Silsesquioxane chemistry II.: Tin(IV) and hafnium(IV) compounds of silsesquioxanes

被引:0
|
作者
Gun'ko, YK
Nagy, L
Brüser, W
Lorenz, V
Fischer, A
Giessmann, S
Edelmann, FT [1 ]
Jacob, K
Vértes, A
机构
[1] Univ Magdeburg, Inst Chem, D-39106 Magdeburg, Germany
[2] Attila Jozsef Univ, Dept Inorgan & Analyt Chem, H-6701 Szeged, Hungary
[3] Univ Halle Wittenberg, Fachbereich Chem, Inst Anorgan Chem, D-06217 Merseburg, Germany
[4] Eotvos Lorand Univ, Dept Nucl Chem, H-1518 Budapest, Hungary
来源
MONATSHEFTE FUR CHEMIE | 1999年 / 130卷 / 01期
关键词
silsesquioxanes; organotin(IV) compounds; Mossbauer spectroscopy; organohafnium(IV) compounds; X-ray crystallography;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Four complexes of silsesquioxanes with di- and triorganotin(IV) cations have been prepared; their composition was determined by standard analytical and spectroscopic methods. The results show that complexes containing an organotin(IV) moiety and the ligand in a 1:1 ratio are formed. FTIR spectra are consistent with the presence of Sn-O vibrations in the compounds. The structure of the complexes is discussed on the basis of Mossbauer and multinuclear ((1)H, (13)C, (119)Sn, and (29)Si) NMR spectroscopic measurements. Comparison of the experimental quadrupole splitting (QS) with that calculated on the basis of the partial quadrupole splitting (PQS) concept revealed that the complexes formed with dialkyltin(IV) cations as well as the trialkyl derivatives have a regular tetrahedral structure. A new organohafnium silsesquioxane derivative ([Cy(7)Si(7)O(12)Hf(C(5)Me(5))], Cy=cyclohexyl, 5), was prepared by treatment of [Cy(7)Si(7)O(9)(OH)(3)] with (C(5)Me(5))HfMe(3) under elimination of methane. The molecular structure of 5 was determined by X-ray crystallography.
引用
收藏
页码:45 / 54
页数:10
相关论文
共 6 条
  • [1] Silsesquioxane chemistry, 4. Silsesquioxane complexes of Titanium(III) and Titanium(IV)
    Edelmann, FT
    Giessmann, S
    Fischer, A
    JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2001, 620 (1-2) : 80 - 89
  • [2] Ethynyl Complexes of Gold(I) Formed by Transmetallation Using Tin(IV) or Silicon(IV) Compounds
    Klauke, Karsten
    Werner, Svenja
    Mohr, Fabian
    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2018, (08) : 1053 - 1056
  • [3] Tin(IV) complexes with diacidic azo(hydrazono) compounds. Crystal structure of bis[4-(2'-hydroxyphenylazo)-3-methyl-1-phenyl-pyrazol-5-onato(2-)]tin(IV)
    Bansse, W
    Jager, N
    Ludwig, E
    Schilde, U
    Uhlemann, E
    Lehmann, A
    Mehner, H
    ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES, 1997, 52 (02): : 237 - 242
  • [4] Homoleptic tin(IV) compounds containing tridentate ONS dithiocarbazate Schiff bases: Synthesis, X-ray crystallography, DFT and cytotoxicity studies
    Yusof, Enis Nadia Md
    Latif, Muhammad A. M.
    Tahir, Mohamed I. M.
    Sakoff, Jennette A.
    Veerakumarasivam, Abhi
    Page, Alister J.
    Tiekink, Edward R. T.
    Ravoof, Thahira B. S. A.
    JOURNAL OF MOLECULAR STRUCTURE, 2020, 1205
  • [5] Chiral sandwich compounds of ruthenium(II) and (IV):: X-ray crystal structure of [Ru{η5-C5H4(neomenthyl)}2I]I3
    Pathak, DD
    Hutton, AT
    Hyde, J
    Walkden, A
    White, C
    JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2000, 606 (02) : 188 - 196
  • [6] Polymorphism in dinuclear Cu(II) compounds-polymorphism caused by different degrees of hydration:: the structures of [Cu(HL)]2Cl24H2O (I), [Cu(HL)]2Cl2•2H2O (II), [Cu(HL)]2)(NO3)2•4H2O (III), [Cu(HL)]2)(NO3)2•2H2O (IV) and [Cu(HL)]2)ClO4)2•2H2O (V) (HL = [(3-aminopropyl)-di-(2-hydroxopropyl)]amine anion).: Counterion control of the crystallization pathway.: Part 11
    Mukhopadhyay, U
    Bernal, I
    INORGANICA CHIMICA ACTA, 2004, 357 (05) : 1360 - 1368