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About This Item
Empirical Formula (Hill Notation):
C32H16CoN8
CAS Number:
Molecular Weight:
571.46
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
222-012-7
Beilstein/REAXYS Number:
4121847
MDL number:
InChI key
MPMSMUBQXQALQI-UHFFFAOYSA-N
InChI
1S/C32H16N8.Co/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
SMILES string
[Co]1n2c3nc4nc(nc5n1c(nc6nc(nc2c7ccccc37)c8ccccc68)c9ccccc59)c%10ccccc4%10
form
powder
composition
Dye content, 97%
Quality Level
Related Categories
General description
Cobalt(II) phthalocyanine (CoPC )is a metallopthalocyanine.
Application
Self assembled molecules of CoPC were deposited on epitaxial graphene. CoPC may be used to develop carbon black based electrocatalysts. CoPC modified carbon paste may be used as indicators for electrocatalytic amperometric measurements. ZnO impregnated with CoPC may be used as a sensitizer to determine the photodegradation of cyanide in aqueous suspension. CoPC catalysed aerobic regenerations of aldehydes and ketones have been investigated. CoPC may also be used as an end capping agent of a hyperbranched poly(aryl ether ketone) to be used for oxidative decomposition of 2,4,6,-trichlorophenol.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Carc. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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R M Pemberton et al.
Biosensors & bioelectronics, 42, 668-677 (2012-12-26)
A water-based carbon screen-printing ink formulation, containing the redox mediator cobalt phthalocyanine (CoPC) and the enzyme glucose oxidase (GOx), was investigated for its suitability to fabricate glucose microbiosensors in a 96-well microplate format: (1) the biosensor ink was dip-coated onto
The use of copper and cobalt phthalocyanines as electrocatalysts for the oxygen reduction reaction in acid medium.
Reis RM, et al.
Electrochimica Acta, 139, 1-6 (2014)
Cobalt(II) phthalocyanine catalyzed aerobic regeneration of carbonyl compounds from the corresponding oximes in 1-butyl-3-methylimidazolium bromide
Shaabani A, et al.
Applied Catalysis A: General, 371(1-2), 148-152 (2009)
Tatsuhiko Honda et al.
Journal of the American Chemical Society, 134(9), 4196-4206 (2012-02-04)
Proton-coupled electron-transfer reduction of dioxygen (O(2)) to afford hydrogen peroxide (H(2)O(2)) was investigated by using ferrocene derivatives as reductants and saddle-distorted (α-octaphenylphthalocyaninato)cobalt(II) (Co(II)(Ph(8)Pc)) as a catalyst under acidic conditions. The selective two-electron reduction of O(2) by dimethylferrocene (Me(2)Fc) and decamethylferrocene
Preparation and characterization of a novel hyperbranched poly(aryl ether ketone) terminated with cobalt phthalocyanine to be used for oxidative decomposition of 2,4,6-trichlorophenol
Lei L, et al.
Macromolecular Research, 18(4), 331-335 (2010)
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