View text source at Wikipedia

Lead(II) phthalocyanine

Lead(II) phthalocyanine
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.156.674 Edit this at Wikidata
  • InChI=1S/C32H16N8.Pb/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
    Key: WSQYJDCCFQPFJC-UHFFFAOYSA-N
  • C1=CC=C2C(=C1)C3=NC4=C5C=CC=CC5=C6N4[Pb]N7C(=NC2=N3)C8=CC=CC=C8C7=NC9=NC(=N6)C1=CC=CC=C19
Properties
C32H16N8Pb
Molar mass 719.7 g·mol−1
Related compounds
Other cations
 Copper phthalocyanine
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Lead(II) Phthalocyanine (PbPc), also known as phthalocyanine lead, is a salt consisting of a lead ion and Pc2−, the conjugate base of pythalocyanine. It is a organolead dye and bright purple powder.[1][2] It's also used as a near infared light absorber for photodetectors.[3] It has a unique structural feature which is called and resembles a "shuttle cock."[3]

References

[edit]
  1. ^ Elements, American. "Lead(II) Phthalocyanine". American Elements. Retrieved 2024-05-24.
  2. ^ PubChem. "Phthalocyanine Lead". pubchem.ncbi.nlm.nih.gov. Retrieved 2024-05-24.
  3. ^ a b Kato, Masahiro; Yoshizawa, Hayato; Nakaya, Masato; Kitagawa, Yasutaka; Okamoto, Koichi; Yamada, Tomoaki; Yoshino, Masahito; Tanaka, Kentaro; Onoe, Jun (2022-05-25). "Unraveling the reasons behind lead phthalocyanine acting as a good absorber for near-infrared sensitive devices". Scientific Reports. 12 (1): 8810. Bibcode:2022NatSR..12.8810K. doi:10.1038/s41598-022-12990-z. ISSN 2045-2322. PMC 9132886. PMID 35614199.


Stub icon

This article about an organic compound is a stub. You can help Wikipedia by expanding it.