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Merck

546682

Copper(II) phthalocyanine

Dye content >99 %

Synonym(s):

CuPc, Phthalocyanine blue, Pigment Blue 15

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About This Item

Empirical Formula (Hill Notation):
C32H16CuN8
CAS Number:
147-14-8
Molecular Weight:
576.07
EC Number:
205-685-1
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
24878914
MDL number:
MFCD00010719
Colour Index Number:
74160
Beilstein/REAXYS Number:
4121848

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composition

Dye content, >99%

Quality Level

100

λmax

678 nm

OLED device performance

ITO/CuPc/NPD/Alq3/C60/Mg:Ag

  • Color: green
  • Max. Luminance: 17200 Cd/m2
, ITO/CuPc/NPD/Alq3/LiF/Al
  • Color: red
  • Max. Luminance: 2000 Cd/m2
  • Turn-On Voltage: 7.5 V
, ITO/CuPc/NPD/CBP:FIrpic (6%)/BAlq3/LiF/Al
  • Color: blue
  • Max. EQE: 4.5 %

OPV device performance

ITO/CuPc/PTCDA/In

  • Short-circuit current density (Jsc): 53.1 mA/cm2
  • Open-circuit voltage (Voc): 0.57 V
  • Fill Factor (FF): 0.61
  • Power Conversion Efficiency (PCE): 4.2 %
, ITO/PEDOT:PSS/CuPc/C60/BCP/Al
  • Short-circuit current density (Jsc): 18.8 mA/cm2
  • Open-circuit voltage (Voc): 0.58 V
  • Fill Factor (FF): 0.52
  • Power Conversion Efficiency (PCE): 3.6 %

SMILES string

c1ccc2c(c1)C3=NC4=[N@@H]5C(=Nc6n7c(N=C8c9ccccc9C%10=[N@@H]8[Cu]57N3C2=N%10)c%11ccccc6%11)c%12ccccc4%12

InChI

1S/C32H16N8.Cu/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

XCJYREBRNVKWGJ-UHFFFAOYSA-N

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Application


  • A facile molecularly engineered copper (II) phthalocyanine as hole transport material for planar perovskite solar cells with enhanced performance and stability: This study introduces a modified copper(II) phthalocyanine that enhances the performance and stability of perovskite solar cells (Yang et al., 2017).

  • Dopant-free methoxy substituted copper (II) phthalocyanine for highly efficient and stable perovskite solar cells: Discusses the synthesis and application of a methoxy-substituted copper(II) phthalocyanine, improving the efficiency and stability of perovskite solar cells (Ding et al., 2020).

  • Highly efficient dye-sensitized solar cells based on metal-free and copper (II) phthalocyanine bearing 2-phenylphenoxy moiety: Examines novel phthalocyanines for use in dye-sensitized solar cells, focusing on their synthesis and photophysical properties (Ali et al., 2016).

  • Operando HERFD-XANES and surface sensitive Delta mu analyses identify the structural evolution of copper (II) phthalocyanine for electroreduction of CO2: This research uses advanced spectroscopic techniques to explore the structural changes in copper(II) phthalocyanine during CO2 electroreduction (Mei et al., 2022).

  • New dye sensitized photocatalysts: Copper (II)-phthalocyanine/TiO2 nanocomposite for water remediation: Studies a copper(II) phthalocyanine-TiO2 composite as a photocatalyst for water remediation, showing its effectiveness in degrading pollutants under light irradiation (Albay et al., 2016).

Storage Class

11 - Combustible Solids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

546682-VAR: + 546682-BULK: + 546682-200MG:4548173944098 + 546682-2G:4548173944104

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Certificates of Analysis (COA)

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Yu Li Huang et al.
Langmuir : the ACS journal of surfaces and colloids, 26(5), 3329-3334 (2010-02-24)
The self-assembly of the binary molecular system comprising copper(II) phthalocyanine (CuPc) and copper-hexadecafluoro-phthalocyanine (F(16)CuPc) on graphite has been investigated by in situ low-temperature scanning tunneling microscopy (LT-STM). The adsorption of this binary molecular system on graphite results in the formation
Medhat A Shaibat et al.
The journal of physical chemistry. B, 114(13), 4400-4406 (2010-03-17)
Cu(II)(phthalocyanine) (CuPc) is broadly utilized as an archetypal molecular semiconductor and is the most widely used blue printing pigment. CuPc crystallizes in six different forms; the chemical and physical properties are substantially modulated by its molecular packing among these polymorphs.
Masaya Hirade et al.
ACS applied materials & interfaces, 3(1), 80-83 (2011-01-05)
To enhance the performance of organic photovoltaic (OPV) cells, preparation of organic nanometer-sized pillar arrays is fascinating because a significantly large area of a donor/acceptor heterointerface having continuous conduction path to both anode and cathode electrodes can be realized. In
Jia Liu et al.
Journal of the American Chemical Society, 133(51), 21010-21015 (2011-11-24)
The bottom-up fabrication of surface hierarchical nanostructures is of great importance for the development of molecular nanostructures for chiral molecular recognition and enantioselective catalysis. Herein, we report the construction of a series of 2D chiral hierarchical structures by trinary molecular
A Mugarza et al.
Physical review letters, 105(11), 115702-115702 (2010-09-28)
We study the electronic mechanisms underlying the induction and propagation of chirality in achiral molecules deposited on surfaces. Combined scanning tunneling microscopy and ab initio electronic structure calculations of Cu-phthalocyanines adsorbed on Ag(100) reveal the formation of chiral molecular orbitals
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