Hexabromide salt of a tiny octaazacryptand as a receptor for encapsulation of lower homolog halides: structural evidence on halide selectivity inside the tiny cage

被引:19
作者
Arunachalam, M. [1 ]
Suresh, Eringathodi [2 ]
Ghosh, Pradyut [1 ]
机构
[1] Indian Assoc Cultivat Sci, Dept Organ Chem, Kolkata 700032, W Bengal, India
[2] Cent Salt & Marine Chem Res Inst, CSIR Lab, Analyt Sci Discipline, Bhavnagar 364002, Gujarat, India
关键词
octaazacryptand; halide selectivity; anion encapsulation;
D O I
10.1016/j.tet.2007.08.079
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Tiny azacryptand 1,4,7,10,13,16,21,24-octaazabicyclo[8.8.8]hexacosane (L) upon reaction with 48% hydrobromic acid (containing <0.05% chloride contamination) forms hexabromide salt (1). Single crystal X-ray crystallographic investigation of the hexaprotonated bromide (1) shows no guest encapsulation inside the tiny cage. This bromide salt 1 with an empty proton cage has been utilized as the receptor for encapsulation of chloride (2) and fluoride (3). Crystallographic results of mixed chloride/bromide (2) and fluoride/bromide (3) complexes of L are examined, which show monotopic recognition of chloride in the case of 2 and fluoride in the case of 3 inside the proton cage with five bromide and three water molecules outside the cavity. Single crystals obtained from an experiment on mixed anionic system (chloride and fluoride), 1 shows selective encapsulation of fluoride, which supports the formation of complex 3 and crystals obtained upon treatment of 2 with tetrabutyl ammonium fluoride also yields complex 3. In a separate reaction between L and 49% hydrobromic acid containing higher chloride contamination (<0.2%) forms chloride/bromide salt (2). H-1 NMR studies of 1 with sodium chloride and fluoride support the encapsulation of the respective anions inside the proton cage. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:11371 / 11376
页数:6
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