scholarly journals Reactions in Anhydrous Liquid Ammonia: Syntheses and Crystal Structures of [ M (NH 3 ) 8 ]I 2 ( M = Eu, Yb) with Bicapped Trigonal‐Prismatic Octaammine Lanthanoid(II) Cations

2020 ◽  
Vol 646 (16) ◽  
pp. 1396-1402
Author(s):  
Stefan S. Rudel ◽  
Tim Graubner ◽  
Antti J. Karttunen ◽  
Florian Kraus
2020 ◽  
Vol 76 (8) ◽  
pp. 1213-1221
Author(s):  
Elizabeth C. Manickas ◽  
Matthias Zeller ◽  
Curtis M. Zaleski

The syntheses and crystal structures for the compounds tetra-μ-aqua-tetrakis{2-[azanidylene(oxido)methyl]phenolato}tetrakis(μ2-3-hydroxybenzoato)dysprosium(III)tetramanganese(III)sodium(I) N,N-dimethylacetamide decasolvate, [DyMn4Na(C7H5O3)4(C7H4NO2)4(H2O)4]·10C4H9NO or [DyIIINa(4-OHben)4{12-MCMn(III)N(shi)-4}(H2O)4]·10DMA, 1, and tetra-μ-aqua-tetrakis{2-[azanidylene(oxido)methyl]phenolato}tetrakis(μ2-3-hydroxybenzoato)dysprosium(III)tetramanganese(III)sodium(I) N,N-dimethylformamide tetrasolvate, [DyMn4Na(C7H5O3)4(C7H4NO2)4(H2O)4]·4C3H7NO or [DyIIINa(3-OHben)4{12-MCMn(III)N(shi)-4}(H2O)4]·4DMF, 2, and where MC is metallacrown, shi3− is salicylhydroximate, 3-OHben is 3-hydroxybenzoate, DMA is N,N-dimethylacetamide, 4-OHben is 4-hydroxybenzoate, and DMF is N,N-dimethylformamide, are reported. For both 1 and 2, the macrocyclic metallacrown consists of an [MnIII—N—O] ring repeat unit, and the domed metallacrown captures two ions in the central cavity: a DyIII ion on the convex side of the metallacrown and an Na+ ion the concave side. The MnIII ions are six-coordinate with an elongated tetragonally distorted octahedral geometry. Both the DyIII and Na+ ions are eight-coordinate. The DyIII ions possess a square-antiprismatic geometry, while the Na+ ions have a distorted biaugmented trigonal–prismatic geometry. Four 3-hydroxybenzoate or 4-hydroxybenzoate ligands bridge each MnIII ion to the central DyIII ion. For 1, whole-molecule disorder is observed for the main molecule, excluding only the DyIII and Na+ ions, and the occupancy ratio refined to 0.8018 (14):0.1982 (14). Three DMA molecules were refined as disordered with two in general positions by an approximate 180° rotation and the third disordered twice by general disorder as well as by an exact 180° rotation about a twofold axis that bisects it. The occupancy ratios refined to 0.496 (8):0.504 (8), 0.608 (9):0.392 (9), and 2×0.275 (7):2×0.225 (7), respectively. For 2, segments of the metallacrown are disordered including the DyIII ion, one of the Mn ions, two of the Mn-bound 4-hydroxybenzoate ligands, the Mn-bridging salicylhydroximate ligand, and portions of the remaining three shi3− ligands. The occupancy ratio for the metallacrown disorder refined to 0.849 (9):0.151 (9). Two DMF solvent molecules are also disordered, each over two orientations. The disorder ratios refined to 0.64 (3):0.36 (3) and to 0.51 (2):0.49 (2), respectively. For 2, the crystal under investigation was refined as a non-merohedric twin by a 90° rotation around the real a axis [twin ratio 0.9182 (8):0.0818 (8)].


2015 ◽  
Vol 44 (5) ◽  
pp. 2223-2233 ◽  
Author(s):  
Zhao-Jun Hou ◽  
Zhong-Yi Liu ◽  
Ning Liu ◽  
En-Cui Yang ◽  
Xiao-Jun Zhao

Four magnetic frameworks with hourglass-shaped {Cu5(μ3-OH)2}8+ cluster, linear {Cu3(μ-Cl)2}4+ core, linear {Cu(μ1,1-N3)}+ chain and trigonal-prismatic {Cu8(μ3-tz)6}10+ motifs were reported.


2004 ◽  
Vol 701 (1-3) ◽  
pp. 25-30 ◽  
Author(s):  
Wen-Xin Du ◽  
Jian-Jun Zhang ◽  
Sheng-Min Hu ◽  
Sheng-Qing Xia ◽  
Rui-Biao Fu ◽  
...  

2003 ◽  
Vol 58 (10) ◽  
pp. 939-949 ◽  
Author(s):  
Clemens Reiche ◽  
Uwe Klingebiel ◽  
Mathias Noltemeyer

Dichlorosilanes with bulky substituents R(Me3C)SiCl2 react with liquid ammonia to give geminal silyldiamines [R(Me3C)Si(NH2)2, 1: R = CH2 Me, 2: R = CHMe2]. In the reaction of the monolithium derivatives of these compounds with halosilanes 1-amino-1.3-disilazanes are obtained [(NH2)(Me3C)RSi-NH-SiR1R2R3; 3: R = CMe3, R1 = R2 = R3 = Me; 4: R = R1 = CMe3, R2 = R3 = Me; 5: R = R1 = R2 = CMe3, R3 = H; 6: R = R1 = CMe3, R2 = Me, R3 = F; 7: R = CHMe2, R1 = R2 = R3 = Me]. If monolithiated diamines are treated with trifluorosilanes cyclisation occurs to give (NH-Si(CMe3)2-NH-SiFR)cyclodisilazanes [R = N(SiMe3)(CMe3) (8); R = N(SiMe2CMe3)2 (9)]. 50% of the educts are recovered. The spirocyclic compound 10 is isolated from the reaction of the dilithiated 1-amino-1.3-disilazane 3 with F3SiN(SiMe2CMe3)2. NH-SiF-Functional cyclodisilazanes can be obtained in the reaction of the dilithium derivative of compound 4 with trifluorosilanes [(N(SiMe2CMe3)-Si(CMe3)2-NH-SiFR), R = Ph (11); R = CMe3 (12)]. The lithium derivative of 12 crystallises with TMEDA as adduct 13. In the reaction of the lithiated compound 12 with Me3SiCl, LiCl elimination and substitution of the N-atom is observed (14). The treatment of 13 with PhCHO leads to a 1.3-diaza-5-oxa-2.4-disila-cyclohexane (15 a, b). Starting from lithiated 12 the methoxysubstituted cyclodisiloxane 16 is accessible in the reaction with MeOH. As result of its reactivity towards Me2SiF2 the fluorosilyl-substituted cyclodisilazane 17 is obtained. Crystal structures of 9-11 and 13 have been determined.


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