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341169

Sigma-Aldrich

Zinc phthalocyanine

Dye content 97 %

Sinónimos:

Phthalocyanine zinc salt

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About This Item

Fórmula empírica (notación de Hill):
C32H16N8Zn
Número de CAS:
14320-04-8
Peso molecular:
577.91
Beilstein/REAXYS Number:
4121852
EC Number:
238-262-5
MDL number:
MFCD00041955
UNSPSC Code:
12352103
PubChem Substance ID:
24860701
NACRES:
NA.23

composition

Dye content, 97%

Quality Level

100

reaction suitability

reagent type: catalyst
core: zinc

λmax

701 nm

orbital energy

HOMO 5.17 eV (CV)
LUMO 3.78 eV (CV)

OPV device performance

ITO/ZnPc:P60 (1:1)/Bphen/Ag

  • Short-circuit current density (Jsc): 11.7 mA/cm2
  • Open-circuit voltage (Voc): 0.54 V
  • Fill Factor (FF): 0.62
  • Power Conversion Efficiency (PCE): 3.9 %

SMILES string

[Zn]1n2c3nc4nc(nc5n1c(nc6nc(nc2c7ccccc37)c8ccccc68)c9ccccc59)c%10ccccc4%10

InChI

1S/C32H16N8.Zn/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

PODBBOVVOGJETB-UHFFFAOYSA-N

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General description

Zinc (II) phthalocyanine (ZnPc) complexes show photosensitizing properties. Phthalocyanines show significant Π−Π interactions and easy formation of H aggregates.

Application

Zinc phthalocyanine finds general applications in industry (catalysts, photoconductors etc) and biomedical (photodynamic therapy, PDT). ZnPc may be used to photooxidise cyclohexane. A study reports functionalization of polymer membrane with ZnPc.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
0000267004
SHBQ3573
SHBP9359
MKCN2418
MKCH0531

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Characterization of ITO/CuPc/Al and ITO/ZnPc/Al structures using optical and capacitance spectroscopy
Reis, F. T.; et al.
Synthetic Metals, 138, 33-37 (2003)
Polyamide nanofiber membranes functionalized with zinc phthalocyanines.
Goethals A, et al.
Journal of Applied Polymer Science, 131(13) (2014)
I M Tynga et al.
Journal of photochemistry and photobiology. B, Biology, 120, 171-176 (2012-12-26)
The development of curative techniques which are selective for neoplasms is one of the main focal areas in cancer research. The mechanism of cell damage due to Zinc phthalocyanine (ZnPcSmix)-mediated photodynamic therapy (PDT) in a breast cancer cell line (MCF-7)
Anamika Ray et al.
The journal of physical chemistry. B, 116(39), 11979-11998 (2012-08-23)
The present article reports photophysical studies on supramolecular interaction of a zinc phthalocyanine derivative, namely, zinc-2,9,16,23-tetra-tert-butyl phthalocyanine (1) with C(60) and C(70) in solvents having varying polarity, i.e., toluene and 1,2-dichlorobenzene (DCB). The interesting feature of the present work is
Junseok Lee et al.
Chemical communications (Cambridge, England), 49(15), 1545-1547 (2013-01-18)
A photoresponsive drug releasing system based on mesoporous silica nanoparticles (MSN) was developed. A model drug was decorated on the surfaces via singlet oxygen sensitive linkers and a singlet oxygen-generating photosensitizer was loaded in the mesopores of the MSN. An
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