期刊
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2015, 期 35, 页码 7756-7762出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201501181
关键词
Luminescence; Cyclophanes; Chirality; Conjugation
资金
- Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan [15H00992]
- Japan Society for the Promotion of Science [14J02514]
- Grants-in-Aid for Scientific Research [15H00992, 14J02514] Funding Source: KAKEN
Optically active X-shaped dimers based on the planar chiral [2.2]paracyclophane have been synthesized. The dimers consist of stacked p-arylene-ethynylenes with phenyl, naphthyl, and anthryl groups as terminal units. The optical and chiroptical properties of the dimers and the corresponding model compounds were investigated. The naphthalene-containing dimer exhibits an intense circularly polarized luminescence (CPL) signal with a high dissymmetry factor (g(lum)) in the order of 10(-3) in addition to a high E and good photoluminescence quantum efficiency, which indicates that this compound is a highly emissive CPL material.
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