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Photophysical property, electronic structure and solid-state packing of O-heterocyclic annulated perylene diimide

Wenjing Li (School of Municipal and Environmental Engineering, Shandong Jianzhu University, Jinan, China)
Qi Wang (School of Municipal and Environmental Engineering, Shandong Jianzhu University, Jinan, China)
Yongshan Ma (School of Municipal and Environmental Engineering, Shandong Jianzhu University, Jinan, P.R. China, Jinan, China and Co-Innovation Center of Green Building, Jinan, China)
Tianyi Jiang (School of Municipal and Environmental Engineering, Shandong Jianzhu University, Jinan, China)
Yanyan Zhu (School of Municipal and Environmental Engineering, Shandong Jianzhu University, Jinan, China)
Yuanyuan Shao (School of Municipal and Environmental Engineering, Shandong Jianzhu University, Jinan, China)
Cuizhen Sun (School of Municipal and Environmental Engineering, Shandong Jianzhu University, Jinan, China)
Junsen Wu (School of Municipal and Environmental Engineering, Shandong Jianzhu University, Jinan, China)

Pigment & Resin Technology

ISSN: 0369-9420

Article publication date: 1 May 2019

Issue publication date: 1 May 2019

192

Abstract

Purpose

Self-organization has been regarded as a tool for the synthesis of well-defined organic nanostructures. Heterocyclic annulated perylene diimides are the subjects of considerable current research studies. The purpose of this study is to reveal the photophysical property, electronic structure and solid-state packing of O-heterocyclic annulated perylene diimide.

Design/methodology/approach

Asymmetrically five-membered O-heterocyclic annulated perylene diimide (OAPDI) was synthesized. Structure and purity of OAPDI were confirmed by 1H NMR, 13C NMR, IR and mass spectral techniques. Photophysical properties of OAPDI were studied using UV–vis absorption and fluorescence in both solution (CHCl3) and solid state. Scanning electron microscopic and atomic force microscopy were used to characterize the surface morphology of OAPDI. Conducting properties of the OAPDI were evaluated by current–voltage measurements. The compounds geometries were also optimized at 6-31G* using density functional theory.

Findings

The UV–vis absorption and fluorescence spectra of OAPDI in solution are blue-shifted in comparison with that of unsubstituted perylene bisimide. Solid-state UV–vis measurements of OAPDI indicate that it is capable of forming highly ordered structure. The non-covalent interactions, electrostatic attraction and p-p stacking moieties of OAPDI synergistically guide assembly and domain growth while maintaining the interpenetrating network of nanofibers in the solid film. The OAPDI gave higher current at −2.0 V (0.68 µA) and 4.0 V (1.0 µA).

Originality/value

This study will be helpful for exploring feasible routes to acquire soluble perylene diimides and well-defined organic nanostructures. Furthermore, such molecular tailoring approach would be helpful for designing and synthesizing novel organic semiconductive materials with excellent charge-transporting and light-emitting capabilities.

Keywords

Acknowledgements

The authors acknowledge Doctoral Foundation of Shandong Jianzhu University (Grant No. XNBS1712, XNBS1618 and XNBS1412), Science and Technology Plan Project of Housing and Urban-Rural Construction Department in Shandong Province (2018-K11-01), Science and Technology Plans of Ministry of Housing and Urban-Rural Development of the People’s Republic of China and Opening Projects of Beijing Advanced Innovation Center for Future Urban Design, Beijing University of Civil Engineering and Architecture (UDC2017031512), University Science and Technology Project of Shandong Province (J16LD05) and National Natural Science Foundation of China (51708338).

Conflict of interest: The authors declare no competing interests.

Citation

Li, W., Wang, Q., Ma, Y., Jiang, T., Zhu, Y., Shao, Y., Sun, C. and Wu, J. (2019), "Photophysical property, electronic structure and solid-state packing of O-heterocyclic annulated perylene diimide", Pigment & Resin Technology, Vol. 48 No. 3, pp. 256-262. https://doi.org/10.1108/PRT-04-2018-0034

Publisher

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Emerald Publishing Limited

Copyright © 2019, Emerald Publishing Limited

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