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Sigma-Aldrich

Zinc phthalocyanine

Dye content 97 %

Synonyme(s) :

Phthalocyanine zinc salt

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About This Item

Formule empirique (notation de Hill):
C32H16N8Zn
Numéro CAS:
Poids moléculaire :
577.91
Numéro Beilstein :
4121852
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352103
ID de substance PubChem :

Composition

Dye content, 97%

Niveau de qualité

Pertinence de la réaction

reagent type: catalyst
core: zinc

λmax

701 nm

Énergie orbitale

HOMO 5.17 eV (CV)
LUMO 3.78 eV (CV)

Performance des dispositifs OPV

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 %

Chaîne SMILES 

[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

Clé InChI

PODBBOVVOGJETB-UHFFFAOYSA-N

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Description générale

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.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


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Consulter la Bibliothèque de documents

Ye-Liang Wang et al.
Chimia, 66(1-2), 31-37 (2012-05-02)
We report on high-resolution STM measurements with modified probe tips. First, both the rest atoms and adatoms of a Si(111)-7×7 surface are observed simultaneously. The visibility of rest atoms is dependent upon the sample bias voltage (less than -0.7 V)
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
Effect of blend layer morphology on performance of ZnPc:C60-based photovoltaic cells
Zeng, W.; et al.
Applied Physics Letters, 97, 133304-133304 (2010)
Thandekile P Mthethwa et al.
Dalton transactions (Cambridge, England : 2003), 42(14), 4922-4930 (2013-02-07)
A novel thiol functionalized zinc phthalocyanine complex (ZnPcSH) is reported in this work. This complex was conjugated to gold nanoparticles. The photophysical and photochemical properties of the complex and the conjugate were investigated. Upon conjugation a blue shift was observed
Sean Marrache et al.
Integrative biology : quantitative biosciences from nano to macro, 5(1), 215-223 (2012-07-27)
A therapeutic technology that combines the phototoxic and immune-stimulating ability of photodynamic therapy (PDT) with the widespread effectiveness of the immune system can be very promising to treat metastatic breast cancer. We speculated that the knowledge of molecular mechanisms of

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