Abstract
The complexation behavior of a series of electron donor-accepter (D-A) covalently linked compounds with cyclodextrins (CyDs) has been reviewed. The structure of these complexes showed rotaxane type conformations, which were investigated by means of 1H NMR spectrometry. The complex formations induced a fixation of a conformation of guest D-A molecules, and D-A distances were enlarged. Thus, accurate photo-induced charge transfer behaviors can be discussed.
| Original language | English |
|---|---|
| Pages (from-to) | 105-110 |
| Number of pages | 6 |
| Journal | Journal of Inclusion Phenomena |
| Volume | 50 |
| Issue number | 1-2 |
| Publication status | Published - Oct 1 2004 |
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All Science Journal Classification (ASJC) codes
- Food Science
- Chemistry(all)
- Condensed Matter Physics
Cite this
Rotaxane type complexation behavior of cyclodextrins with a series of donor-acceptor covarently linked compounds. / Morozumi, Tatsuya; Kimura, Takashi; Ujiie, Tomomi; Yonemura, Hiroaki; Matsuo, Taku; Nakamura, Hiroshi.
In: Journal of Inclusion Phenomena, Vol. 50, No. 1-2, 01.10.2004, p. 105-110.Research output: Contribution to journal › Article
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TY - JOUR
T1 - Rotaxane type complexation behavior of cyclodextrins with a series of donor-acceptor covarently linked compounds
AU - Morozumi, Tatsuya
AU - Kimura, Takashi
AU - Ujiie, Tomomi
AU - Yonemura, Hiroaki
AU - Matsuo, Taku
AU - Nakamura, Hiroshi
PY - 2004/10/1
Y1 - 2004/10/1
N2 - The complexation behavior of a series of electron donor-accepter (D-A) covalently linked compounds with cyclodextrins (CyDs) has been reviewed. The structure of these complexes showed rotaxane type conformations, which were investigated by means of 1H NMR spectrometry. The complex formations induced a fixation of a conformation of guest D-A molecules, and D-A distances were enlarged. Thus, accurate photo-induced charge transfer behaviors can be discussed.
AB - The complexation behavior of a series of electron donor-accepter (D-A) covalently linked compounds with cyclodextrins (CyDs) has been reviewed. The structure of these complexes showed rotaxane type conformations, which were investigated by means of 1H NMR spectrometry. The complex formations induced a fixation of a conformation of guest D-A molecules, and D-A distances were enlarged. Thus, accurate photo-induced charge transfer behaviors can be discussed.
UR - http://www.scopus.com/inward/record.url?scp=12344313094&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=12344313094&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:12344313094
VL - 50
SP - 105
EP - 110
JO - Journal of Inclusion Phenomena and Macrocyclic Chemistry
JF - Journal of Inclusion Phenomena and Macrocyclic Chemistry
SN - 1388-3127
IS - 1-2
ER -