Please use this identifier to cite or link to this item: http://lib.jncasr.ac.in:8080/jspui/handle/10572/2139
Title: Tuning the HOMO energy levels in quinoline and biquinoline based donor-acceptor polymers
Authors: Tomar, Manisha
Ashar, A. Z.
Narayan, K. S.
Muellen, Klaus
Jacob, Josemon
Keywords: Polymer Science
Quinoline
Biquinoline
Donor-acceptor
Cyclopentadithiophene
2,1,3-benzothiadiazole
Optical properties
Heterojunction Solar-Cells
Band-Gap Polymers
Conjugated Polymers
Electrochemical Properties
Optoelectronic Properties
Organic Photovoltaics
Facile Synthesis
Copolymers
Systems
Electroluminescence
Issue Date: 2016
Publisher: Springer
Citation: Tomar, M.; Ashar, A. Z.; Narayan, K. S.; Mullen, K.; Jacob, J., Tuning the HOMO energy levels in quinoline and biquinoline based donor-acceptor polymers. Journal of Polymer Research 2016, 23 (3), 9 http://dx.doi.org/10.1007/s10965-016-0945-1
Journal of Polymer Research
23
3
Abstract: Four donor-acceptor type polymers based on quinoline and biquinoline have been synthesized by Pd catalyzed direct C-H (hetero)arylation reaction. Polymers P1 and P2 are alternate copolymers of thiophene-benzothiadiazole-thiophene (TBTT) unit with quinoline and biquinoline unit, respectively. P3 is a random copolymer containing cyclopentadithiophene (CPDT), benzothiadiazole and quinoline moieties in the backbone whereas P4 contains CPDT unit with randomly distributed benzothiadiazole and biquinoline units. All the polymers show good thermal stability and solubility in common organic solvents. CPDT based polymers P3 and P4 exhibit higher absorbance maxima, higher lying Highest Occupied Molecular Orbital (HOMO) energy levels and smaller band gap as compared to thiophene based polymers P1 and P2 as a result of better electron-donating ability of the former leading to stronger intramolecular charge transfer. Also, quinoline based polymers P1 and P3 show a redshift in the absorbance maxima compared to biquinoline based polymers P2 and P4, respectively due to non-planar transoid conformation of the two quinoline rings in the biquinoline unit. It is found that the use of N-heterocycle based comonomers allows the tuning of the HOMO level over a remarkably wide range (similar to 0.8 eV). Additionally, the use of quinoline or biquinoline along the conjugated chain leads to deeper lying HOMO levels suggesting good oxidative stability for this class of materials.
Description: Restricted Access
URI: http://hdl.handle.net/10572/2139
ISSN: 1022-9760
Appears in Collections:Research Articles (Narayan K. S.)

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