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
相关论文
共 32 条
[11]   ANION CRYPTATES - HIGHLY STABLE AND SELECTIVE MACROTRICYCLIC ANION INCLUSION COMPLEXES [J].
GRAF, E ;
LEHN, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1976, 98 (20) :6403-6405
[12]   Tritopic (cascade) and ditopic complexes of halides with an azacryptand [J].
Hossain, A ;
Morehouse, P ;
Powell, D ;
Bowman-James, K .
INORGANIC CHEMISTRY, 2005, 44 (07) :2143-2149
[13]  
Hossain M. A., 2002, J SUPRAMOL CHEM, V2, P143
[14]   Further insight to selectivity issues in halide binding in a tiny octaazacryptand [J].
Hossain, MA ;
Llinares, JM ;
Miller, CA ;
Seib, L ;
Bowman-James, K .
CHEMICAL COMMUNICATIONS, 2000, (22) :2269-2270
[15]  
Hossain MA, 2002, ANGEW CHEM INT EDIT, V41, P2335, DOI 10.1002/1521-3773(20020703)41:13<2335::AID-ANIE2335>3.0.CO
[16]  
2-3
[17]   Hydrogen bonds between ammonium ions and aromatic rings exist and have key consequences on solid-state and solution phase properties [J].
Ilioudis, CA ;
Bearpark, MJ ;
Steed, JW .
NEW JOURNAL OF CHEMISTRY, 2005, 29 (01) :64-67
[18]   A highly efficient, preorganized macrobicyclic receptor for halides based on CH••• and NH••• anion interactions [J].
Ilioudis, CA ;
Tocher, DA ;
Steed, JW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (39) :12395-12402
[19]   Amide-based ligands for anion coordination [J].
Kang, Sung Ok ;
Begum, Rowshan Ara ;
Bowman-James, Kristin .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (47) :7882-7894
[20]   A hybrid water-chloride structure with discrete undecameric water moieties self-assembled in a heptaprotonated octaamino cryptand [J].
Lakshminarayanan, P. S. ;
Suresh, Eringathodi ;
Ghosh, Pradyut .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (23) :3807-3811