Halide anions driven self-assembly of haloperfluoroarenes: Formation of one-dimensional non-covalent copolymers

被引:58
作者
Abate, Antonio [1 ]
Biella, Serena [1 ]
Cavallo, Gabriella [1 ]
Meyer, Franck [1 ]
Neukirch, Hannes [1 ]
Metrangolo, Pierangelo [1 ]
Pilati, Tullio [2 ]
Resnati, Giuseppe [1 ]
Terraneo, Giancarlo [1 ]
机构
[1] Politecn Milan, Dept Chem Mat & Chem Engn Giulio Natta, NFMLab, I-20131 Milan, Italy
[2] Univ Milan, CNR ISTM, I-20133 Milan, Italy
关键词
Fluorine; Iodine; Halogen bonding; Self-assembly; Crystal engineering; Supramolecular chemistry; SECONDARY BONDING INTERACTIONS; BR-CIRCLE-MINUS; SIGMA-HOLE; INTERMOLECULAR RECOGNITION; SUPRAMOLECULAR CHEMISTRY; MOLECULAR-STRUCTURES; CARBON TETRABROMIDE; CRYSTAL-STRUCTURE; INFINITE CHAINS; HALOGEN BONDS;
D O I
10.1016/j.jfluchem.2009.07.005
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The supramolecular organization in six solid assemblies involving iodo- and bromoperfluoroarene derivatives is described. Single crystal X-ray analyses show that the formation of the supramolecular architectures is controlled by I-center dot center dot center dot Br-Ar-F, I-center dot center dot center dot I-Ar-F, Br-center dot center dot center dot I-Ar-F, and Cl-center dot center dot center dot I-Ar-F halogen bondings thus proving the X-center dot center dot center dot X'-Ar-F supramolecular synthon, where X can be the same as or different from X', is particularly robust. In five of the described architectures halide anions form two halogen bondings and form infinite chains wherein dihaloperfluoroarenes, which function as bidentate electron acceptors, and halide anions, which function as bidentate electron donors, alternate. This behaviour shows halide anions have a fair tendency to work as bidentate halogen bonding acceptors. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1171 / 1177
页数:7
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