2015
DOI: 10.1007/s13233-015-3078-1
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Bathochromic shift in absorption spectra of conjugated polymer nanoparticles with displacement along backbones

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Cited by 35 publications
(14 citation statements)
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“…Such absorbance enhancement of the TIIG-Bz/2-BBA in the NIR region of the spectra was clearly shown even after excluding any scattering effect by measuring the spectra with an integrating sphere. The higher absorbance of the TIIG-Bz wires assembled with 2-BBA in the NIR region was consistent with our recent results of density functional theory calculations for conjugated polymer nanoparticles 54 , 55 . Such a red shift in the absorption spectra originates from enhanced intermolecular π − π interactions with energy level adjustments, and has been widely observed in thin films for organic optoelectronic devices or nanomaterials of conjugated polymers 56 61 .…”
Section: Resultssupporting
confidence: 91%
“…Such absorbance enhancement of the TIIG-Bz/2-BBA in the NIR region of the spectra was clearly shown even after excluding any scattering effect by measuring the spectra with an integrating sphere. The higher absorbance of the TIIG-Bz wires assembled with 2-BBA in the NIR region was consistent with our recent results of density functional theory calculations for conjugated polymer nanoparticles 54 , 55 . Such a red shift in the absorption spectra originates from enhanced intermolecular π − π interactions with energy level adjustments, and has been widely observed in thin films for organic optoelectronic devices or nanomaterials of conjugated polymers 56 61 .…”
Section: Resultssupporting
confidence: 91%
“…The absorption spectrum of the CPNs (Figure 1d) shows that the absorption maximum of the PCPDTBT assembled in the CPNs is significantly red-shifted to 796 nm in comparison to that of the PCPDTBT dissolved in the chloroform (717 nm). The 79 nm of bathochromic shift in the absorption spectrum was attributed to the intermolecular electronic delocalization between the backbones of the PCPDTBT in the CPNs, as demonstrated in the films and PCPDTBT films and nanoparticles used for the photovoltaic cell and biomedical fields [33,34,35]. This result indicates that the PCPDTBT backbones are closely associated in CPNs, resulting in a prominent enhancement in NIR absorption.…”
Section: Resultsmentioning
confidence: 90%
“…The bathochromic shift can be a result of the interaction of the aromatic motifs due to their spatial proximity, hydrogen bonding between the benzothiadiazole and the newly generated hydroxyl groups, as well as a polarity change of the surrounding environment upon conjugation. 57–59 The introduction of the azide groups was performed with the crude solution containing the copolymer epoxidized by m CPBA. Similarly, sodium azide was dissolved in DMF and added to the epoxide-containing solution.…”
Section: Resultsmentioning
confidence: 99%