Hydrothermal synthesis, structural characterization and magnetic studies of the new pillared microporous ammonium Fe(III) carboxyethylphosphonate:: [NH4][Fe2(OH){O3P(CH2)2CO2}2]

被引:11
作者
Anillo, A
Altomare, A
Moliterni, AGG
Bauer, EM
Bellitto, C
Colapietro, M
Portalone, G
Righini, G
机构
[1] CNR, Ist Struttura Mat, Sez Montelibretti, I-00016 Monterotondo, Italy
[2] Univ Oviedo, Fac Quim, Dept Quim Organ & Inorgan, Inst Quim Organomet E Moles, E-33006 Oviedo, Spain
[3] CNR, Ist Cristallog, I-70125 Bari, Italy
[4] Univ Roma La Sapienza, Dipartimento Chim, I-00185 Rome, Italy
关键词
ammonium iron(III) carboxyethylphosphonate; hydrothermal synthesis; X-ray crystal structure; microporous pillared compound; magnetic properties;
D O I
10.1016/j.jssc.2004.10.047
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The preparation by hydrothermal reaction and the crystal structure of the iron(III) carboxyethylphosphonate of formula [NH4][Fe-2(OH){O3P(CH2)(2)CO2}(2)] is reported. The green-yellow compound crystallizes in the monoclinic system, space group Pc(n.7), with the following unit-cell parameters: a = 7.193(3) A, b = 9.776(3) A, c = 10.17(4) A and beta = 94.3(2)degrees. It shows a typical layered hybrid organic-inorganic structure featuring an alternation of organic and inorganic layers along the a-axis of the unit cell. The bifunctional ligand [O3P(CH2)(2)CO2](3-) is deprotonated and acts as a linker between adjacent inorganic layers, to form pillars along the a-axis. The inorganic layers are made up of dinuclear Fe(III) units, formed by coordination of the metal ions with the oxygen atoms originating from the [O3P-](2-) end of the carboxyethylphosphonate molecules, the oxygen atoms of the [-CO2](-) end group of a ligand belonging to the adjacent layer and the oxygen atom of the bridged OH group. Each Fe(III) ion is six-coordinated in a very distorted octahedral environment. Within the dimer the Fe-Fe separation is found to be 3.5 A, and the angle inside the [Fe(1)-O(11)-Fe(2)] dimers is similar to124degrees. The resulting 3D framework contains micropores delimited by four adjacent dimers in the (bc) planes of the unit cell. These holes develop along the a-direction as tunnel-like pores and [NH4](+) cations are located there. The presence of the p-hydroxo-bridged [Fe(1)-O(11)-Fe(2)] dimers in the lattice is also responsible for the magnetic behavior of the compound at low temperatures. The compound contains Fe3+ ions in the high-spin state and the two Fe(III) ions are antiferromagnetic coupled. The J/k value of -16.3 K is similar to those found for other mu-hydroxo-bridged Fe(III) dimeric systems having the same geometry. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:306 / 313
页数:8
相关论文
共 45 条
[1]  
ALBERTI G, 1999, COMPREHENSIVE SUPRAM, V7, P151
[2]   New techniques for indexing:: N-TREOR in EXPO [J].
Altomare, A ;
Giacovazzo, C ;
Guagliardi, A ;
Moliterni, AGG ;
Rizzi, R ;
Werner, PE .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2000, 33 :1180-1186
[3]   SIR97:: a new tool for crystal structure determination and refinement [J].
Altomare, A ;
Burla, MC ;
Camalli, M ;
Cascarano, GL ;
Giacovazzo, C ;
Guagliardi, A ;
Moliterni, AGG ;
Polidori, G ;
Spagna, R .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1999, 32 :115-119
[4]   Synthesis and characterization of a three-dimensional open-framework lead(II) carboxyethylphosphonate, Pb3(O2CCH2CH2PO3)2 [J].
Ayyappan, S ;
de Delgado, GD ;
Cheetham, AK ;
Férey, G ;
Rao, CNR .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1999, (17) :2905-+
[5]   Iron(III)-phosphonate complexes [J].
Barja, BC ;
Herszage, J ;
Alfonso, MD .
POLYHEDRON, 2001, 20 (15-16) :1821-1830
[6]   Cr[(H3N-(CH2)2-PO3)(Cl)(H2O)]:: X-ray single-crystal structure and magnetism of a polar organic-inorganic hybrid chromium(II) organophosphonate [J].
Bauer, EM ;
Bellitto, C ;
Colapietro, M ;
Portalone, G ;
Righini, G .
INORGANIC CHEMISTRY, 2003, 42 (20) :6345-6351
[7]  
BELLITTO C, 1998, MAGNETISM MOL MAT, V2, P425
[8]   SYNTHESIS OF NEW LAMELLAR IRON(III) PHOSPHONATES [J].
BUJOLI, B ;
PALVADEAU, P ;
ROUXEL, J .
CHEMISTRY OF MATERIALS, 1990, 2 (05) :582-589
[9]   Structural complexity and metal coordination flexibility in two acetophosphonates [J].
Cabeza, A ;
Aranda, MAG ;
Bruque, S .
JOURNAL OF MATERIALS CHEMISTRY, 1998, 8 (11) :2479-2485
[10]   Synthesis, ab initio structure determination, and characterization of manganese(III) phenyl phosphonates [J].
Cabeza, A ;
Aranda, MAG ;
Bruque, S ;
Poojary, DM ;
Clearfield, A .
MATERIALS RESEARCH BULLETIN, 1998, 33 (08) :1265-1274