Naphthalocyanine

Naphthalocyanine
Names
	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
Identifiers
CAS Number	23627-89-6 ;
3D model (JSmol)	Interactive image;
ChemSpider	4677874 ;
PubChem CID	5748311;
CompTox Dashboard (EPA)	DTXSID50905112 ;
	InChI 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 ;
	SMILES C1(/N=C(C2=C/3C=C4C=CC=CC4=C2)\NC3=N/C(C5=C/6C=C(C=CC=C7)C7=C5)=NC6=N/8)=N/C(C9=CC%10=CC=CC=C%10C=C19)=N\C%11=C%12C=C%13C=CC=CC%13=CC%12=C8N%11;
Properties
Chemical formula	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).
	(what is ?)
	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.

Timmer, J. (2007) Storing data in molecules: shifting atoms and flipping bits, ars technica online [accessed 8 September 2007]

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