Chemistry:Diindenoperylene
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| Names | |
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| Preferred IUPAC name
Diindeno[1,2,3-cd:1′,2′,3′-lm]perylene | |
| Other names
Periflanthen; Periflanthene
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| Identifiers | |
3D model (JSmol)
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| Abbreviations | DIP |
| ChemSpider | |
PubChem CID
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| Properties | |
| C32H16 | |
| Molar mass | 400.480 g·mol−1 |
| Appearance | Orange solid |
| Boiling point | >330 °C (sublimation) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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| Infobox references | |
Diindenoperylene (DIP) is an organic semiconductor which receives attention because of its potential application in optoelectronics (solar cells, OLEDs) and electronics (RFID tags). DIP is a planar perylene derivative with two indeno-groups attached to opposite sides of the perylene core. Its chemical formula is C32H16, the full chemical name is diindeno[1,2,3-cd:1',2',3'-lm]perylene. Its chemical synthesis has been described.[1][2]
Properties and uses
The molecular weight is 400.48 g/mol, the dimensions of the molecule in its plane are ~18.4×7 Å.[3] and its sublimation temperature is above 330 °C.[4] It is non-polar and therefore only slightly soluble, for example in acetone.
DIP is a red dye[5] and has been used as active material for optical recording.[6] Because of its ‘perylene-type’ optical emission in the visible spectrum, it has also been used in organic light emitting diodes.[7] Organic field effect transistors of DIP have been studied.[8] The charge carrier mobility achieved was up to 0.1 cm2/(V·s) for thin film transistors with silicon dioxide as gate dielectric, making DIP a good candidate for further optimisation.[9]
The structure of bulk DIP crystals has recently been studied by Pflaum et al., who found two distinct phases at room temperature and at temperatures above 160 °C. In thin films for growth ‘near equilibrium’ (at substrate temperature of about 130 °C) by organic molecular beam deposition (OMBD), DIP has been shown to order very well.[2][10] The structure of thin DIP films has been characterized ‘post-growth’,[2][11][12][13] with structures differing from the room-temperature bulk structure. These thin-film structures depend on the substrate used, and also on the substrate temperature during growth.[10]
References
- ↑ J. von Braun, G. Manz, in Deutsches Reichspatentamt, Berlin. (Germany, 1934).
- ↑ 2.0 2.1 2.2 E. Clar, Polycyclic hydrocarbons (Academic Press, London, New York, 1964), p. 2
- ↑ Dürr, A. C.; Schreiber, F.; Münch, M.; Karl, N.; Krause, B.; Kruppa, V.; Dosch, H. (2002). "High structural order in thin films of the organic semiconductor diindenoperylene". Applied Physics Letters 81 (12): 2276. doi:10.1063/1.1508436. Bibcode: 2002ApPhL..81.2276D.
- ↑ A. C. Dürr, Ph.D. thesis, Universität Stuttgart (2002)
- ↑ Heilig, M; Domhan, M; Port, H (2004). "Optical properties and morphology of thin diindenoperylene films". Journal of Luminescence 110 (4): 290. doi:10.1016/j.jlumin.2004.08.023. Bibcode: 2004JLum..110..290H.
- ↑ H. E. Simmons. (1987)
- ↑ H. Antoniadis, A. J. Bard. (Hewlett-Packard Company & The Board of Regents of The University of Palo Alto, CA, 1997)
- ↑ M. Münch, Ph.D. thesis, Universität Stuttgart (2001)
- ↑ N. Karl, in Organic Electronic Materials R. Farchioni, G. Grosso, Eds. (Springer, Berlin, 2001), vol. II, ISBN:3-540-66721-0 pp. 283 ff.
- ↑ 10.0 10.1 Kowarik, S.; Gerlach, A.; Sellner, S.; Schreiber, F.; Cavalcanti, L.; Konovalov, O. (2006). "Real-Time Observation of Structural and Orientational Transitions during Growth of Organic Thin Films". Physical Review Letters 96 (12): 125504. doi:10.1103/PhysRevLett.96.125504. PMID 16605925. Bibcode: 2006PhRvL..96l5504K.
- ↑ Dürr, A.; Schreiber, F.; Ritley, K.; Kruppa, V.; Krug, J.; Dosch, H.; Struth, B. (2003). "Rapid Roughening in Thin Film Growth of an Organic Semiconductor (Diindenoperylene)". Physical Review Letters 90 (1): 016104. doi:10.1103/PhysRevLett.90.016104. PMID 12570630. Bibcode: 2003PhRvL..90a6104D.
- ↑ Dürr, A.; Koch, N.; Kelsch, M.; Rühm, A.; Ghijsen, J.; Johnson, R.; Pireaux, J.-J.; Schwartz, J. et al. (2003). "Interplay between morphology, structure, and electronic properties at diindenoperylene-gold interfaces". Physical Review B 68 (11): 115428. doi:10.1103/PhysRevB.68.115428. Bibcode: 2003PhRvB..68k5428D. http://bib-pubdb1.desy.de/search?p=id:%22PUBDB-2017-11185%22.
- ↑ Hoshino, A; Isoda, Seiji; Kobayashi, Takashi (1991). "Epitaxial growth of organic crystals on organic substrates — polynuclear aromatic hydrocarbons". Journal of Crystal Growth 115 (1–4): 826–830. doi:10.1016/0022-0248(91)90854-X. Bibcode: 1991JCrGr.115..826H.
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