Anion and Cation Effects on Anion-Templated Assembly of Tetrahydroxytriptycene

被引:15
作者
White, Nicholas G. [1 ]
MacLachlan, Mark J. [1 ]
机构
[1] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Anion and Cation Effects on Anion-Templated Assembly of; Tetrahydroxytriptycene; METAL-ORGANIC FRAMEWORKS; MOLECULAR RECOGNITION; COMPUTER-PROGRAM; BUILDING-BLOCKS; BINDING; RECEPTOR; COMPLEXES; SOLVENT; CAGE; NMR;
D O I
10.1021/acs.cgd.5b01342
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A tetrahydroxytriptycene ligand 1 assembles through O-H center dot center dot center dot anion hydrogen bonds into a range of different structures. With tetrabutylammonium bromide, 1 forms a stable nanotube structure that is supported by O-H center dot center dot center dot anion hydrogen bonds, but its space is occupied by the large cation. In an effort to produce the nanotubes with different cations and anions, 1 was crystallized with different salts. The reaction of 1 with tetraethylammonium bromide gives a 2D net structure, while 1 and tetrapropylammonium bromide give a discrete 1:2 complex. Attempting to co-crystallize 1 and tetramethylammonium bromide gave crystals of an oxidized quinone form of the ligand. When 1 was crystallized with tetrabutylammonium terephthalate, two different one-dimensional anion coordination polymers were obtained, depending on the crystallization solvent: acetonitrile gave a zigzag polymer, while methanol gave a linear structure. In both cases, the tetrabutylammonium cations fill the gaps between the ID polymers, giving a layered 2D morphology. The wide range of architectures prepared from a relatively simple ligand illustrates the potential utility of O-H center dot center dot center dot anion interactions for constructing solid-state materials.
引用
收藏
页码:5629 / 5636
页数:8
相关论文
共 96 条
[1]   Reactivity of ions and ion pairs in the nucleophilic substitution reaction on methyl p-nitrobenzenesulfonate [J].
Alunni, S ;
Pero, A ;
Reichenbach, G .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1998, (08) :1747-1750
[2]   A cartography of the van der Waals territories [J].
Alvarez, Santiago .
DALTON TRANSACTIONS, 2013, 42 (24) :8617-8636
[3]   Anion recognition by hydrogen bonding: urea-based receptors [J].
Amendola, Valeria ;
Fabbrizzi, Luigi ;
Mosca, Lorenzo .
CHEMICAL SOCIETY REVIEWS, 2010, 39 (10) :3889-3915
[4]   Halogen bonding in solution: thermodynamics and applications [J].
Beale, Thomas M. ;
Chudzinski, Michael G. ;
Sarwar, Mohammed G. ;
Taylor, Mark S. .
CHEMICAL SOCIETY REVIEWS, 2013, 42 (04) :1667-1680
[5]   CRYSTALS version 12: software for guided crystal structure analysis [J].
Betteridge, PW ;
Carruthers, JR ;
Cooper, RI ;
Prout, K ;
Watkin, DJ .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2003, 36 :1487-1487
[6]   Strategies and Tactics for the Metal-Directed Synthesis of Rotaxanes, Knots, Catenanes, and Higher Order Links [J].
Beves, Jonathon E. ;
Blight, Barry A. ;
Campbell, Christopher J. ;
Leigh, David A. ;
McBurney, Roy T. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (40) :9260-9327
[7]   ortho-Phenylenediamine bis-urea-carboxylate:: a new reliable supramolecular synthon [J].
Brooks, SJ ;
Gale, PA ;
Light, ME .
CRYSTENGCOMM, 2005, 7 :586-591
[8]  
Bruker, 2007, APEX2
[9]   Applications of Supramolecular Anion Recognition [J].
Busschaert, Nathalie ;
Caltagirone, Claudia ;
Van Rossom, Wim ;
Gale, Philip A. .
CHEMICAL REVIEWS, 2015, 115 (15) :8038-8155
[10]   An anion-binding fluorinated alcohol isophthalamide isostere [J].
Busschaert, Nathalie ;
Jaramillo-Garcia, Javier ;
Light, Mark E. ;
Herniman, Julie ;
Langley, G. John ;
Gale, Philip A. .
RSC ADVANCES, 2014, 4 (11) :5389-5393