3'-acetylene-phenylene-acetylene spacer were prepared fromBINOL 1. The high optical rotation value and CD spectra demonstrated the main chain chirality of the oligomer molecule.The UV-VIS and fluorescent spectra evidence the characteristics of conjugated structure. In comparison with oligomer 2bearing 3
3'-acetylene spacer
the oligomers 3 and 7 have longer efficient conjugation segment
and their fluorescent quantumyields (φ) increased (0.60-0.65 versus 0.14).Extending the effective conjugation segment would improve the photophysical properties of chiral conjugated polymers.
Abstract
The 1
1'-binaphthol based oligomers 3 and 7 with 3
3'-acetylene-phenylene-acetylene spacer were prepared fromBINOL 1. The high optical rotation value and CD spectra demonstrated the main chain chirality of the oligomer molecule.The UV-VIS and fluorescent spectra evidence the characteristics of conjugated structure. In comparison with oligomer 2bearing 3
3'-acetylene spacer
the oligomers 3 and 7 have longer efficient conjugation segment
and their fluorescent quantumyields (φ) increased (0.60-0.65 versus 0.14).Extending the effective conjugation segment would improve the photophysical properties of chiral conjugated polymers.
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