Shape-persistent macrocycles - Self-assembly reactions and characterization by hyperpolarized 129Xe NMR spectroscopy

被引:4
|
作者
Campbell, Katie [1 ]
Ooms, Kristopher J. [1 ]
Ferguson, Michael J. [1 ]
Stang, Peter J. [3 ]
Wasylishen, Roderick E. [1 ]
Tykwinski, Rik R. [1 ,2 ]
机构
[1] Univ Alberta, Dept Chem, Edmonton, AB T6G 2G2, Canada
[2] Univ Erlangen Nurnberg, Inst Organ Chem, D-91054 Erlangen, Germany
[3] Univ Utah, Dept Chem, Salt Lake City, UT 84112 USA
基金
加拿大自然科学与工程研究理事会;
关键词
macrocycles; solid-state NMR; supramolecular chemistry; xenon NMR; porous solids; metal-organic framework; NUCLEAR-MAGNETIC-RESONANCE; METAL-ORGANIC FRAMEWORKS; BUILDING-BLOCKS; SUPRAMOLECULAR CHEMISTRY; MICROPOROUS SOLIDS; CONTINUOUS-FLOW; CHEMICAL-SHIFT; LINE-SHAPES; COORDINATION POLYMERS; CRYSTAL-STRUCTURE;
D O I
10.1139/V11-077
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The use of three shape-persistent, conjugated macrocycles 2a-2c as ligands for self-assembly reactions is described. The macrocycles have been characterized through a combination of spectroscopic analyses and, for compounds 2b and 2c, X-ray crystallographic analysis. Whereas the reaction of 2a with the cis-Pt(II) species 3 successfully provides the porous solid 4a, the analogous reaction of 2b and 2c with 3 leads only to mixtures of products. The application of continuous-flow hyperpolarized Xe-129 NMR spectroscopy to investigate the solid-state pores of macrocycles 2b and 2c and the supramolecular complex 4a as a function of temperature is described. All three species show permanent porosity upon removal of co-crystallized solvent molecules. Using trends in the Xe-129 chemical shifts and temperature-dependent dynamics of Xe atoms in the solids, information is obtained on the nature of the pores in these systems. Using the Xe-129 NMR data for complex 4a, the effective heat of adsorption (Delta Hads) was calculated to be similar to 29 kJ mol(-1).
引用
收藏
页码:1264 / 1276
页数:13
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