双水汞(II)和三水铊(III)三氟甲烷磺酸盐的结构和键合

A. Molla-Abbassi, L. Eriksson, J. Mink, I. Persson, M. Sandström, M. Skripkin, Ann-Sofi Ullström, P. Lindqvist-Reis
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引用次数: 20

摘要

用单晶x射线衍射、EXAFS和振动光谱研究了双水汞(II)三氟甲烷磺酸盐[Hg(OH2)2(CF3SO3)2]∞和三水铊(III)三氟甲烷磺酸盐[Tl(OH2)3(CF3SO3)3]的结构和键合。双水汞(II)三氟甲烷磺酸盐的晶体结构显示出一种不寻常的连接模式。汞(II)离子与两个水分子的轴向键距为2.11 A,与四个三氟甲烷磺酸离子的四个氧原子形成一个四边形压缩的八面体配位几何,平均键距为2.53 A。两个三氟甲烷磺酸离子在双水汞(II)实体之间形成双桥,产生无限的>Hg(OH2) 2hg (OH2)2<链。平行链由相对较强的氢键结合在一起,O(-H)⋯O的距离在2.688(9)-2.735 (9)a范围内。部分氘化化合物中氢键的O - d拉伸振动频率发生在约2400 cm−1的宽带上,带宽约为170 cm−1。这些层仅通过突出的CF3基团之间的范德华相互作用连接,这与晶体化合物脆弱的片状结构一致。三水铊(III)三氟甲烷磺酸盐结晶为分子络合物,其中每个铊(III)离子结合来自三氟甲烷磺酸盐离子的三个水分子和三个氧原子,Tl-O键距离在2.18-2.24 A范围内。水分子和三氟甲烷磺酸盐离子之间的氢键网络具有O(-H)⋯O距离在2.65(1)-2.80 (1)A范围内将结构结合在一起。记录并分析了拉曼光谱和红外光谱。力常数和振动频率的变化与配位三氟甲磺酸离子中的S-O键、g - o和Tl-O键的键长有关,也与比较中的六价键有关。
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Structure and bonding of bisaquamercury(II) and trisaquathallium(III) trifluoromethanesulfonate
The structure and bonding in bisaquamercury(II) trifluoromethanesulfonate, [Hg(OH2)2(CF3SO3)2]∞, and trisaquathallium(III) trifluoromethanesulfonate, [Tl(OH2)3(CF3SO3)3], have been studied by means of single-crystal X-ray diffraction, EXAFS and vibrational spectroscopy. The crystal structure of bisaquamercury(II) trifluoromethanesulfonate shows an unusual connectivity pattern. The mercury(II) ion strongly binds two water molecules axially with the Hg–O bond distance 2.11 A, and four oxygen atoms from four trifluoromethanesulfonate ions complete a tetragonally compressed octahedral coordination geometry, at the mean Hg–O distance 2.53 A. Two trifluoromethanesulfonate ions form double bridges between the bisaquamercury(II) entities giving rise to infinite >Hg(OH2)2 Hg(OH2)2< chains. The parallel chains are held together in layers by relatively strong hydrogen bonds with O(–H)⋯O distances in the range 2.688(9)–2.735(9) A. The O–D stretching vibrational frequencies of the hydrogen bonds in the partly deuterated compound occur in a broad band at about 2400 cm−1, bandwidth ca. 170 cm−1. The layers are connected only via van der Waals interactions between the protruding CF3 groups, consistent with the fragile sheet-like structure of the crystalline compound. Trisaquathallium(III) trifluoromethanesulfonate crystallises as molecular complexes where each thallium(III) ion binds three water molecules and three oxygen atoms from trifluoromethanesulfonate ions, with Tl–O bond distances in the range 2.18–2.24 A. A hydrogen bond network between the water molecules and trifluoromethanesulfonate ions with O(–H)⋯O distances in the range 2.65(1)–2.80(1) A holds the structure together. Raman and infrared spectra have been recorded and analysed. The changes in force constants and vibrational frequencies have been correlated with bond lengths for the S–O bond in the coordinated trifluoromethanesulfonate ion and for the Hg–O and Tl–O bonds, also including the hexaaquaions in the comparisons.
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