Synthesis, crystal structure and 71Ga solid state NMR of a MOF-type gallium trimesate (MIL-96) with μ3-oxo bridged trinuclear units and a hexagonal 18-ring network

被引:71
作者
Volkringer, Christophe
Loiseau, Thierry
Ferey, Gerard
Morais, Claudia M.
Taulelle, Francis
Montouillout, Valerie
Massiot, Dominique
机构
[1] Univ Versailles St Quentin & Yvelines, Porous Solids Grp, Inst Lavoisier, CNRS,UMR 8180, F-78035 Versailles, France
[2] Univ Versailles St Quentin & Yvelines, Tectospin Grp, Inst Lavoisier, CNRS,UMR 8180, F-78035 Versailles, France
[3] CRMHT, CNRS, UPR 4212, F-45071 Orleans, France
关键词
metal-organic framework; hydrothermal synthesis; gallium; trimesic acid; single-crystal XRD; Ga-71 solid state NMR;
D O I
10.1016/j.micromeso.2007.05.018
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A new gallium trimesate Ga12O(OH)(12)({OH}(4), {H2O}(5))[btc](6)center dot approximate to;24H(2)O, called MIL-96 (btc = 1,3,5- benzenetricarboxylate or trimesate species) was hydrothermally synthesized under mild conditions (210 degrees C, 5 h) in the presence of trimethyl 1,3,5-benzene tricarboxylate in water and characterized by single-crystal X-ray diffraction technique. The MIL-96 (Ga) structure exhibits a three-dimensional metalorganic framework containing isolated trinuclear mu(3)-oxo-bridged gallium clusters and infinite chains of GaO4(OH)(2) and GaO2(OH)(4) octahedra generating a hexagonal network based on 18-membered ring. The two types of gallium groups are connected to each other through the trimesate species which induce corrugated chains of gallium octahedra, linked via 1-12-hydroxo bonds with, the specific-cis-cis-trans-sequence. The 3D framework of MIL-96 reveals three kinds of cavities (two of them have estimated pore volumes of approximate to 480 and 860 angstrom(3)), in which are encapsulated free water molecules. The latter species are removed upon beating at 150 degrees C. The MIL-96 (Ga) compound was characterized by Ga-71 solid state NMR at different magnetic fields (14.1 and 17.6 T). Ga-71 spectra of MIL-96 (Ga) show the gallium exhibits relatively weak quadrupolar interactions compared to those observed in other MOF-type gallium carboxylates that have very strong quadrupolar interactions (MIL-61 and MIL-53). (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:111 / 117
页数:7
相关论文
共 49 条
[1]   In(OH)BDC•0.75BDCH2 (BDC = benzenedicarboxylate), a hybrid inorganic-organic vernier structure [J].
Anokhina, EV ;
Vougo-Zanda, M ;
Wang, XQ ;
Jacobson, AJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (43) :15000-15001
[2]   VIII(OH){O2C-C6H4-CO2}•(HO2C-C6H4-CO2H)x(DMF)y(H2O)z (or MIL-68), a new vanadocarboxylate with a large pore hybrid topology:: reticular synthesis with infinite inorganic building blocks? [J].
Barthelet, K ;
Marrot, J ;
Férey, G ;
Riou, D .
CHEMICAL COMMUNICATIONS, 2004, (05) :520-521
[3]   Synthesis, structure determination and magnetic behaviour of the first porous hybrid oxyfluorinated vanado(III)carboxylate:: MIL-71 or VIII2(OH)2F2{O2C-C6H4-CO2}•H2O [J].
Barthelet, K ;
Adil, K ;
Millange, F ;
Serre, C ;
Riou, D ;
Férey, G .
JOURNAL OF MATERIALS CHEMISTRY, 2003, 13 (09) :2208-2212
[4]   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
[5]   [VIII(H2O)]3O(O2CC6H4CO2)3•(Cl, 9H2O) (MIL-59):: a rare example of vanadocarboxylate with a magnetically frustrated three-dimensional hybrid framework [J].
Barthelet, K ;
Riou, D ;
Férey, G .
CHEMICAL COMMUNICATIONS, 2002, (14) :1492-1493
[6]  
Batten SR, 1998, ANGEW CHEM INT EDIT, V37, P1460, DOI 10.1002/(SICI)1521-3773(19980619)37:11<1460::AID-ANIE1460>3.0.CO
[7]  
2-Z
[8]   BOND-VALENCE PARAMETERS FOR SOLIDS [J].
BRESE, NE ;
OKEEFFE, M .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1991, 47 :192-197
[9]  
Cotton F.A., 1988, ADV INORG CHEM
[10]   Crystal engineering of NLO materials based on metal-organic coordination networks [J].
Evans, OR ;
Lin, WB .
ACCOUNTS OF CHEMICAL RESEARCH, 2002, 35 (07) :511-522