Naphthalocyanine
Schematic and AFM image
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Names | |||
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Preferred IUPAC name
[11(2)Z,13(8)Z,33(4)Z,7(81)Z]-12H,52H-2,4,6,8-Tetraaza-1,3,5,7(1,3)-tetrakis(benzo[f]isoindola)cyclooctaphane-11(2),13(8),33(4),7(81)-tetraene | |||
Other names
Tetrabenzo[g]quinoxalino-2,3-porphyrazine
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Identifiers | |||
3D model (JSmol)
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PubChem CID
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CompTox Dashboard (EPA)
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Properties | |||
C48H26N8 | |||
Molar mass | 714.792 g·mol−1 | ||
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 | |||
Naphthalocyanine is a cross-shaped organic molecule consisting of 48 carbon, 8 nitrogen and 26 hydrogen atoms, it is a derivative of phthalocyanine. IBM Research labs used it for developing single-molecule logic switches[1] and visualizing charge distribution in a single molecule.[2][3]
Naphthalocyanine derivatives have a potential use in photodynamic cancer treatment.[4]
References[]
- ^ Liljeroth, P.; Repp, J.; Meyer, G. (2007). "Current-Induced Hydrogen Tautomerization and Conductance Switching of Naphthalocyanine Molecules". Science. 317 (5842): 1203–1206. Bibcode:2007Sci...317.1203L. doi:10.1126/science.1144366. PMID 17761878.
- ^ Mohn, F.; Gross, L.; Moll, N.; Meyer, G. (2012). "Imaging the charge distribution within a single molecule". Nature Nanotechnology. 7 (4): 227–231. Bibcode:2012NatNa...7..227M. doi:10.1038/NNANO.2012.20. PMID 22367099.
- ^ "Scientists image the charge distribution within a single molecule for the first time". Physorg.com. 2012-02-27. Retrieved 2012-02-27.
- ^ Shopova, M.; Woehrle, D.; Mantareva, V.; Mueller, S. (1999). "Naphthalocyanine Complexes as Potential Photosensitizers for Photodynamic Therapy of Tumors". Journal of Biomedical Optics. 4 (3): 276–85. doi:10.1117/1.429930. PMID 23015248.
External links[]
- Timmer, J. (2007) Storing data in molecules: shifting atoms and flipping bits, ars technica online [accessed 8 September 2007]
Categories:
- Phthalocyanines
- Molecular electronics
- Heterocyclic compound stubs