Syntheses, crystal structures, and magnetic properties of four novel Cu(I/II) complexes

被引:8
作者
Zhu, Xiaofei [1 ,2 ]
Wang, Ning [3 ]
Li, Bo [4 ]
Zhang, Hong [1 ]
Luo, Yuhui [1 ]
Pang, Yu [1 ]
Tian, Dan [1 ]
机构
[1] NE Normal Univ, Dept Chem, Inst Polyoxometalate Chem, Changchun 130024, Jilin, Peoples R China
[2] Changchun Univ Technol, Sch Chem & Life Sci, Changchun 130012, Jilin, Peoples R China
[3] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
[4] Hebei United Univ, Coll Mat Sci & Engn, Hebei Prov Key Lab Inorgan Nonmetall Mat, Tangshan 063009, Hebei, Peoples R China
关键词
Copper; Coordination complex; Crystal structure; Magnetic properties; METAL-ORGANIC FRAMEWORK; COORDINATION POLYMERS; HYDROTHERMAL SYNTHESIS; LIGAND; PHENANTHROLINE; DIVERSITY; ISOMERISM; ZN(II); ACID;
D O I
10.1016/j.ica.2011.11.020
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Four coordination compounds (CuCuI)-Cu-II(O2N-ipO)(4,4'-bpy) (1), [Cu-6(II)(O2N-ipO)(4)btp(H2O)(8)]center dot 6H(2)O (2), [Cu-12(II)(O2N-ipO)(8)(bth)(4)(H2O)(10)]center dot 2H(2)O (3), and [Cu-18(II)(O2N-ipO)(12)(btp)(3)(H2O)(18)(EtOH)(6)]center dot 13H(2)O (4) (4,4'-bpy = 4,4'-dipyridyl, btp = 1,3-bis(1,2,4-triazol-1-yl)propane, bth = 1,6-bis(1,2,4-triazol-1-yl)hexane and O2N-ipO = deprotonated 5-NO2-2-hydroxyisophthalic acid, Chart 1) were synthesized and crystallographically characterized. The common building unit [Cu-2(O2N-ipO)(2)] (O2N-ipO = deprotonated 5-NO2-2-hydroxyisophthalate, in-situ formed in the reaction of 5-NO2-1,2,3-benzenetricarboxylic acid (O2N-btcH(3)) with CuCl2 center dot 2H(2)O under hydrothermal conditions) features a diamond-shaped dinuclear motif, in which two Cu atoms are bridged by the deprotonated 2-hydroxo groups from different O2N-ipO ligands. Compound 1 exhibits a three-dimensional (3D) wave-like structure composed of [Cu-2(II)(O2N-ipO)(2)](2) and [Cu-2(I)(4,4'-bpy)(2)](2+) subunits, while 2 displaying a 1D alternate double-chain structure based on units of [Cu-2(II)(O2N-ipO)(2)] and [(CuNO4)-N-II]. Compounds 3 and 4 are discrete polynuclear species featuring a dodeca- and a octadeca-nuclear core based on units of [Cu-2(II)(O2N-ipO)(2)] and [(CuNOn)-N-II], respectively. These compounds were further characterized by elemental analyses, FTIR, PXRD and thermogravimetric analyses. In addition, we studied their magnetic properties via direct current magnetic susceptibility measurements. (C) 2011 Elsevier B. V. All rights reserved.
引用
收藏
页码:235 / 243
页数:9
相关论文
共 60 条
[1]   Supramolecular isomerism in coordination compounds: Nanoscale molecular hexagons and chains [J].
Abourahma, H ;
Moulton, B ;
Kravtsov, V ;
Zaworotko, MJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (34) :9990-9991
[2]  
[Anonymous], 1997, SHELXS 97 PROGRAM RE
[3]   Synthesis, structure, and magnetic properties of two new vanadocarboxylates with three-dimensional hybrid frameworks [J].
Barthelet, K ;
Riou, D ;
Nogues, M ;
Férey, G .
INORGANIC CHEMISTRY, 2003, 42 (05) :1739-1743
[4]  
Baum G, 1999, CHEM COMMUN, P195
[5]   BOND-VALENCE PARAMETERS OBTAINED FROM A SYSTEMATIC ANALYSIS OF THE INORGANIC CRYSTAL-STRUCTURE DATABASE [J].
BROWN, ID ;
ALTERMATT, D .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1985, 41 (AUG) :244-247
[6]   EMPIRICAL PARAMETERS FOR CALCULATING CATION-OXYGEN BOND VALENCES [J].
BROWN, ID ;
WU, KK .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1976, 32 (JUL15) :1957-1959
[7]   Solvent hydrolysis and templating effects in the synthesis of metal-organic frameworks [J].
Burrows, AD ;
Cassar, K ;
Friend, RMW ;
Mahon, MF ;
Rigby, SP ;
Warren, JE .
CRYSTENGCOMM, 2005, 7 :548-550
[8]   Co-chelation of a scorpion-shaped carboxylate ligand and phenanthroline lead to a 2-D interpenetratively tubular architecture [J].
Cao, XY ;
Zhang, J ;
Cheng, JK ;
Kang, Y ;
Yao, YG .
CRYSTENGCOMM, 2004, 6 :315-317
[9]   Polycatenation, polythreading and polyknotting in coordination network chemistry [J].
Carlucci, L ;
Ciani, G ;
Proserpio, DM .
COORDINATION CHEMISTRY REVIEWS, 2003, 246 (1-2) :247-289
[10]  
Caulder DL, 1998, ANGEW CHEM INT EDIT, V37, P1840, DOI 10.1002/(SICI)1521-3773(19980803)37:13/14<1840::AID-ANIE1840>3.0.CO