MISC

2008年6月

Photophysical properties of oligophenylene ethynylenes modified by donor and/or acceptor groups

JOURNAL OF PHYSICAL CHEMISTRY A
  • Yoshihiro Yamaguchi
  • ,
  • Yukihiro Shimoi
  • ,
  • Takanori Ochi
  • ,
  • Tateaki Wakamiya
  • ,
  • Yoshio Matsubara
  • ,
  • Zen-ichi Yoshida

112
23
開始ページ
5074
終了ページ
5084
記述言語
英語
掲載種別
DOI
10.1021/jp7113219
出版者・発行元
AMER CHEMICAL SOC

To create highly fluorescent organic compounds in longer wavelength regions, and to gain physical chemistry insight into the photophysical characteristics, we investigated photophysical properties (Phi(f), lambda(em), tau, lambda(abs), epsilon, k(r), and k(d)) and their controlling factor dependence of the following pi-conjugated molecular rods consisting of p-phenyleneethynylene units modified by donor (OMe) and/or acceptor (CN): (1) side-donor modification systems (SD systems), (2) side-acceptor modification systems (SA systems), and (3) systems consisting of donor block and acceptor block (BL systems). As a result, very high Phi(f) values (> 0.95) were obtained for BL systems. Bathochromic shifts of lambda(em) in the same pi conjugation length were largest for BL systems. Thus we succeeded in the creation of highly efficient light emitters in the longer wavelength region by block modification (e.g., Phi(f) = 0.97, lambda(em) = 464 nm for BL-9), contrary to expectation from energy gap law. Considerably intense solid emission (Phi(f) similar to 0.5) in the longer wavelength region (500-560 nm) was also found for BL systems, presumably because of molecular orientation that hinders the self-quenching of fluorescence in solids. From (1) a Lippert-Mataga plot, (2) density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations, and (3) the positive linear relationship between the optical transition energy (nu(em)) and the difference between the highest occupied. molecular orbital of the donor and the lowest unoccupied molecular orbital of the acceptor (HOMO(D)-LUMO(A) difference), it is elucidated that the excited singlet (S-1) state of BL systems has a high charge transfer nature. The number (n) of energetically equivalent dipolar structure (EEDS) units in the oligoarylene ethynylenes is shown to be a measure of the effective pi conjugation length in the S-1 state. The S-1 state planarity increases with n values of EEDS units and by the introduction of donor and/or acceptor groups. It is worth noting that the Phi(f) values increase linearly with the n values of EEDS units.

リンク情報
DOI
https://doi.org/10.1021/jp7113219
CiNii Articles
http://ci.nii.ac.jp/naid/80019613062
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/18491882
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000256492200009&DestApp=WOS_CPL
ID情報
  • DOI : 10.1021/jp7113219
  • ISSN : 1089-5639
  • CiNii Articles ID : 80019613062
  • PubMed ID : 18491882
  • Web of Science ID : WOS:000256492200009

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