"Breathing" in Adsorbate-Responsive Metal Tetraphosphonate Hybrid Materials

被引:39
作者
Colodrero, Rosario M. P. [2 ]
Cabeza, Aurelio [2 ]
Olivera-Pastor, Pascual [2 ]
Infantes-Molina, Antonia [2 ]
Barouda, Eleni [1 ]
Demadis, Konstantinos D. [1 ]
Aranda, Miguel A. G. [2 ]
机构
[1] Univ Crete, Crystal Engn Growth & Design Lab, Dept Chem, Iraklion 71003, Greece
[2] Univ Malaga, Dept Quim Inorgan, E-29071 Malaga, Spain
关键词
host-guest systems; hybrid materials; hydrogen bonds tetraphosphonates; X-ray diffraction; ORGANIC FRAMEWORKS MIL-100; COORDINATION POLYMERS; PHOSPHONATE MATERIALS; CRYSTAL-STRUCTURE; ADSORPTION; HYDROGEN; INTERCALATION; SORPTION; FUTURE; CARBON;
D O I
10.1002/chem.200900558
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The structures of various layered calcium tetraphosphonates (CaH6DTMP; H8DTMP=hexamethylenediamine tetrakis(methylenephosphonic acid)), have been determined. Starting from CaH6DTMP center dot 2H(2)O, thermal treatment and subsequent exposure to NH3 and/or H2O vapors led to four new compounds that showed high storage capacity of guest species between the layers (up to ten H2O/NH3 molecules) and a maximum volume increase of 55%. The basic building block for these phosphonates consists of an eight-membered ring chelating Ca2+ through two phoshonate groups, and the organic ligand is located within the layers, which are held together by hydrogen bonds. The structural analysis revealed that the uptake/removal of guest species (H2O and NH3) induces significant changes in the framework not only by changing the interlayer distances but also through important conformational changes of the organic ligand. An anisotropic breathing motion could be quantified by the changes of the unit-cell dimensions and ligand arrangements in four crystalline derivatives. Complete characterization revealed the existence of interconversion reactions between the different phases upon gas uptake and release. The observed behavior represents, to the best of our knowledge, the first example of a breathing-like mechanism in metal phosphonates that possess a 2D topology.
引用
收藏
页码:6612 / 6618
页数:7
相关论文
共 59 条
[51]   EXPGUI, a graphical user interface for GSAS [J].
Toby, BH .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2001, 34 :210-213
[52]  
Trens P, 2007, STUD SURF SCI CATAL, V170, P855
[53]   New architectures for zirconium polyphosphonates with a tailor-made open-framework structure [J].
Vivani, R ;
Costantino, F ;
Costantino, U ;
Nocchetti, M .
INORGANIC CHEMISTRY, 2006, 45 (06) :2388-2390
[54]   Exceptional H2 saturation uptake in microporous metal-organic frameworks [J].
Wong-Foy, AG ;
Matzger, AJ ;
Yaghi, OM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (11) :3494-3495
[55]   A tale of two entanglements [J].
Yaghi, Omar M. .
NATURE MATERIALS, 2007, 6 (02) :92-93
[56]   Synthesis, characterization, and amine intercalation behavior of zirconium N-(phosphonomethyl)iminodiacetic acid layered compounds [J].
Zhang, BL ;
Poojary, DM ;
Clearfield, A ;
Peng, GZ .
CHEMISTRY OF MATERIALS, 1996, 8 (06) :1333-1340
[57]   Hysteretic adsorption and desorption of hydrogen by nanoporous metal-organic frameworks [J].
Zhao, XB ;
Xiao, B ;
Fletcher, AJ ;
Thomas, KM ;
Bradshaw, D ;
Rosseinsky, MJ .
SCIENCE, 2004, 306 (5698) :1012-1015
[58]  
Zheng GL, 2004, J CHEM RES-S, P387
[59]  
2008, 1 INT C MET ORG FRAM