講演会のお知らせ repurposing aromaticity for …講演会のお知らせ repurposing...

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講演会のお知らせ Repurposing Aromaticity for Organic Electronics: Making, Breaking and Stacking π -Circuits Prof. Dr. J. D. Tovar 日時:1 月 31 日 (木) 15:30 ~ 場所:R1棟 第1会議室 連絡先:福島孝典 (5220) Department of Chemistry, Johns Hopkins University ABST CT: Several emerging energy technologies require exible and solution-processable organic-based electronic materials capable of speci c degrees of energy transport in order to achieve desired functions. e range of materials (and applications) is quite diverse, as exempli ed by new materials that can facilitate photovoltaic, light emi ing or transistor behavior. e molecular requirements necessary to achieve these functions vary greatly, and this lecture will highlight two fundamental structural considerations relevant to the design of materials that can foster or otherwise regulate e cient energy/ charge migration. One aspect involves the use of unusual aromatic building blocks with relatively low degrees of resonance stabilization that can encourage intramolecular electronic delocalization. ese types of molecules can foster di erent types of “quantum interference” tunable through anion binding and can display uxional aromatic properties that support diradical character. Another aspect involves the control of intermolecular electronic delocalization through the use of water-soluble oligopeptides a ached to pi-conjugated oligomers that self-assemble into brillar bioelectronic nanostructures containing internal pi-stacked electronic conduits. is platform enables peptidic energy transport in completely aqueous environments of high ionic strength. In both aspects, the making, breaking and stacking of aromatic rings plays a critical role to de ne the physical properties of the materials and the possible arenas where they may be employed. KEY REFERENCES: (1) J. Am. Chem. Soc . 2017 , 139 , 8685–8692. (2) J. Org. Chem . 2017 , 82 , 13440–13448. (3) J. Am. Chem. Soc . 2016 , 138 , 3362-3370. (4) Angew. Chem. Int. Ed . 2015 , 54 , 5888–5893.

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Page 1: 講演会のお知らせ Repurposing Aromaticity for …講演会のお知らせ Repurposing Aromaticity for Organic Electronics: Making, Breaking and Stacking !-Circuits Prof. Dr

講演会のお知らせRepurposing Aromaticity for Organic Electronics:

Making, Breaking and Stacking π-Circuits Prof. Dr. J. D. Tovar

日時:1 月 31 日 (木) 15:30 ~場所:R1棟 第1会議室

連絡先:福島孝典 (5220)

Department of Chemistry, Johns Hopkins University

ABSTRACT:Several emerging energy technologies require flexible and solution-processable organic-based electronic materials capable of specific degrees of energy transport in order to achieve desired functions. The range of materials (and applications) is quite diverse, as exemplified by new materials that can facilitate photovoltaic, light emitting or transistor behavior. The molecular requirements necessary to achieve these functions vary greatly, and this lecture will highlight two fundamental structural considerations relevant to the design of materials that can foster or otherwise regulate efficient energy/charge migration. One aspect involves the use of unusual aromatic building blocks with relatively low degrees of resonance stabilization that can encourage intramolecular electronic delocalization. These types of molecules can foster different types of “quantum interference” tunable through anion binding and can display fluxional aromatic properties that support diradical character. Another aspect involves the control of intermolecular electronic delocalization through the use of water-soluble oligopeptides attached to pi-conjugated oligomers that self-assemble into fibrillar bioelectronic nanostructures containing internal pi-stacked electronic conduits. This platform enables peptidic energy transport in completely aqueous environments of high ionic strength. In both aspects, the making, breaking and stacking of aromatic rings plays a critical role to define the physical properties of the materials and the possible arenas where they may be employed. KEY REFERENCES: (1) J. Am. Chem. Soc. 2017, 139, 8685–8692. (2) J. Org. Chem. 2017, 82, 13440–13448. (3) J. Am. Chem. Soc. 2016, 138, 3362-3370. (4) Angew. Chem. Int. Ed. 2015, 54, 5888–5893.