- Naphthalocyanine
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Naphthalocyanine 
(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)Identifiers PubChem 5748311 ChemSpider 4677874 
Jmol-3D images Image 1 - n1c%12nc(nc9nc(nc6nc(nc4nc1c3cc2ccccc2cc34)c5cc7c(cc56)cccc7)c%10cc8ccccc8cc9%10)c%13cc%11ccccc%11cc%12%13
- InChI=1S/C48H26N8/c1-2-10-26-18-34-33(17-25(26)9-1)41-49-42(34)54-44-37-21-29-13-5-6-14-30(29)22-38(37)46(51-44)56-48-40-24-32-16-8-7-15-31(32)23-39(40)47(52-48)55-45-36-20-28-12-4-3-11-27(28)19-35(36)43(50-45)53-41/h1-24H,(H2,49,50,51,52,53,54,55,56)
Key: LKKPNUDVOYAOBB-UHFFFAOYSA-N
Properties Molecular formula C48H26N8 Molar mass 714.774 
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Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)Infobox references Naphthalocyanine is a derivative of phthalocyanine used as a component in the development of IBM's single-molecule logic switch.
References
- Liljeroth, P., Repp, J. and Meyer, G. (2007) "Current-Induced Hydrogen Tautomerization and Conductance Switching of Naphthalocyanine Molecules", Science, 317 (5842: 31 August), p. 1203–1206, DOI: 10.1126/science.1144366
- Timmer, J. (2007) Storing data in molecules: shifting atoms and flipping bits, ars technica online [accessed 8 September 2007]
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