Preorganized structures suitable for anion binding were prepared by introducing dipyrrolyldiketone BF2 complexes as acyclic anion-responsive pi-electronic molecules into macrocycles. Pyrrole-inverted conformations, which typically present low stability in the case of acyclic derivatives, were obtained by covalent linkages through ring-closing olefin metathesis, exhibiting extremely high affinity for different anions.
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NAIST, Grad Sch Mat Sci, Ikoma 6300192, JapanRitsumeikan Univ, Coll Pharmaceut Sci, Kusatsu 5258577, Japan
Shibaguchi, Hiroshi
Kawai, Tsuyoshi
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NAIST, Grad Sch Mat Sci, Ikoma 6300192, JapanRitsumeikan Univ, Coll Pharmaceut Sci, Kusatsu 5258577, Japan
Kawai, Tsuyoshi
Naito, Masanobu
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NAIST, Grad Sch Mat Sci, Ikoma 6300192, Japan
NIMS, Environm & Energy Mat Div, Tsukuba, Ibaraki 3054047, JapanRitsumeikan Univ, Coll Pharmaceut Sci, Kusatsu 5258577, Japan
Naito, Masanobu
Takaishi, Kazuto
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RIKEN, Adv Elements Chem Res Team, Wako, Saitama 3510198, Japan
RIKEN, Elements Chem Lab, Wako, Saitama 3510198, Japan
Seikei Univ, Fac Sci & Technol, Musashino, Tokyo 1808633, JapanRitsumeikan Univ, Coll Pharmaceut Sci, Kusatsu 5258577, Japan
Takaishi, Kazuto
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Uchiyama, Masanobu
Muranaka, Atsuya
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机构:
RIKEN, Adv Elements Chem Res Team, Wako, Saitama 3510198, Japan
RIKEN, Elements Chem Lab, Wako, Saitama 3510198, Japan
Japan Sci & Technol Agcy JST, PRESTO, Kawaguchi, Saitama 3320012, JapanRitsumeikan Univ, Coll Pharmaceut Sci, Kusatsu 5258577, Japan