Metal-organic frameworks from two-dimensional copper(II) complexes bridged with N-methylpyrazine-2-carboxamide

被引:4
作者
Yoshida, Mizuki [1 ]
Kanetomo, Takuya [1 ]
Muroyama, Hiroki [1 ]
Ishida, Takayuki [1 ]
Kogane, Tamizo [1 ]
机构
[1] Univ Electrocommun, Dept Engn Sci, Chofu, Tokyo 1828585, Japan
关键词
Pyrazine; Copper(II) ion; Molecule-based magnetic materials; Two-dimensional grid polymer; Metal-organic framework; COORDINATION POLYMERS; MAGNETIC-PROPERTIES; CRYSTAL-STRUCTURE; DESIGN; 4,4'-BIPYRIDINE; CHEMISTRY; CHIRALITY; UNITS;
D O I
10.1016/j.poly.2014.06.056
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two kinds of mpyza-bridged copper(II) complexes, [Cu(mpyza)(2)](BF4)(2)center dot 2H(2)O (1) and [Cu(mpyza)(2)] (PF6)(2)center dot 1.5H(2)O (2) were prepared (mpyza = N-methylpyrazine-2-carboxamide). Their crystal structures have been determined, and despite the different space groups (Pc and P2(1)/c for I and 2, respectively) they exhibit a similar metal-organic framework. Four Cu ions construct rectangular arrangement providing an infinite molecular two-dimensional grid, which have an equatorial-axial-type coordinated pyrazine bridge. Compounds 1 and 2 contain two or one and a half uncoordinated water molecules in a void space. The former liberates the water at 45 degrees C, but the latter does not below 170 degrees C, being consistent with the channel of 1 loosely packed with the counter anion. The magnetic studies revealed that they involved very weak Cu---Cu superexchange antiferromagnetic interactions with J/k(B) = -0.277(5) and -0.166(5) K for 1 and 2, respectively, analyzed on the basis of a two-dimensional model. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:493 / 498
页数:6
相关论文
共 48 条
  • [1] Ligand design for functional metal-organic frameworks
    Almeida Paz, Filipe A.
    Klinowski, Jacek
    Vilela, Sergio M. F.
    Tome, Joao P. C.
    Cavaleiro, Jose A. S.
    Rocha, Joao
    [J]. CHEMICAL SOCIETY REVIEWS, 2012, 41 (03) : 1088 - 1110
  • [2] NEW APPROACH TO THE THEORY OF SUPEREXCHANGE INTERACTIONS
    ANDERSON, PW
    [J]. PHYSICAL REVIEW, 1959, 115 (01): : 2 - 13
  • [3] Supramolecular architectures and magnetic properties of coordination polymers based on pyrazinedicarboxylato ligands showing embedded water clusters
    Beobide, Garikoitz
    Castillo, Oscar
    Luque, Antonio
    Garcia-Couceiro, Urko
    Garcia-Teran, Juan P.
    Roman, Pascual
    [J]. INORGANIC CHEMISTRY, 2006, 45 (14) : 5367 - 5382
  • [4] Crystal engineering of coordination polymers using 4,4′-bipyridine as a bond between transition metal atoms
    Biradha, Kumar
    Sarkar, Madhushree
    Rajput, Lalit
    [J]. CHEMICAL COMMUNICATIONS, 2006, (40) : 4169 - 4179
  • [5] Modular chemistry: Secondary building units as a basis for the design of highly porous and robust metal-organic carboxylate frameworks
    Eddaoudi, M
    Moler, DB
    Li, HL
    Chen, BL
    Reineke, TM
    O'Keeffe, M
    Yaghi, OM
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2001, 34 (04) : 319 - 330
  • [6] Chirality and diastereoselection of Δ/A-configured tetrahedral zinc(II) complexes with enantiopure or racemic Schiff base ligands
    Enamullah, Mohammed
    Vasylyeva, Vera
    Janiak, Christoph
    [J]. INORGANICA CHIMICA ACTA, 2013, 408 : 109 - 119
  • [7] Helical coordination polymers from achiral components in crystals. Homochiral crystallization, homochiral helix winding in the solid state, and chirality control by seeding
    Ezuhara, T
    Endo, K
    Aoyama, Y
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (14) : 3279 - 3283
  • [8] Chiral and achiral crystal structures
    Flack, HD
    [J]. HELVETICA CHIMICA ACTA, 2003, 86 (04) : 905 - 921
  • [9] ON ENANTIOMORPH-POLARITY ESTIMATION
    FLACK, HD
    [J]. ACTA CRYSTALLOGRAPHICA SECTION A, 1983, 39 (NOV): : 876 - 881
  • [10] Control over Flexibility of Entangled Porous Coordination Frameworks by Molecular and Mesoscopic Chemistries
    Furukawa, Shuhei
    Sakata, Yoko
    Kitagawa, Susumu
    [J]. CHEMISTRY LETTERS, 2013, 42 (06) : 570 - 576