日本語
 
Help Privacy Policy ポリシー/免責事項
  詳細検索ブラウズ

アイテム詳細


公開

学術論文

Unraveling unidirectional threading of α-cyclodextrin in a [2]rotaxane through spin labeling approach.

MPS-Authors
/persons/resource/persons32653

Pievo,  R.
Research Group of Electron Spin Resonance Spectroscopy, MPI for biophysical chemistry, Max Planck Society;

External Resource
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
フルテキスト (公開)

1569437.pdf
(出版社版), 577KB

1569437_si_001.pdf
(出版社版), 956KB

付随資料 (公開)
There is no public supplementary material available
引用

Casati, C., Franchi, P., Pievo, R., Mezzina, E., & Lucarini, M. (2012). Unraveling unidirectional threading of α-cyclodextrin in a [2]rotaxane through spin labeling approach. Journal of the American Chemical Society, 134(46), 19108-19117. doi:10.1021/ja3073484.


引用: https://hdl.handle.net/11858/00-001M-0000-0010-21CA-A
要旨
We present here the results of a CW-ESR investigation of a double spin labeled α-cyclodextrin-based [2]rotaxane that is characterized by the presence of nitroxide labels both at the wheel and at the dumbbell. This was accomplished by synthesizing a spin labeled α-CD (the wheel) that was mechanically blocked on a thread containing a nitroxide unit by a Cu(I) catalyzed azide–alkyne cycloaddition (CuAAC). Both ESI-MS analysis and NMR spectroscopy were used to provide evidence of the threading processes. Because of the unsymmetrical structure of both the wheel and the axle, two different geometrical isomers could be predicted on the basis of the orientation of the CD along the thread. By combining molecular dynamic calculations and information extracted from the CW-ESR spectra, we were able to determine the geometrical nature of the isomer that was isolated as the only species. The ESR spectra showed J-coupling between the two mechanically connected nitroxide units and were analyzed by a model assuming three main molecular states. The intramolecular noncovalent nature of spin exchange was confirmed by reversibly switching the magnetic interaction on–off by changing the pH of the solution in the presence of a competing macrocyclic host.