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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 941-944 
    ISSN: 0044-2313
    Keywords: GdIII trigonal prismatic complexes ; 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 the Lanthanides with Chelate Ligands Synthesis and Crystal Structure of [(py2CH)3Gd]GdBr3 reacts with [(py2CH)Li] to the mononuclear complex [(py2CH)3Gd] 1.The structure of 1 was characterized by X-ray single crystal structure analysis. Space group P21, Z = 2, a = 951.4(10) pm, b = 1369.4(10) pm, c = 1074.5(10) pm, β = 105.69(8)°.The Gd-Ion is surrounded by the six nitrogen atoms of the three chelate ligands and shows a distorted trigonal prismatic coordination. As a difference to the lithium salt of the ligand, the six-membered metalla-cycles in 1 are not planar, but show a boat conformation.
    Notes: GdBr3 reagiert mit [(py2CH)Li] zu dem einkernigen Komplex [(py2CH)3Gd] 1.Der Aufbau von 1 wurde durch eine Kristallstrukturanalyse geklärt: Raumgruppe P21, Z = 2, a = 951,4(10) pm, b = 1369,4(10) pm, c = 1074,5(10) pm, β = 105,69(8)°.Das Gd-Ion ist von den sechs Stickstoff-Atomen der drei Chelatliganden koordiniert und besitzt eine verzerrt trigonalprismatische Umgebung. Die in 1 gebildeten Metalla-Sechsringe sind im Gegensatz zum Lithiumsalz des Liganden nicht planar, sondern zeigen Wannenkonformation.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 945-947 
    ISSN: 0044-2313
    Keywords: Molybdenum(II) ; Mo—Li heterobimetallic complex ; synthesis ; X-ray structure analysis ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Crystal Structure of [Cp2MoHLi(thf)]3 · Toluene[Cp2MoHLi]4 reacts in THF/Toluene to the trimeric complex [Cp2MoHLi(thf)]3 · Toluene 1.The structure of 1 was characterized by X-ray single crystal structure analysis. Space group P63, Z = 2, a = 1459.5(9) pm, c = 1182.3(8) pm. The central unit is represented by a Mo3Li3-hexagon. Each Mo-Atom is surrounded by two Cp-Ligands. One THF-Molecule is coordinated to each Li-atom. The Hydrogen-Ligand could not be located by the single crystal structure analysis.
    Notes: [Cp2MoHLi]4 reagiert in THF/Toluol zu der trimeren Verbindung [Cp2MoHLi(thf)]3 · Toluol 1.Der Aufbau von 1 wurde durch eine Kristallstrukturanalyse geklärt: Raumgruppe P63, Z = 2, a = 1459,5(9) pm, c = 1182,3(8) pm. Die zentrale Einheit in 1 bildet ein Mo3Li3-Sechsring. An jedes Mo-Atom koordinieren zwei Cp-Liganden. Jeweils ein THF-Molekül koordiniert an ein Li-Atom.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 948-952 
    ISSN: 0044-2313
    Keywords: Gadolinium(III) ; Samarium(III) ; pentahedral complexes ; synthesis ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: New Results in the Chemistry of Lanthanoide Complexes. The Crystal Structures of [(C11H21N2)2LnBr] (Ln = Sm, Gd)LnBr3 leads with [(iPr2AIP)Li] (AIP = 2-iPropylamino-4-iPropylimino-2-Pentene) to the mononuclear complex [(iPr2AIP)2LnBr] (Ln = Gd 1, Sm = 2).The structures of 1-2 were characterized by X-ray single crystal structure analysis.1:Space group Cc, Z = 4, a = 1283.3(7) pm, b = 1558.6(8) pm, c = 1330.1(7) pm, β = 90.24(4)°2:Space group Cc, Z = 4, a = 1281.7(2) pm, b = 1562.3(3) pm, c = 1329.8(2) pm, β = 90.09(1)°.The Ln-Ion is coordinated by a Brom-Atom and the four Nitrogen-Atoms of the chelate ligand.
    Notes: LnBr3 reagiert mit [(iPr2AIP)Li] (AIP = 2-iPropylamino-4-iPropylimino-2-Penten) zu dem einkernigen Komplex [(iPr2AIP)2LnBr] (Ln = Gd 1, Sm 2).Der Aufbau von 1-2 konnte durch Kristallstrukturanalyse geklärt werden: 1:Raumgruppe Cc, Z = 4, a = 1283,3(7) pm, b = 1558,6(8) pm, c = 1330,1(7) pm, β = 90,24(4)°.2:Raumgruppe Cc, Z = 4, a = 1281,7(2) pm, b = 1562,3(3) pm, c = 1329,8(2) pm, β = 90,09(1)°. Das Ln-Ion ist durch ein Brom-Atom und die vier Stickstoff-Atome der zwei Chelatliganden fünffach koordiniert.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 1218-1222 
    ISSN: 0044-2313
    Keywords: Phosphoraneiminato Complexes of Vanadium ; Synthesis ; IR spectra ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphoraneiminato Complexes of Vanadium. The Crystal Structure of [V3Cl6(NPMe3)5+]2[V4O4Cl8(NPMe3)22-] · 6 CH3CNVanadiumtetrachloride reacts in CCl4 solution with Me3SiNPMe3 to form the donor acceptor complex [VCl4(Me3SiNPMe3)], which reacts with excess Me3SiNPMe3 in boiling acetonitrile to form the phosphoraneiminato complex [V3Cl6(NPMe3)5]+Cl-. Partial hydrolysis in acetonitrile solution leads to black single crystals of [V3Cl6(NPMe3)5+]2[V4O4Cl8(NPMe3)22-] · 6 CH3CN, which are characterized by a crystal structure determination. Space group P21/c, Z = 2, structure solution with 3 008 observed unique reflections, R = 0.090. Lattice dimensions at -70°C: a = 1 379.0, b = 1 915.8, c = 2 278 pm, β = 102,79°. In the complex cation the three vanadium atoms form a trigonal bipyramid with two μ3-NPMe3 groups; the residual NPMe3- groups and the chlorine atoms are in terminal functions. In the anion [V4O4Cl8(NPMe3)2]2- the vanadium atoms are linked by μ2-O atoms to form a rectangle; in addition the two phosphoraneiminato ligands form μ2-N bridges.
    Notes: Vanadiumtetrachlorid reagiert in CCl4-Lösung mit Me3SiNPMe3 unter Bildung des Donor-Akzeptorkomplexes [VCl4(Me3SiNPMe3)], der sich in siedendem Acetonitril mit weiterem Me3SiNPMe3 zu dem Phosphaniminatokomplex [V3Cl6(NPMe3)5]+Cl- umsetzt. Durch partielle Hydrolyse in Acetonitrillösung entstehen hieraus schwarze Einkristalle [V3Cl6(NPMe3)5+]2[V4O4Cl8(NPMe3)22-] · 6 CH3CN, die wir röntgenographisch charakterisiert haben. Raumgruppe P21/c, Z = 2, Strukturlösung mit 3 008 unabhängigen beobachteten Reflexen, R = 0,090. Gitterkonstanten bei -70°C: a = 1 379,0; b = 1 915,8; c = 2 278 pm, β = 102,79°. In dem komplexen Kation bilden die drei Vanadiumatome mit zwei μ3-NPMe3-Gruppen eine trigonale Bipyramide, die drei übrigen NPMe3-Gruppen und die Chloratome sind terminal gebunden. In dem Anion [V4O4Cl8(NPMe3)2]2- sind die Vanadiumatome über μ2-O-Atome zu einem Rechteck verknüpft; zusätzlich fungieren die beiden Phosphaniminatoliganden als μ2-N-Brücken.
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  • 5
    ISSN: 0044-2313
    Keywords: GdIII ; SmIII ; binuclear complex ; thioureato-ligand ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Thioureato Brigded Binuclear Complexes of the Lanthanides Synthesis and Crystal Structure of [{PhC(NPh)NC(S)NEt2}{Et2NC(S)NH}LnBr(thf)]2 (Ln = Gd, Sm)The reaction of potassium-N-(diethylaminothiocarbonyl)-N′-phenyl-benzamidinat with LnBr3 (Ln = Gd, Sm) leads to the formation of the binuclear complexes [{PhC(NPh)NC(S)NEt2}{Et2NC(S)N}LnBr(thf)]2} (Ln = Gd 1, Sm 2). The two bridging thiureatoligands are probably built during the reaction of potassium with the starting ligand. Coordination by one N-(diethylaminothiocarbonyl)-N′-phenylbenzamidinato-ligand, one Br-ion and one THF-ligand leads to square antiprismatic coordination of the lanthanoids. The structures of both compounds were characterized by X-ray analysis (1: P1 (Nr.2), Z = 1, a = 12,006(4) Å, b = 12,245(4) Å, c = 13,612(3) Å, α = 70,55(3)°, β = 68,21(3)°, γ = 81,31(3)° 2: P1 (Nr.2), Z = 1, a = 11,803(3) Å, b = 12,344(5) Å, c = 12,797(8) Å, α = 103,07(5)°, β = 101,76(3)°, γ = 114,13(3)°)
    Notes: Bei der Reaktion von Kalium-N-(diethylaminothiocarbonyl)-N′-phenyl-benzamidinat mit LnBr3 (Ln = Gd, Sm) bilden sich die zweikernigen Komplexe [{PhC(NPh)NC(S)NEt2}{Et2NC(S)N}LnBr(thf)]2} (Ln = Gd 1, Sm 2). Die Lanthanoidionen werden durch zwei Thioureatoeinheiten verbrückt, die sich vermutlich schon bei der Metallierung des Liganden bilden. Durch zusätzliche Koordination eines N-(Diethylaminothiocarbonyl)-N′-phenyl-benzamidinato-Liganden sowie eines THF-Moleküls und eines Brom-Atoms erhält jedes Lanthanoidion eine quadratisch antiprismatische Koordination.Der Aufbau dieser Verbindungen konnte durch Kristallstrukturuntersuchungen geklärt werden (1: P1 (Nr.2), Z = 1, a = 12,006(4) Å, b = 12,245(4) Å, c = 13,612(3) Å, α = 70,55(3)°, β = 68,21(3)°, γ = 81,31(3)° 2: P1 (Nr.2), Z = 1, a = 11,803(3) Å, b = 12,344(5) Å, c = 12,797(8) Å, α = 103,07(5)°, β = 101,76(3)°, γ = 114,13(3)°)
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  • 6
    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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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 594 (1991), S. 29-35 
    ISSN: 0044-2313
    Keywords: Nickel(12) Cluster ; Synthesis ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of NiCl2 with PhP(SiMe3)2, The Crystal Structure of [Ni12Cl2(PPh)2(P2Ph2)4(PHPh)8][Ni12Cl2(PPh)2(P2Ph2)4(PHPh)8] (1) has been prepared by the reaction of NiCl2 with PhP(SiMe3)2. The structure has been characterized by X-ray crystal structure analysis. 1 contains a Ni12-cluster with m̈4-PPh- and m̈6-P2Ph2- as bridging ligands. The terminal PHPh- and Cl-ligands are bound to Ni-atoms. The Ni12-cluster can be described as an Ni8-cube, in which four edges are bridged by Ni-atoms.
    Notes: NiCl2 und PhP(SiMe3)2 reagieren in THF unter Bildung von [Ni12Cl2(PPh)2(P2Ph2)4(PHPh)8] (1). Die Verbindung bildet schwarze Kristalle, deren Struktur durch eine Kristallstrukturanalyse aufgeklärt werden konnte. Danach liegt ein Ni12-Cluster vor, der m̈4-PPh- und m̈6-P2Ph2-Brückenliganden enthält. Die terminalen PHPh- und Cl-Liganden sind zusätzlich an Ni gebunden. Der Ni12-Cluster kann von einem Ni8-Kubus abgeleitet werden, in dem vier Kanten von Ni-Atomen überbrückt werden.
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  • 8
    ISSN: 0044-2313
    Keywords: Dicyclopentadienyl [bis(trimethylsilyl)phosphanido]titanium, [Cp2TiP(SiMe3)2] ; μ-chloro-μ-bis(trimethylsilyl)arsanido-bis(dicyclopentadienyl)titanium, [(Cp2Ti)2ClAs(SiMe3)2] ; trichloro-bis[tris(trimethylsilyl)phosphane]titanium, [TiCl3{P(SiMe3)3}2] ; syntheses ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of [CpTiCl]2 and TiCl4 with LiE(SiMe3)2 (E = P, As) and P(SiMe3)3. The Crystal Structures of [Cp2TiP(SiMe3)2], [(Cp2Ti)2ClAs(SiMe3)2], and [TiCl3 {P(SiMe3)3}2][Cp2TiCl]2 reacts with LiP(SiMe3)2 to form the mono nuclear complex [Cp2TiP(SiMe3)2] (3). 3 has been characterized by X-ray crystal structure analysis. 3 is paramagnetic and Ti is coordinated by two Cp ligands and a P(SiMe3)2 group. The geometry about the phosphorus atom is nearly trigonal planar. As a result of π-interactions one can find a short Ti—P bond length of about 246.7 pm. In contrast to the formation of 3, the reaction of [Cp2TiCl]2 with LiAs(SiMe3)2 yields the dinuclear Ti complex [(Cp2Ti)2ClAs(SiMe3)2] (4). TiCl4 and P(SiMe3)3 react to from the complex [TiCl3{P(SiMe3)3}2] (2). The Ti atom in 2 is coordinated to three Cl1- and two P(SiMe3)3 ligands.
    Notes: [Cp2TiCl]2 reagiert mit LiP(SiMe3)2 zu dem einkernigen Komplex [Cp2TiP(SiMe3)2] (3). Die Struktur des paramagnetischen 3 konnte mit Hilfe einer Kristallstrukturanalyse aufgeklärt werden. Danach wird das Titanatom von 2 Cp-Liganden und einer P(SiMe3)2-Gruppe koordiniert. Die an P gebundenen Atome liegen dabei in einer Ebene mit dem P-Atom. Als ein Ergebnis der π-Wechselwirkung zwischen Ti und P beobachtet man eine kurze Ti—P-Bindungslänge von 246,7 pm. Dagegen reagiert [Cp2TiCl]2 mit LiAs(SiMe3)2 zu dem zweikernigen Komplex [(Cp2Ti)2ClAs(SiMe3)2] (4). Setzt man TiCl4 mit P(SiMe3)3 um, erhält man weiße Kristalle der Zusammensetzung [TiCl3 {P(SiMe3)3}2] (2). In 2 ist Ti trigonal bipyramidal an die Cl1-- und P(SiMe3)3-Liganden gebunden.
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  • 9
    ISSN: 0044-2313
    Keywords: Zirconium ; vanadium ; hexanuclear Zr—S and V—Se complexes ; preparation ; crystal structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: New Clusters of Zr and V. The Crystal Structures of [Cp6Zr6S9] and [V6Se8O(PMe3)6]The hexanuclear complexes [Cp6Zr6S9] (1) and [V6Se8O(PMe3)6] (2) have been prepared by the reaction of [CpZrCl3] with S(SiMe3)2 and [CpVCl2(PMe3)2] with Se(SiMe3)2, respectively. The structure of 1 consists of discrete [Cp6Zr6S9] molecules with a Zr6 octahedron, coordinated by μ3-Se ligands. In the centre of the Zr6-octahedron is a further μ6-S atom. One can find the same cluster structure in 2, but the V6 octahedron is capped by μ3-Se ligands and the cluster centre is occupied by an oxygen atom.
    Notes: Bei der Reaktion von [CpZrCl3] mit S(SiMe3)2, bzw. von [CpVCl2(PMe3)2] mit Se(SiMe3)2 entstehen die sechskernigen Komplexe [Cp6Zr6S9] (1) bzw. [V6Se8O(PMe3)6] (2). Die Struktur von 1 besteht aus einem Zr6-Oktaeder, dessen Polyederflächen von μ3-S-Liganden besetzt sind, und die Cp-Liganden sind η5 an die Zr-Atome gebunden. Auch in 2 liegt ein Oktaeder vor, das aus 6 V-Atomen gebildet wird und von μ3-Se-Liganden koordiniert wird. 1 und 2 enthalten jeweils im Clusterzentrum ein zusätzliches S-bzw. O-Atom.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 615 (1992), S. 77-80 
    ISSN: 0044-2313
    Keywords: CeIII double decker 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. I. The Crystal Structure of [Li(thf)][(C22H22N4)2Ce] · THFIn THF CeBr3 forms with [(TMTAA)Li2] the paramagnetic doubledecker complex [Li(thf)][(TMTAA)2Ce]. The complex crystallizes with 1 Mol THF per formula unit. The structure was characterized by X-ray single crystal structure analysis (space group C2 (No. 5), z = 6, a = 1741.8(2) pm, b = 1622.1(2) pm, c = 2540.4(3) pm, β = 104.72(1)°). The sandwich-like arrangement of the heterocyclic ligands leads to a quadratic-prismatic coordination of the Ce3+ ion. One macrocyclic ligand is additionally coordinated by a [Li(thf)]+ fragment. The coordination of the Li ion is square pyramidal.
    Notes: CeBr3 reagiert mit [(TMTAA)Li2] in THF zu dem paramagnetischen Doppeldeckerkomplex [Li(thf)][(TMTAA)2Ce], der mit 1 Mol THF pro Formeleinheit kristallisiert. Der Aufbau konnte durch eine Kristallstrukturanalyse aufgeklärt werden (Raumgruppe C2 (Nr. 5), Z = 6, a = 1741,8(2) pm, b = 1622,1(2) pm, c = 2540,4(3) pm, β = 104,72(1)°). Durch die sandwichartige Anordnung der TMTAA-Liganden erhält das Ce3+-Ion eine quadratisch-prismatische Koordination. An einen der makrozyklischen Liganden koordiniert zusätzlich ein [Li(thf)]+-Fragment. Das Li-Ion besitzt tetragonal-pyramidale Umgebung.
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