TY - JOUR
T1 - Multicomponent molecular puzzles for photofunction design
T2 - Emission color variation in lewis acid-base pair crystals coupled with guest-to-host charge transfer excitation
AU - Ono, Toshikazu
AU - Sugimoto, Manabu
AU - Hisaeda, Yoshio
N1 - Publisher Copyright:
© 2015 American Chemical Society.
PY - 2015/8/5
Y1 - 2015/8/5
N2 - Simple yet ubiquitous multimolecular assembly systems with color-tunable emissions are realized by cooperative electron donor-acceptor interactions, such as the boron-nitrogen (B-N) dative bond as a Lewis acid-base pair and charge transfer (CT) interactions. These are ternary-component systems consisting of a naphthalenediimide derivative (NDI), tris(pentafluorophenyl)borane (TPFB), and aromatic molecules (guest) with an NDI:TPFB:guest ratio of 1:2:2. The crystal shows guest-dependent color-tunable emissions such as deep blue to orange when a guest molecule of benzene is replaced with other conjugated systems. A good correlation between the emission wavelength and ionization potential of the guest and electronic structure calculations indicated that the emission is due to the CT transition from the guest to the NDI. The present study suggests that a rational solution of multcomponent molecular puzzles would be useful for obtaining novel photofunctional solid-state systems.
AB - Simple yet ubiquitous multimolecular assembly systems with color-tunable emissions are realized by cooperative electron donor-acceptor interactions, such as the boron-nitrogen (B-N) dative bond as a Lewis acid-base pair and charge transfer (CT) interactions. These are ternary-component systems consisting of a naphthalenediimide derivative (NDI), tris(pentafluorophenyl)borane (TPFB), and aromatic molecules (guest) with an NDI:TPFB:guest ratio of 1:2:2. The crystal shows guest-dependent color-tunable emissions such as deep blue to orange when a guest molecule of benzene is replaced with other conjugated systems. A good correlation between the emission wavelength and ionization potential of the guest and electronic structure calculations indicated that the emission is due to the CT transition from the guest to the NDI. The present study suggests that a rational solution of multcomponent molecular puzzles would be useful for obtaining novel photofunctional solid-state systems.
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U2 - 10.1021/jacs.5b04178
DO - 10.1021/jacs.5b04178
M3 - Article
AN - SCOPUS:84938853338
SN - 0002-7863
VL - 137
SP - 9519
EP - 9522
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 30
ER -