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Effect of the position of substitution on the electronic properties of nitrophenyl derivatives of fulleropyrrolidines:Fundamental understanding toward raising LUMO energy of fullerene electron-acceptor 被引量:3

Effect of the position of substitution on the electronic properties of nitrophenyl derivatives of fulleropyrrolidines:Fundamental understanding toward raising LUMO energy of fullerene electron-acceptor
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摘要 A series of substituted para-, meta- and ortho-nitrophenyl derivatives of fulleropyrrolidine were synthesized to investigate the effects of the position of substitution on electronic properties by using steady-state absorption and fluorescence spectra, combined with DFT calculations. The results confirmed that the position of substitution has little effect on absorption and fluorescence spectra, whereas a significant effect was observed on their LUMO energy levels. The theoretical calculations revealed that the LUMO energy of the ortho-nitrophenyl substituted derivative was increased 0.1 eV above those ofpara- and meta-substitution. The prominent effect ofortho-substitution was attributed to the through-space orbital interaction between spatially closed electron-withdrawing nitro group and fullerene cage. These findings could provide fundamental insights in raising LUMO levels of C6o-based electron acceptor materials and an alternative strategy to increase open circuit voltage Voc in polymer solar cells. A series of substituted para-, meta- and ortho-nitrophenyl derivatives of fulleropyrrolidine were synthesized to investigate the effects of the position of substitution on electronic properties by using steady-state absorption and fluorescence spectra, combined with DFT calculations. The results confirmed that the position of substitution has little effect on absorption and fluorescence spectra, whereas a significant effect was observed on their LUMO energy levels. The theoretical calculations revealed that the LUMO energy of the ortho-nitrophenyl substituted derivative was increased 0.1 eV above those ofpara- and meta-substitution. The prominent effect ofortho-substitution was attributed to the through-space orbital interaction between spatially closed electron-withdrawing nitro group and fullerene cage. These findings could provide fundamental insights in raising LUMO levels of C6o-based electron acceptor materials and an alternative strategy to increase open circuit voltage Voc in polymer solar cells.
机构地区 College of Chemistry
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2014年第4期501-504,共4页 中国化学快报(英文版)
基金 supported by Shanghai Pujiang Program(No.11PJ1400200) Innovation Program of Shanghai Municipal Education Commission(No.12ZZ067) the Research Fund for the Doctoral Program of Higher Education of China the Fundamental Research Funds for the Central Universities
关键词 Fullerene Substituent effect Orbital interaction Organic photovoltaics Fullerene Substituent effect Orbital interaction Organic photovoltaics
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