TY - JOUR
T1 - Design and synthesis of dipyrrin complexes bearing unique structures, properties and functions
AU - Nabeshima, Tatsuya
AU - Yamamura, Masaki
AU - Richards, Gary J.
AU - Nakamura, Takashi
PY - 2015
Y1 - 2015
N2 - We first describe N2O2- type dipyrrins, which behave as tridentate or tetradentate ligands for the preparation of main- group- element complexes including B, Al, Si, Ge, and Sn. Similar complexes were unstable or hard to prepare using usual bidentate dipyrrins. In particular, the stable hypercoordinate dipyrrin- silicon complexes showed interconvertible photo- optical properties. The Ge and Sn complexes were obtained in a similar way. Ar,O - BODIPYs were also synthesized from the N2O2- type dipyrrins. Their application to a light harvesting molecular assembly is also shown. Second, we demonstrate the usefulness and potential of dipyrrin complexes in supramolecular chemistry. The one-, two- and three- dimensional supramolecular architectures are available because multidentate dipyrrin derivatives can be easily obtained through chemical modifications of the dipyrrin skeleton. Last we describe the binding ability of the fluorine atoms in BODIPY to cationic guests to create a functional response to an external stimulus.
AB - We first describe N2O2- type dipyrrins, which behave as tridentate or tetradentate ligands for the preparation of main- group- element complexes including B, Al, Si, Ge, and Sn. Similar complexes were unstable or hard to prepare using usual bidentate dipyrrins. In particular, the stable hypercoordinate dipyrrin- silicon complexes showed interconvertible photo- optical properties. The Ge and Sn complexes were obtained in a similar way. Ar,O - BODIPYs were also synthesized from the N2O2- type dipyrrins. Their application to a light harvesting molecular assembly is also shown. Second, we demonstrate the usefulness and potential of dipyrrin complexes in supramolecular chemistry. The one-, two- and three- dimensional supramolecular architectures are available because multidentate dipyrrin derivatives can be easily obtained through chemical modifications of the dipyrrin skeleton. Last we describe the binding ability of the fluorine atoms in BODIPY to cationic guests to create a functional response to an external stimulus.
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U2 - 10.5059/yukigoseikyokaishi.73.1111
DO - 10.5059/yukigoseikyokaishi.73.1111
M3 - Article
AN - SCOPUS:84959287117
SN - 0037-9980
VL - 73
SP - 1111
EP - 1119
JO - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
JF - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
IS - 11
ER -