| 1. |
- Babizhetskyy, Volodymyr, et al.
(författare)
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Crystal and electronic structures of the new ternary gallide Zr12Pd40−xGa31+y (x = 0–1.5, y = 0–0.5)
- 2023
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Ingår i: Journal of Solid State Chemistry. - 0022-4596 .- 1095-726X. ; 327
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Tidskriftsartikel (refereegranskat)abstract
- Zr12Pd40Ga31 was prepared from the elements by arc melting under argon and subsequent annealing at 870 K for 720 h. Single-crystal X-ray diffraction reveals that Zr12Pd40Ga31 crystallizes in a new hexagonal structure type: Pearson symbol (PS) hP166, space group P6/mmm, a = 18.7670(6) Ǻ, c = 8.6634(6) Ǻ). The crystal structure consists of three types of atomic layers – two flat sheets at z = 0 (layer A) and z = 0.5 (C) and one corrugated at z = 0.25 and z = 0.75 (B), which stack in the sequence … ABCB … along the [001] direction. The structure shows close vicinity to a series of hexagonal structures with PS hP164–hP171. These compounds show peculiar structural variability expressed in the different atomic occupations of the Wyckoff positions along and around the 3-fold and 6-fold axes. Homogeneity range and lattice parameters of new ternary compound Zr12Pd40−xGa31+y (x = 0–1.5, y = 0–0.5) have been refined from EDX and powder XRD data. Electronic structure calculations and bonding analysis have been performed for an idealized model revealing domination of the Pd–Ga and Ga–Ga interactions.
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| 2. |
- Grilli, Davide, et al.
(författare)
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Lan(n+1)+xNin(n+5)+ySi(n+1)(n+2)–z : A Symmetric Mirror Homologous Series in the La–Ni–Si System
- 2023
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Ingår i: Inorganic Chemistry. - : American Chemical Society (ACS). - 0020-1669 .- 1520-510X. ; 62:27, s. 10736-10742
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Tidskriftsartikel (refereegranskat)abstract
- A series of four homologous silicides have been discovered during systematic explorations in the central part of the La–Ni–Si system at 1000 °C. All compounds La12.5Ni28.0Si18.3 (n = 3; a = 28.8686(8), c = 4.0737(2) Å, Z = 3), La22.1Ni39.0Si27.8 (n = 4; a = 20.9340(6), c = 4.1245(2) Å, Z = 1), La32.9Ni49.8Si39.3 (n = 5; a = 24.946(1), c = 4.1471(5) Å, Z = 1), and La44.8Ni66.1Si53.4 (n = 6; a = 28.995(5), c = 4.158(1) Å, Z = 1) crystallize in the hexagonal space group P63/m and can be generalized according to Lan(n+1)+xNin(n+5)+ySi(n+1)(n+2)–z with n = 3–6. Their crystal structures are based on AlB2-type building blocks, fused La-centered Ni6Si6 hexagonal prisms, yielding larger oligomeric equilateral domains with the edge size equal to n. The domains extend along the c axis and show checkered ordering of the cationic and anionic parts, while all their atoms are located on mirror planes. Lan(n+1)+xNin(n+5)+ySi(n+1)(n+2)–z can be considered as a mirror series to the La-rich La(n+1)(n+2)Nin(n–1)+2Sin(n+1), where an exchange of the formal cationic and anionic sites, i.e., La and Si, occurs. The La–Ni–Si system is the first system where two such analogous series have been observed.
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| 3. |
- Hiti, Ethan A., et al.
(författare)
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Exploring the Role of Neutral 4-Amino-1,2,4-triazole in the Formation of Hexanuclear f-Element Hydrolysis Products
- 2024
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Ingår i: Crystal Growth & Design. - 1528-7483 .- 1528-7505. ; 24:2, s. 834-842
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Tidskriftsartikel (refereegranskat)abstract
- Our recent observations of an unexpected Ce(III) hydrolysis product from the reaction of 4-amino-1,2,4-triazole (4-NH2-1,2,4-Triaz) with CeCl3·7H2O, [Ce6(μ3-O)4(μ3-OH)2(μ3-Cl)2(Cl)6(μ2-4-NH2-1,2,4-Triaz)12]·7H2O, the first high-nuclearity lanthanide complex where all Ln atoms are connected pairwise through 12 N-donor ligands or 12 neutral bridging ligands of any type, prompted us to explore the utility of this ligand in trapping additional f-element examples. Reactions of LnCl3·6H2O (Ln = Nd, Eu, Ho) with a large excess of 4-NH2-1,2,4-Triaz (20 equiv) and with the addition of small amounts of water to help solubilize the metal salts led to the isolation of the unique hydrolysis products [Nd6(μ3-OH)8Cl6(μ2-4-NH2-1,2,4-Triaz)12][Cl4]·2H2O, [Eu6(μ6-Cl)0.23(μ3-O0.77)4(μ3-O)2.6(μ3-Cl)0.4Cl6(μ2-4-NH2-1,2,4-Triaz)12], and [Ho6(μ6-Cl)0.21(μ3-O0.79)4(μ3-OH)2Cl6(μ2-4-NH2-1,2,4-Triaz)12][Cl]3.4. We also report a Ce(III) analogue prepared in glassware contaminated with Pb(OAc)2, namely, [Ce6(μ3-OH)8(BrPbBr5)(μ2-4-NH2-1,2,4-Triaz)11.5(OH2)6][Pb0.84Br4.2][Br]3.8·2(4-NH2-1,2,4-Triaz)·3.6H2O. The Nd(III) complex is the structurally most ordered with a clear [Nd6(μ3-OH)8] cluster core, while the Eu(III) and Ho(III) compounds contain partial occupancy of a μ6 position and thus result in an incomplete Ln6O9 cluster core formation. The crystallographic results suggest that the 4-NH2-1,2,4-Triaz ligand brings Ln(III) ions together, followed by the formation of an Ln6O8 or Ln6O9 core with whatever remaining anions or ligands can be incorporated. Given the complexity of the hydrolysis products of nuclear waste, we expect to continue to find a myriad of closely related complex structures of these types for the f-elements.
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| 4. |
- Shtender, Vitalii, et al.
(författare)
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Honeycomb Constructs in the La-Ni Intermetallics : Controlling Dimensionality via p-Element Substitution
- 2023
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Ingår i: Inorganic Chemistry. - : American Chemical Society (ACS). - 0020-1669 .- 1520-510X. ; 62:37, s. 14843-14851
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Tidskriftsartikel (refereegranskat)abstract
- The new ternary compounds La15Ni13Bi5 and La9Ni8Sn5 were obtained by arc melting under argon from appropriate amounts of the elements and subsequent annealing at 800 °C for 2 weeks. Single-crystal X-ray diffraction reveals that they represent two new structure types: La15Ni13Bi5 crystallizes in the hexagonal space group P62m [hP33, a = 14.995(3), c = 4.3421(10) Å, V = 845.5(4) Å3, Z = 1] and La9Ni8Sn5 in P63/m [hP88, a = 23.870(15), c = 4.433(3) Å, V = 2187(3) Å3, Z = 4]. The crystal structures of both compounds are characterized by hexagonal honeycomb-based motifs formed by Ni and Sn that extend along the c axis. The building motif with its three-blade wind turbine shape is reminiscent of the organic molecule triptycene and is unprecedented in extended solids. First-principles calculations have been performed in order to analyze the electronic structure and provide insight into chemical bonding. They reveal significant electron transfer from La to Ni and the respective p-element, which supports the formation of the polyanionic Ni-p-element network. DFT calculations suggest paramagnetic-like behavior for both compounds, which was confirmed by magnetic measurements.
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| 5. |
- Wineinger, Hannah, et al.
(författare)
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Trapping an Unexpected/Unprecedented Hexanuclear Ce(III) Hydrolysis Product with Neutral 4-Amino-1,2,4-triazole
- 2023
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Ingår i: European Journal of Inorganic Chemistry. - : WILEY-V C H VERLAG GMBH. - 1434-1948 .- 1099-1948. ; 26:31
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Tidskriftsartikel (refereegranskat)abstract
- Using Ce(III) as both a representative lanthanide and actinide analog, the ability of mixtures of acidic and basic azoles to allow direct access to homoleptic N-donor f-element complexes in one pot reactions from hydrated salts as starting materials was examined by reacting mixtures of 4-amino-1,2,4-triazole (4-NH2-1,2,4-Triaz), 5-amino-tetrazole (5-NH2-HTetaz), and 1,2,3-triazole (1,2,3-HTriaz) in 1:1 and 1:3 ratios with CeCl3 center dot 7H(2)O, [C(2)mim](3)[CeCl6] ([C(2)mim](+) = 1-ethyl-2-methylimidazolium), and Ce(NO3)(3)center dot 6H(2)O. Although unsuccessful in our goal, structural analysis revealed that neutral 4-NH2-1,2,4-Triaz is structure directing via eta(2)mu(2)kappa(2) bridging, with the formation of the dinuclear complexes [Ce2Cl2(mu(2)-4-NH2-1,2,4-Triaz)(4)(H2O)(8)]Cl-4 center dot 4H(2)O, [Ce-2(mu(2)-4-NH2-1,2,4-Triaz)(4)(4-NH2-1,2,4-Triaz)(2)(Cl)(6)], and [4-NH2-1,2,4-HTriaz][Ce-2(mu(2)-4-NH2-1,2,4-Triaz)(2)(mu(2)-NO3)(NO3)(6)(H2O)(2)]. When the synthetic conditions favored hydrolysis, the hexanuclear Ce(III) complex [Ce-6(mu(3)-O)(4)(mu(3)-OH)(2)(mu(3)-Cl)(2)(Cl)(6)(mu(2)-4-NH2-1,2,4-Triaz)(12)]center dot 7H(2)O was isolated. This unexpected hydrolysis product represents the first example of a high nuclearity lanthanide complex where all Ln atoms are pairwise connected through 12 N-donor ligands or 12 neutral bridging ligands of any type, a rare example of incorporation of non-oxo coordinating anions in the M6X8 core, and the first reported Ce(III) hexanuclear complex of this type.
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