pm, β = 96.86°. The compound forms centrosymmetric dimeric molecules in which the boron atoms are linked to B2N2 four-membered rings with B—N distances of 152.7 pm via μ2-N bridges of the NPPh3 groups.[BCl2(NPEt3)]2: Space group Pbca, Z = 4, R = 0.029 for reflections with I 〉 2σ(I). Lattice dimensions at -90°C: a = 1269.5, b = 1138.7, c = 1470.3 pm. The compound has a molecular structure corresponding to the phenyl compound with B—N ring distances of 151.0 pm.[B2Cl3(NPEt3)2]+BCl4-: Space group Pbca, Z = 8, R = 0.034 for reflections with I 〉 2σ(I). Lattice dimensions at -70°C: a = 1309.3, b = 1619.8, c = 2410.7 pm. Within the cations the boron atoms are linked to planar, asymmetrical B2N2 four-membered rings with B—N distances of 155.1 and 143.1 pm via the μ2-N atoms of the NPEt3 groups.[B2Cl2(NPiPr3)3]+BCl4- · CH2Cl2: Space group Pna2, Z = 4, R = 0.033 for reflections with I 〉 2σ(I). Lattice dimensions at -70°C: a = 1976.5, b = 860.2, c = 2612.7 pm. Within the cations the boron atoms are linked to planar, asymmetrical B2N2 four-membered rings with B—N distances of 153.7 and 150.5 pm via the μ2-N atoms of two of the NPiPr3 groups. The third NPiPr3 group is terminally connected to the sp2-hybridized boron atom with a B—N distance of 133.5 pm and with a B—N—P bond angle of 165.3°.
    Notes: Die Titelverbindungen werden aus den entsprechenden silylierten Phosphaniminen Me3SiNPR3 und Bortrifluorid-Etherat bzw. Bortrichlorid hergestellt. Die Verbindungen bilden weiße, feuchtigkeitsempfindliche Kristalle, die wir durch 11B-NMR- und IR-Spektren sowie durch Kristallstrukturanalysen charakterisiert haben.[BF3(Me3SiNPEt3)]: Raumgruppe P21/c, Z = 4, R = 0,032 für Reflexe mit I 〉 2σ(I). Gitterkonstanten bei -70°C: a = 1361,0; b = 819,56; c = 1422,5 pm, β = 109,86°. Der Donor-Akzeptor-Komplex bildet monomere Moleküle mit einer B—N-Bindungslänge von 157,8 pm.[BCl2(NPPh3)]2 · 2 CH2Cl2: Raumgruppe P21/c, Z = 2, R = 0,049 für Reflexe mit I 〉 2σ(I). Gitterkonstanten bei -50°C: a = 1184,6; b = 2086,4; c = 843,0 pm; β = 96,86°. Die Verbindung bildet zentrosymmetrische dimere Moleküle, in denen die Boratome über μ2-N-Brücken der NPPh3-Gruppen zu B2N2-Vierringen mit B—N-Abständen von 152,7 pm verknüpft sind.[BCl2(NPEt3)]2: Raumgruppe Pbca, Z = 4, R = 0,029 für Reflexe mit I 〉 2σ(I). Gitterkonstanten bei -90°C: a = 1269,5; b = 1138,7; c = 1470,3 pm. Die Verbindung hat einen zu der Phenylverbindung entsprechenden Aufbau mit B—N-Ringabständen von 151,0 pm.[B2Cl3(NPEt3)2]+BCl4-: Raumgruppe Pbca, Z = 8, R = 0,034 für Reflexe mit I 〉 2σ(I). Gitterkonstanten bei -70°C: a = 1309,3; b = 1619,8; c = 2410,7 pm. In den Kationen sind die Boratome über die μ2-N-Atome der NPEt3-Gruppen zu planaren, asymmetrischen B2N2-Vierringen mit B—N-Abständen von 155,1 und 143,1 pm verknüpft.[B2Cl2(NPiPr3)3]+BCl4- · CH2Cl2: Raumgruppe Pna21, Z = 4, R = 0,033 für Reflexe mit I 〉 2σ(I). Gitterkonstanten bei -70°C: a = 1976,5; b = 860,2; c = 2612,7 pm. In den Kationen sind die Boratome durch die μ2-N-Atome zweier NPiPr3-Gruppen zu planaren, asymmetrischen B2N2-Vierringen mit B—N-Abständen von 153,7 und 150,5 pm verknüpft. Die dritte NPiPr3-Gruppe ist mit dem sp2-hybridisierten Boratom terminal mit einem B—N-Abstand von 133,5 pm verbunden bei einem B—N—P-Bindungswinkel von 165,3°.
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