Redetermination of [Pr(NO3)(3)(H2O)(4)]center dot 2H(2)O

被引:4
|
作者
Decadt, Roel [1 ]
Van Der Voort, Pascal [1 ]
Van Driessche, Isabel [1 ]
Van Deun, Rik [1 ]
Van Hecke, Kristof [1 ]
机构
[1] Univ Ghent, Dept Inorgan & Phys Chem, Krijgslaan 281-S3, B-9000 Ghent, Belgium
关键词
single-crystal X-ray study; T = 100 K; mean sigma(O-N) = 0.003(A)over-circle; R factor = 0.017; wR factor = 0.037; data-to-parameter ratio = 13.2;
D O I
10.1107/S1600536812028024
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
The structure of the title compound, tetraaquatris(nitrato-(KO)-O-2, O0) praseodymium(III) dihydrate, was redetermined. The structure models derived from the previous determinations [ Rumanova et al. (1964). Kristallografiya, 9, 642-654; Fuller & Jacobson (1976). Cryst. Struct. Commun. 5, 349-352] were confirmed, but now with all H atoms unambiguously located, revealing a complex O-H center dot center dot center dot O hydrogen-bonding network, extending throughout the whole structure. In the title compound, the coordination environment of the Pr-III atom can best be described as a distorted bicapped square antiprism defined by three bidentate nitrate anions and four water molecules. Additionally, two lattice water molecules are observed in the crystal packing. The title compound is isotypic with several other lanthanide-containing nitrate analogues.
引用
收藏
页码:I59 / +
页数:9
相关论文
共 50 条
  • [21] Synthesis of complexes of dimethyltin(IV) with mono- and di-deprotonated pyridoxine (PN) in media with various anions. Crystal structures of [SnMe2(PN-H)]NO3 center dot 2H(2)O, [SnMe2(H2O)(PN-H)]-Cl center dot H2O and [SnMe2(H2O)(PN-2H)]center dot 0.5H(2)O
    Casas, JS
    Castellano, EE
    Condori, F
    Couce, MD
    Sanchez, A
    Sordo, J
    Varela, JM
    ZuckermanSchpector, J
    JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1997, (22): : 4421 - 4430
  • [22] Binary systems - Nitrates of metals of the second group of the periodic table and water II-Be(NO3)(2)-H2O, Zn(NO3)(2)-H2O and Cd(NO3)(2)-H2O
    Sieverts, A
    Petzold, W
    ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, 1933, 212 (01): : 49 - 60
  • [23] Valence electronic structure of uranyl nitrate UO2(NO3)(2)center dot 2H(2)O
    Hirata, M
    Monjyushiro, H
    Sekine, R
    Onoe, J
    Nakamatsu, H
    Mukoyama, T
    Adachi, H
    Takeuchi, K
    JOURNAL OF ELECTRON SPECTROSCOPY AND RELATED PHENOMENA, 1997, 83 (01) : 59 - 64
  • [24] Thermal behaviour of [Ca(H2O)4](NO3)2
    Migdal-Mikuli, Anna
    Hetmanczyk, Joanna
    Hetmancyzyk, L.
    JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY, 2007, 89 (02) : 499 - 503
  • [25] Reaction of acetamide with [Pten(H2O)(2)](NO3)(2): Crystal structure of binuclear platinum(II) acetamidate [Pt(2)en(2)(mu-NHCOCH3)(2)](NO3)(2) center dot H2O
    Fedotova, TN
    Minacheva, LK
    Kuznetsova, GN
    Sakharova, VG
    Baranovskii, IB
    ZHURNAL NEORGANICHESKOI KHIMII, 1995, 40 (12): : 1966 - 1972
  • [26] SynthesisandCrystalStructureofaNovel1DCoordinationPolymer:[Pr(BYBA)3(H2O)2]·[Pr(BYBA)3(H2O)]
    孙瑞卿
    曹彦宁
    张汉辉
    陈义平
    杨齐愉
    李超禹
    结构化学, 2007, (11) : 1293 - 1297
  • [27] Thermal behaviour of [Ca(H2O)4](NO3)2
    Anna Migdał-Mikuli
    Joanna Hetmańczyk
    Ł. Hetmańczyk
    Journal of Thermal Analysis and Calorimetry, 2007, 89 : 499 - 503
  • [28] Solubility Modeling of the Binary Systems Fe(NO3)3–H2O, Co(NO3)2–H2O and the Ternary System Fe(NO3)3–Co(NO3)2–H2O with the Extended Universal Quasichemical (UNIQUAC) Model
    Mouad Arrad
    Mohammed Kaddami
    Bahija El Goundali
    Kaj Thomsen
    Journal of Solution Chemistry, 2016, 45 : 534 - 545
  • [29] ASSOCIATION OF N-2 WITH NH4+ AND H3O+(H2O)1, H3O+(H2O)2, H3O+(H2O)3
    GHENO, F
    FITAIRE, M
    JOURNAL OF CHEMICAL PHYSICS, 1987, 87 (02): : 953 - 958
  • [30] Densities of the Ternary Systems Y(NO3)3 + Ce(NO3)3 + H2O, Y(NO3)3 + Nd(NO3)3 + H2O, and Ce(NO3)3 + Nd(NO3)3 + H2O and Their Binary Subsystems at Different Temperatures
    Hu, Yu-Feng
    Jin, Chuan-Wei
    Ling, Shan
    Zhang, Jin-Zhu
    JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2010, 55 (11): : 5031 - 5035