Naphthalocyanine

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Naphthalocyanine
Naphthalocyanine.svg
Names
IUPAC name
(2Z,15Z,27Z,41Z)-2,15,28,41,53,54,55,56-octaazatridecacyclo[40.10.1.13,14.116,27.129,40.04,13.06,11.017,26.019,24.030,39.032,37.043,52.045,50]hexapentaconta-1(53),2,4,6,8,10,12,14(56),15,17,19,21,23,25,27,29,31,33,35,37,39,41,43,45,47,49,51-heptacosaene (non-preferred name)
Other names
Tetrabenzo[g]quinoxalino-2,3-porphyrazine
Identifiers
23627-89-6 YesY
ChemSpider 4677874 YesY
Jmol-3D images Image
PubChem 5748311
Properties
C48H26N8
Molar mass 714.77 g·mol−1
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 YesY verify (what isYesY/N?)
Infobox references

Naphthalocyanine is a derivative of phthalocyanine used as a component in the development of IBM's single-molecule logic switch.[1]

It was used to show the first images of charge distribution over a single molecule in November 2011.[2][3]

Its derivatives may also have uses in photodynamic cancer treatment.[4]

References[edit]

  1. ^ Liljeroth, P.; Repp, J.; Meyer, G. (2007). "Current-Induced Hydrogen Tautomerization and Conductance Switching of Naphthalocyanine Molecules". Science 317 (5842): 1203–1206. doi:10.1126/science.1144366. PMID 17761878.  edit
  2. ^ Mohn, F.; Gross, L.; Moll, N.; Meyer, G. (2012). "Imaging the charge distribution within a single molecule". Nature Nanotechnology. doi:10.1038/NNANO.2012.20.  edit
  3. ^ "Scientists image the charge distribution within a single molecule for the first time". Physorg.com. 2012-02-27. Retrieved 2012-02-27. 
  4. ^ 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. doi:10.1117/1.429930.  edit

External links[edit]