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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Yamagata Univ, Grad Sch Organ Mat Sci, Dept Organ Mat Sci, Yonezawa, Yamagata 9928510, JapanYamagata Univ, Grad Sch Organ Mat Sci, Dept Organ Mat Sci, Yonezawa, Yamagata 9928510, Japan
Yamakado, Ryohei
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Hara, Mitsuo
Nagano, Shusaku
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Nagoya Univ, Venture Business Lab, Nagoya, Aichi 4648603, JapanYamagata Univ, Grad Sch Organ Mat Sci, Dept Organ Mat Sci, Yonezawa, Yamagata 9928510, Japan
Nagano, Shusaku
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Seki, Takahiro
Maeda, Hiromitsu
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Ritsumeikan Univ, Dept Appl Chem, Coll Life Sci, Kusatsu, Shiga 5258577, JapanYamagata Univ, Grad Sch Organ Mat Sci, Dept Organ Mat Sci, Yonezawa, Yamagata 9928510, Japan
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Oak Ridge Natl Lab, Div Mat Sci & Technol, Oak Ridge, TN 37831 USAOak Ridge Natl Lab, Div Mat Sci & Technol, Oak Ridge, TN 37831 USA
Zarkadoula, Eva
Toulemonde, Marcel
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Univ Caen, CEA CNRS ENSICAEN, Ctr Interdisciplinaire Rech Ions Matriaux & Photo, F-14070 Caen, FranceOak Ridge Natl Lab, Div Mat Sci & Technol, Oak Ridge, TN 37831 USA
Toulemonde, Marcel
Weber, William J.
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Oak Ridge Natl Lab, Div Mat Sci & Technol, Oak Ridge, TN 37831 USA
Univ Tennessee, Dept Mat Sci & Engn, Knoxville, TN 37996 USAOak Ridge Natl Lab, Div Mat Sci & Technol, Oak Ridge, TN 37831 USA