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Open AccessCommunication

Effects of Substituents on the Blue Luminescence of Disilane-Linked Donor‒Acceptor‒Donor Triads

1
Department of Chemistry, School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan
2
Division of Physics, Faculty of Pure and Applied Sciences, Tsukuba Research Center for Interdisciplinary Materials Science (TIMS), and Center for Integrated Research in Fundamental Science and Engineering (CiRfSE), University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8571, Japan
*
Authors to whom correspondence should be addressed.
Academic Editor: Mitsuo Kira
Molecules 2019, 24(3), 521; https://doi.org/10.3390/molecules24030521
Received: 28 December 2018 / Revised: 22 January 2019 / Accepted: 29 January 2019 / Published: 31 January 2019
(This article belongs to the Special Issue Advances in Silicon Chemistry 2018)
A series of disilane-linked donor‒acceptor‒donor triads (D‒Si‒Si‒A‒Si‒Si‒D) was synthesized to investigate the effects of substituents on the photophysical properties. The triads were prepared by metal-catalyzed diiodosilylation of aryl iodides using a Pd(P(t-Bu)3)2/(i-Pr)2EtN/toluene system that we previously developed. Optical measurements, X-ray diffraction analysis, and density functional theory calculations revealed relationships between the photophysical properties and molecular structures of these triads in solution and in the solid state. The compounds emitted blue to green fluorescence in CH2Cl2 solution and in the solid state. Notably, compound 2 showed fluorescence with an absolute quantum yield of 0.17 in the solid state but showed no fluorescence in CH2Cl2. Our findings confirmed that the substituent adjacent to the disilane moiety affects the conformations and emission efficiencies of compounds in solution and in the solid state. View Full-Text
Keywords: disilane; donor‒acceptor; optical properties; solid-state emission; X-ray diffraction; DFT calculation disilane; donor‒acceptor; optical properties; solid-state emission; X-ray diffraction; DFT calculation
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MDPI and ACS Style

Usuki, T.; Omoto, K.; Shimada, M.; Yamanoi, Y.; Kasai, H.; Nishibori, E.; Nishihara, H. Effects of Substituents on the Blue Luminescence of Disilane-Linked Donor‒Acceptor‒Donor Triads. Molecules 2019, 24, 521. https://doi.org/10.3390/molecules24030521

AMA Style

Usuki T, Omoto K, Shimada M, Yamanoi Y, Kasai H, Nishibori E, Nishihara H. Effects of Substituents on the Blue Luminescence of Disilane-Linked Donor‒Acceptor‒Donor Triads. Molecules. 2019; 24(3):521. https://doi.org/10.3390/molecules24030521

Chicago/Turabian Style

Usuki, Tsukasa; Omoto, Kenichiro; Shimada, Masaki; Yamanoi, Yoshinori; Kasai, Hidetaka; Nishibori, Eiji; Nishihara, Hiroshi. 2019. "Effects of Substituents on the Blue Luminescence of Disilane-Linked Donor‒Acceptor‒Donor Triads" Molecules 24, no. 3: 521. https://doi.org/10.3390/molecules24030521

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