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2. Novel 1,8-Naphthalimide derivative with an open space for an anion: Unique fluorescence behaviour depending on the binding anion’s electrophilic property

Author

Izawa, Hironori, Nishino, Shoji, Sumita, Masato, Akamatsu, Masaaki, Morihashi, Kenji, Ifuku, Shinsuke, Morimoto, Minoru, Saimoto, Hiroyuki, Izawa, Hironori, Nishino, Shoji, Sumita, Masato, Akamatsu, Masaaki, Morihashi, Kenji, Ifuku, Shinsuke, Morimoto, Minoru, and Saimoto, Hiroyuki

Abstract

We have designed a novel 1,8-naphthalimide derivative with an open space for an anion. Computational calculation has predicted that the space could trap various anion species and photo-induced charge transfer depending on the anion's electrophilic properties. Indeed, the fluorescence behaviour of the 1,8-naphthalimide derivative complexes with each anion is consistent with the computational prediction.

Published
2019

4. Novel 1,8-Naphthalimide derivative with an open space for an anion: Unique fluorescence behaviour depending on the binding anion’s electrophilic property

Author

Izawa, Hironori, Nishino, Shoji, Sumita, Masato, Akamatsu, Masaaki, Morihashi, Kenji, Ifuku, Shinsuke, Morimoto, Minoru, Saimoto, Hiroyuki, Izawa, Hironori, Nishino, Shoji, Sumita, Masato, Akamatsu, Masaaki, Morihashi, Kenji, Ifuku, Shinsuke, Morimoto, Minoru, and Saimoto, Hiroyuki

Abstract

We have designed a novel 1,8-naphthalimide derivative with an open space for an anion. Computational calculation has predicted that the space could trap various anion species and photo-induced charge transfer depending on the anion's electrophilic properties. Indeed, the fluorescence behaviour of the 1,8-naphthalimide derivative complexes with each anion is consistent with the computational prediction.

Published
2015

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