Tunable Circularly Polarized Luminescence of Helical Poly(phenylacetylene)s via Side-chain-to-Backbone Förster Resonance Energy Transfer
RESEARCH ARTICLE|Updated:2026-08-03
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Tunable Circularly Polarized Luminescence of Helical Poly(phenylacetylene)s via Side-chain-to-Backbone Förster Resonance Energy Transfer
Chinese Journal of Polymer ScienceVol. 44, Pages: 1-9(2026)
Affiliations:
Beijing National Laboratory for Molecular Science, Key Laboratory of Polymer Chemistry and Physics of the Ministry of Education, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China
Huang, Y. H.; Guan, J.; Yu, J. Q.; Wan, X. H.; Zhang, J. Tunable circularly polarized luminescence of helical poly(phenylacetylene)s via side-chain-to-backbone förster resonance energy transfer. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3795-2
Yi-Han Huang, Jian Guan, Jia-Qi Yu, et al. Tunable Circularly Polarized Luminescence of Helical Poly(phenylacetylene)s via Side-chain-to-Backbone Förster Resonance Energy Transfer[J/OL]. Chinese Journal of Polymer Science, 2026, 441-9. DOI: 10.1007/s10118-026-3795-2.
Huang, Y. H.; Guan, J.; Yu, J. Q.; Wan, X. H.; Zhang, J. Tunable circularly polarized luminescence of helical poly(phenylacetylene)s via side-chain-to-backbone förster resonance energy transfer. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3795-2DOI:
Yi-Han Huang, Jian Guan, Jia-Qi Yu, et al. Tunable Circularly Polarized Luminescence of Helical Poly(phenylacetylene)s via Side-chain-to-Backbone Förster Resonance Energy Transfer[J/OL]. Chinese Journal of Polymer Science, 2026, 441-9. DOI: 10.1007/s10118-026-3795-2.DOI:
Tunable Circularly Polarized Luminescence of Helical Poly(phenylacetylene)s via Side-chain-to-Backbone Förster Resonance Energy Transfer
yet their color tunability and light-harvesting capability remain limited because the emission mainly originates from the backbone excited states. Herein
we construct side-chain/backbone bichromophoric PPA systems to investigate Förster resonance energy transfer (FRET) and its effect on CPL performance. Using a pentafluorophenyl ester-functionalized
PPA-PFP
as a common precursor
planar aromatic donors
pyrene (Py) and naphthalene (Nap)
and a non-coplanar donor
triphenylamine (TPA)
were systematically introduced through activated-ester amidation.
Py-PPA
and
Nap-PPA
both underwent efficient donor-to-backbone energy transfer to the emissive
cis-cisoid
helical backbone
while
Py-PPA
showed a higher FRET efficiency and a much more pronounced solid-state CPL enhancement
with a |
g
lum
| value of 7×10
−2
in the film. In c
ontrast
TPA-PPA
exhibited conformation-coupled FRET attenuation and emission color switching because the bulky twisted donor destabilized the
cis-cisoid
backbone. Further spectroscopic and diffraction studies revealed that the superior CPL performance of
Py-PPA
originated from the synergistic combination of stronger pendant chiral ordering and more efficient side-chain-to-backbone energy transfer during solution aging and film formation. These results show that donor-pendant modification is an effective way to regulate FRET and CPL in intrinsically emissive PPA systems.
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Keywords
references
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