Catalog Number
ACM132161-2
Product Name
Iron(II) phthalocyanine
Category
Phthalonitriles & Naphthalonitriles; Electronic Materials; Molecular Conductors; Other Materials; Phthalocyanine Dyes, Porphyrin Dyes
Synonyms
Phthalocyanine Iron(II)
Description
Alfa Chemistry offers Iron(II) Phthalocyanine products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page.
Molecular Formula
C32H16FeN8
Canonical SMILES
C1=CC=C2C(=C1)C3=NC4=NC(=NC5=C6C=CC=CC6=C([N-]5)N=C7C8=CC=CC=C8C(=N7)N=C2[N-]3)C9=CC=CC=C94.[Fe+2]
InChI
InChI=1S/C32H16N8.Fe/c1-2-10-18-17(9-1)25-33-26(18)38-28-21-13-5-6-14-22(21)30(35-28)40-32-24-16-8-7-15-23(24)31(36-32)39-29-20-12-4-3-11-19(20)27(34-29)37-25;/h1-16H;/q-2;+2
InChI Key
MIINHRNQLVVCEW-UHFFFAOYSA-N
Appearance
Dark purple powder to crystal
Application
The phthalocyanato metal complexes are artificial dyes for painting of railway trains, and for organic photoconductors of electrophotography. There are applications of organic semiconductors as organic transistors and hole injection materials for organic light-emitting diodes (OLED).
Features And Benefits
The phthalocyanato metal complexes show a more intense Q band absorption than that of the Soret band. Their absorption wavelengths are shifted to longer wavelengths than those of porphyrin compounds. Absorption wavelength is further shifted to the near infrared area by modification of the central metal and expansion of the π-conjugates. Introduction of an alkyl group provides soluble phthalocyanine and porphyrin compounds, although they are poorly soluble due to the large π-conjugated cycle.
Hydrogen Bond Acceptor Count
8
Hydrogen Bond Donor Count
0
Monoisotopic Mass
568.084728
Storage Conditions
Store at room temperature and dry
Topological Polar Surface Area
79.3 Ų