Synthesis and crystal structure of three new bismuth(III) arylsulfonatocarboxylates

被引:5
|
作者
Albat, Martin [1 ]
Inge, Andrew Kentaro [2 ]
Stock, Norbert [1 ]
机构
[1] Christian Albrechts Univ Kiel, Inst Anorgan Chem, Max Eyth Str 2, D-24118 Kiel, Germany
[2] Stockholm Univ, Dept Mat & Environm Chem MMK, SE-10691 Stockholm, Sweden
关键词
bismuth; coordination polymer; sulfonatocarboxylates; COMPLEXES; LIGANDS; CATIONS; PH;
D O I
10.1515/zkri-2016-1980
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
Three new bismuth arylsulfonatocarboxylates [Bi(OH)(SB)] (1), [Bi-4(ST)(2)(HST)O-2(H2O)(2)]center dot H2O (2) and [Bi-4(ST)(2)O-3(H2O)(2)] (3) were synthesized under solvothermal reaction conditions at 180 degrees C using the potassium or sodium salt of 4-sulfobenzoic acid (H2SB) and 2-sulfoterephthalic acid (H3ST), respectively. The compounds were characterized in detail and the crystal structures were determined from single crystal X-ray diffraction data. Phase purity was confirmed by powder X-ray diffraction and elemental analysis. Structural comparisons to the only three other known bismuth sulfonatocarboxylates are presented. Due to the higher reaction temperatures employed for the synthesis of the title compounds a higher degree of condensation of the BiOx polyhedra (X = 7 or 8) to tetrameric units, 1D chains or a 2D layer is observed. Connection through the organic linker molecules leads to the formation of 3D coordination polymers in all three title compounds.
引用
收藏
页码:245 / 253
页数:9
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