Stereogenic cyclic oligonaphthalenes displaying ring size-dependent handedness of circularly polarized luminescence (CPL)
A series of cyclic oligomers with Dn symmetry (n = 2-5) based on chiral (R)/(S)-binaphthyl exhibiting intensive chiroptical properties were synthesized by using a Ni(0)-catalyzed coupling reaction. The intensity and the handedness of circularly polarized luminescence (CPL) were dependent on the ring...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2019-02, Vol.55 (19), p.2749-2752 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A series of cyclic oligomers with Dn symmetry (n = 2-5) based on chiral (R)/(S)-binaphthyl exhibiting intensive chiroptical properties were synthesized by using a Ni(0)-catalyzed coupling reaction. The intensity and the handedness of circularly polarized luminescence (CPL) were dependent on the ring size of the cyclic oligomers, in which the 1,1'-binaphthyl moieties form s-cis (n = 2, 3) or s-trans (n = 4, 5) conformers in the excited state. The relationship between the structure and chiroptical properties is discussed with the aid of X-ray analysis and DFT calculations. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c8cc08929a |