Red colored CPL emission of chiral 1,2-DACH-based polymers via chiral transfer of the conjugated chain backbone structure

2015 ◽  
Vol 6 (38) ◽  
pp. 6802-6805 ◽  
Author(s):  
Fei Li ◽  
Yuxiang Wang ◽  
Ziyu Wang ◽  
Yixiang Cheng ◽  
Chengjian Zhu

Chiral polymers incorporating a chiral 1,2-DACH moiety and BODIPY can exhibit strong mirror image Cotton effects and emit red colored CPL signals via the effective chiral transfer of the conjugated polymer chain backbone.


RSC Advances ◽  
2015 ◽  
Vol 5 (128) ◽  
pp. 105851-105854 ◽  
Author(s):  
Fei Li ◽  
Yuxiang Wang ◽  
Yuan Sheng ◽  
Guo Wei ◽  
Yixiang Cheng ◽  
...  

Chiral BINOL-based polymers incorporating phenothiazine moieties can exhibit strong mirror image Cotton effects and emit green color CPL signals via effective chiral transfer of the conjugated polymer chain backbone.



2001 ◽  
Vol 87 (8) ◽  
Author(s):  
T. Guillet ◽  
J. Berréhar ◽  
R. Grousson ◽  
J. Kovensky ◽  
C. Lapersonne-Meyer ◽  
...  


2002 ◽  
Vol 66 (11) ◽  
Author(s):  
F. Dubin ◽  
J. Berréhar ◽  
R. Grousson ◽  
T. Guillet ◽  
C. Lapersonne-Meyer ◽  
...  


2009 ◽  
Vol 159 (9-10) ◽  
pp. 805-808 ◽  
Author(s):  
Sadahiro Masuo ◽  
Tomoya Tanaka ◽  
Takumi Murakami ◽  
Akito Masuhara ◽  
Shinjiro Machida ◽  
...  


2009 ◽  
Vol 94 (18) ◽  
pp. 183109
Author(s):  
B. Mondal ◽  
D. Majumdar ◽  
A. Ghosh ◽  
S. K. Saha


2013 ◽  
Vol 5 (18) ◽  
pp. 9043-9050 ◽  
Author(s):  
Seok-Ju Kang ◽  
Youn-Su Kim ◽  
Won Bae Kim ◽  
Dong-Yu Kim ◽  
Yong-Young Noh


2007 ◽  
Vol 5 (4) ◽  
pp. 923-930
Author(s):  
Alexander Kuehne ◽  
Allan Mackintosh ◽  
David Armstrong ◽  
Richard Pethrick

AbstractPoly(9,9-dioctylfluorene) (PFO) shows highly efficient blue emission with photo excitation occurring between 340–400 nm. Here we show that PFO can in dilute solution emit at a wavelength well below that at which it is being exited. This, we propose is related to an energy transfer from conjugated parts of the polymer chain into more localised states which then emit at a lower wavelength. These localised states can be considered as defects in the conjugation of the polymer or as chain ends. These may produce quasi monomer or quasi dimer species within the chain, which will have a HOMO-LUMO gap of higher energy than the conjugated polymer. These then fluoresce at the lower wavelength; essentially causing, by energy transfer, a process of energy up-conversion.



2012 ◽  
Vol 706-709 ◽  
pp. 1636-1641 ◽  
Author(s):  
Takashi Hirahara ◽  
Masahiro Yoshizawa-Fujita ◽  
Yuko Takeoka ◽  
Masahiro Rikukawa

Fluorene-thiophene copolymers having chiral and azobenzene substituents, PAzB4-T, were synthesized by the Pd-catalyzed Suzuki coupling method. We studied the aligning organization of the main chain of PAzB4-T with the activation of the attached functional groups by thermal annealing and photo-annealing processes. Circular dichroism (CD) measurements revealed that the thermally annealed PAzB4-T spin-coated films exhibited bisignate Cotton effects over the absorption regions of the polymer main chains and the azobenzene side chains due to the formation of chiral assemblies. After the photo-annealing process, which means linearly polarized light irradiation accompanied by thermal annealing, the PAzB4-T spin-coated films showed linear dichroism over the absorption region of the main chains, due to the alignment of azobenzene side chains against the electric field of the linearly polarized light. These results suggested that rigid conjugated polymers were successfully aligned by the alignment of functional groups with the external stimuli.



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