Tetrahedral Oxyanions in Halogen-Bonded Coordination Networks

被引：33

作者：

Abate, Antonio ^{[1
]}

Marti-Rujas, Javier ^{[2
]}

Metrangolo, Pierangelo ^{[1
,2
]}

Pilati, Tullio ^{[1
]}

Resnati, Giuseppe ^{[1
,2
]}

Terraneo, Giancarlo ^{[1
,2
]}

机构：

[1] Politecn Milan, NFMLab, Dept Chem Mat & Ind Chem Giulio Natta, I-20131 Milan, Italy

[2] PoliMi, CNST, IIT, I-20133 Milan, Italy

来源：

CRYSTAL GROWTH & DESIGN | 2011年 / 11卷 / 09期

关键词：

SCHIFF-BASE COMPLEXES; HALIDE ION SYNTHON; CRYSTAL-STRUCTURES; MOLECULAR-STRUCTURES; ANION COORDINATION; CYANURIC ACID; BR; LIGANDS; IODIDE; SALTS;

D O I：

10.1021/cg200840m

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The deliberate construction of (6,3) networks via halogen bond-driven self-assembly of tetra-n-butylammonium perchlorate, periodate, and perrhenate with 1,4-diiodotetra-fluorobenzene is reported. The mononegative oxyanions sit at network nodes and work as tridentate halogen bond (XB) acceptors, the dliodobenzene derivative spaces the nodes and function as a bidentate XB donor, while the ammonium cations occupy the space encircled by the supramolecular (6,3) frames. Mixed crystals wherein two different oxyanions statistically occupy the network nodes have also been obtained and show geometrical parameters intermediate to the corresponding pure crystals containing only one of the two oxyanions. Mononegative tetrahedral oxyanions are thus demonstrated to behave as general and effective tectons in anion coordination and anion-templated assembly driven by halogen bonding.

引用

页码：4220 / 4226

页数：7

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