Syntheses, X-ray Structural Characterizations, and Thermal Stabilities of Two Nonclassical Trinuclear Vanadium(IV) Complexes, (V3(μ3-O)O2)(μ2-O2P(CH2C6H5)2)6(H2O) and (V3(μ3-O)O2) (μ2-O2P(CH2C6H5)2)6(py), and Polymeric Complexes of Stoichiometry (VO(O2PR2)2)∞, R2 = Ph2 and o-(CH2)2(C6H4)

被引:13
|
作者
Maass, John S. [1 ]
Chen, Zhichao [1 ]
Zeller, Matthias [2 ]
Tuna, Floriana [3 ]
Winpenny, Richard E. P. [3 ]
Luck, Rudy L. [1 ]
机构
[1] Michigan Technol Univ, Dept Chem, Houghton, MI 49931 USA
[2] Youngstown State Univ, Dept Chem, Youngstown, OH 44555 USA
[3] Univ Manchester, Sch Chem, Manchester M13 9PL, Lancs, England
关键词
CRYSTAL-STRUCTURE; MAGNETIC-PROPERTIES; OXOVANADIUM(IV) COMPLEXES; DINUCLEAR OXOVANADIUM(IV); COORDINATION POLYMERS; CLUSTERS; LIGANDS; CORE; REACTIVITY; PHOSPHATE;
D O I
10.1021/ic201259u
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The preparation and structural characterization of two trinuclear vanadium complexes, (V-3(mu(3)-O)O-2)(mu(2)-O2P(CH2C6H5)(2))(6)(H2O), 1, and (V-3(mu O3-)O-2)(mu(2)-O2P(CH2C6H5)(2))(6)(py), 2, are reported. In these nonclassical structures, the planar central core consists of the three vanadium atoms arranged in the form of an acute quasi-isosceles triangle with the central oxygen atom multiply bonded to the vanadium atom at the center of the vertex angle and weakly interacting with the two other vanadium atoms on the base sites, each of which contain one external multiply bonded oxygen atom. Reacting VO(acac)(2) in the presence of diphenylphosphinic acid affords (VO(O2Ph2)(2))(infinity), 3, while 2-hydroxyisophosphindoline-2-oxide at room temperature in CH2Cl2 affords ((H2O)VO(O2Po-(CH2)(2)C6H4)(2))(infinity), 4, and at 120 degrees C in EtON yields (VO(O2P(o(CH2)(2)(C6H4))(infinity), 5 on the basis of elemental analyses. The thermal and chemical stability of the complexes were assessed by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) measurements. The bond strengths of the vanadium atoms to the OH2 ligand in 1 and to the NC5H5 ligand in 2 were assessed at 10.7 and 42.0 kJ/mol respectively. Room temperature magnetic susceptibility measurements reveal magnetic moments for trinuclear 1 and 2 at 3.02(1) and 3.05(1) mu(B/mol), and also close to spin only values (1.73 mu(B)) values for 3, 4, and 5 at 1.77(2), 1.758(7), and 1.77(3) mu(B), respectively. Variable-temperature, solid-state magnetic susceptibility measurements were conducted on complex 2 in the temperature range of 2.0-298 K and at an applied field of 0.5 T. Magnetization measurements at 2 and 4 K confirmed a very weak magnetic interaction between the vanadyl centers.
引用
收藏
页码:2766 / 2776
页数:11
相关论文
共 50 条
  • [21] Oxo peroxo glycolato complexes of vanadium(V).: Crystal structure of (NBu4)2 [V2O2(O2)2(C2H2O3)2]•H2O
    Svancárek, P
    Schwendt, P
    Tatiersky, J
    Smatanová, I
    Marek, J
    MONATSHEFTE FUR CHEMIE, 2000, 131 (02): : 145 - 154
  • [22] Oxo peroxo glycolato complexes of vanadium(V). Crystal structure of (NBu4)2[V2O2(O2) 2(C2H2O3)2] H2O
    Švančárek P.
    Schwendt P.
    Tatiersky J.
    Smatanová I.
    Marek J.
    Monatshefte für Chemie / Chemical Monthly, 2000, 131 (2) : 145 - 154
  • [23] THE CRYSTAL-STRUCTURE OF (U[ETA-5-C5](CH3)5][(CH2)(CH2)P(C6H5)2]CL)2(MU-2-O)((MU-3-O)MG[(CH2)P(CH3)(C6H5)2]2)
    CRAMER, RE
    GILJE, JW
    BRUCK, MA
    EDELMANN, F
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1985, 189 (APR-): : 213 - INOR
  • [24] COMPLEXES WITH SUBSTITUTED 2,5-DIHYDROXY-P-BENZOQUINONES - THE INCLUSION-COMPOUNDS [Y(H2O)3]2(C6CL2O4)3.6.6H2O AND [Y(H2O)3]2(C6BR2O4)3.6H2O
    ROBL, C
    MATERIALS RESEARCH BULLETIN, 1987, 22 (11) : 1483 - 1491
  • [25] SOLUBILITY IN THE H3BO3-CH3CH2COOH-H2O, CAB4O7-CH3CH2COOH-H2O, MGB6O10-CH3CH2COOH-H2O SYSTEMS AT 50-DEGREES-C
    KHAZIKHANOVA, BK
    BEREMZHANOV, BA
    SAVICH, RF
    KALACHEVA, VG
    ZHURNAL NEORGANICHESKOI KHIMII, 1981, 26 (11): : 3125 - 3128
  • [26] Syntheses and structures of [Tb(C6NO2H5)3(H2O)2]2n(3nHgCl4)•(4nH2O) and [La(C6NO2H5)2(C6NO2H4)(H2O)2]n(nZnCl4)•(2nH2O)
    Chen, Wentong
    Hu, Long
    Lai, Chunqing
    Zhou, Wenjun
    JOURNAL OF CHEMICAL RESEARCH, 2010, (09) : 533 - 537
  • [27] SYNTHESIS, REACTIVITY AND STRUCTURE OF [MO-3(MU-3-O)2(O2CC6H5)6(H2O)3]2+[W-3(MU-3-O)2(O2CC6H5)6(H2O)3]2+
    DORI, Z
    MARLER, DO
    SCHWOTZER, W
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1984, 187 (APR): : 231 - INOR
  • [28] Synthesis, characterization and crystal structures of three dinuclear diperoxo complexes of Mo(VI): K2{O[MoO(O2)2H2O]2}•2H2O, (C6H8N,NH4){O[MoO(O2)2H2O]2} and (C6H8N,Na){O[MoO(O2)2H2O]2}
    Grzywa, M.
    Nitek, W.
    Lasocha, W.
    JOURNAL OF MOLECULAR STRUCTURE, 2008, 888 (1-3) : 318 - 326
  • [29] Polymer imprinting with iron-oxo-hydroxo clusters: [Fe6O2(OH)2(O2CC(Cl)=CH2)12(H2O)2], [Fe6O2(OH)2(O2C-Ph-(CH)=CH2)12(H2O)2] and [{Fe(O2CC(Cl)=CH2)(OMe)2}10]
    Harben, Spencer M.
    Mosselmans, J. Frederick W.
    Ryan, Aine T.
    Whitwood, Adrian C.
    Walton, Paul H.
    DALTON TRANSACTIONS, 2012, 41 (01) : 208 - 218
  • [30] Synthesis and x-ray diffraction of (CN3H6)2[UO2(C2O4)2(H2O)] • H2O
    Artem'eva, MY
    Mikhailov, YN
    Gorbunova, YE
    Serezhkina, LB
    Serezhkin, VN
    RUSSIAN JOURNAL OF INORGANIC CHEMISTRY, 2005, 50 (08) : 1173 - 1176