Crystal structure and optoelectronic properties of antiaromatic compound 3,4,9,10-tetrahydrodicyclopenta[cd,lm]perylene
Journal Article
·
· Crystallography Reports
- Nanjing University of Information Science and Technology, School of Environmental Science and Engineering (China)
An antiaromatic compound 3,4,9,10-tetrahydrodicyclopenta[cd,lm] perylene, was synthesized by a coupling reaction. Its crystal structure was determined by X-ray diffraction. Crystal structures shows that the antiaromatic compounds are aggregated to J-aggregation materials. It further results ultrafast charge separation at organic interface and electron transfer in the aggregation materials. UV-vis spectrum shows that title compound has a broad UV-vis light absorbance at the wavelength range from 250 to 470 nm and a 2.67 eV energy gap value between the highest occupied and the lowest unoccupied molecular orbital energy levels.
- OSTI ID:
- 22758326
- Journal Information:
- Crystallography Reports, Vol. 62, Issue 6; Other Information: Copyright (c) 2017 Pleiades Publishing, Inc.; Country of input: International Atomic Energy Agency (IAEA); ISSN 1063-7745
- Country of Publication:
- United States
- Language:
- English
Similar Records
Interaction of alkali metals with perylene-3,4,9,10- tetracarboxylic-dianhydride thin films
Vibrational characterization of Langmuir-Blodgett monolayers and evaporated films of a bisphenylene-substituted perylene-3,4,9,10-tetracarboxylic acid derivative
Ring-strain-modified properties of substituted perylene radical-cation salts. A solid-state sup 13 C CPMAS NMR study
Journal Article
·
Fri Jul 01 00:00:00 EDT 2005
· Journal of Applied Physics
·
OSTI ID:22758326
+2 more
Vibrational characterization of Langmuir-Blodgett monolayers and evaporated films of a bisphenylene-substituted perylene-3,4,9,10-tetracarboxylic acid derivative
Journal Article
·
Fri Jun 01 00:00:00 EDT 1990
· Langmuir; (USA)
·
OSTI ID:22758326
+1 more
Ring-strain-modified properties of substituted perylene radical-cation salts. A solid-state sup 13 C CPMAS NMR study
Journal Article
·
Wed Nov 07 00:00:00 EST 1990
· Journal of the American Chemical Society; (United States)
·
OSTI ID:22758326
+5 more