Difference between revisions of "Phthalocyanine dye"

From CAMEO
Jump to navigation Jump to search
m (Text replace - "== Authority ==" to "== Sources Checked for Data in Record ==")
 
(One intermediate revision by one other user not shown)
Line 1: Line 1:
 
== Description ==
 
== Description ==
  
A chromophore composed of a conjugated system of double bonds that forms a color complex with a metal. Phthalocyanine type choromophores occur naturally in chlorophyll and animal blood. They were first synthesized in the 1920s and commercially introduced in the 1930s. Because they are insoluble, phthlocyanine dyes are also classified as pigments. Examples include [http://cameo.mfa.org/materials/fullrecord.asp?name=phthalocyanine%20green phthalocyanine green] and [http://cameo.mfa.org/materials/fullrecord.asp?name=phthalocyanine%20blue phthalocyanine blue]. The dyes are not chemically reactive and must be physically attached to the substrate with a binder or adhesive.
+
A chromophore composed of a conjugated system of double bonds that forms a color complex with a metal. Phthalocyanine type choromophores occur naturally in chlorophyll and animal blood. They were first synthesized in the 1920s and commercially introduced in the 1930s. Because they are insoluble, phthlocyanine dyes are also classified as pigments. Examples include [[phthalocyanine%20green|phthalocyanine green]] and [[phthalocyanine%20blue|phthalocyanine blue]]. The dyes are not chemically reactive and must be physically attached to the substrate with a binder or adhesive.
 
+
[[[SliderGallery rightalign|Phthalodyekes.jpg~Chemical structure]]]
 
== Synonyms and Related Terms ==
 
== Synonyms and Related Terms ==
  
 
phthalocyanine dyes; phthlocyanine pigments; aza[18]annulene dye; Monastral blue
 
phthalocyanine dyes; phthlocyanine pigments; aza[18]annulene dye; Monastral blue
  
[[[SliderGallery rightalign|Phthalodyekes.jpg~Chemical structure]]]
+
==Physical and Chemical Properties==
 
 
== Other Properties ==
 
  
 
Insoluble in water
 
Insoluble in water
  
== Sources Checked for Data in Record ==
+
==Resources and Citations==
 
 
* Website address 1  Comment: www.handprint.com
 
  
 +
* Website: www.handprint.com
 +
 
* Thomas B. Brill, ''Light Its Interaction with Art and Antiquities'', Plenum Press, New York City, 1980
 
* Thomas B. Brill, ''Light Its Interaction with Art and Antiquities'', Plenum Press, New York City, 1980
  
* Wikipedia, the free encyclopedia, at http://www.wikipedia.com  Comment: http://en.wikipedia.org/wiki/Phthalocyanine (Accessed Nov. 9, 2005)
+
* Wikipedia: http://en.wikipedia.org/wiki/Phthalocyanine (Accessed Nov. 9, 2005)
  
  
  
 
[[Category:Materials database]]
 
[[Category:Materials database]]

Latest revision as of 11:37, 4 August 2022

Description

A chromophore composed of a conjugated system of double bonds that forms a color complex with a metal. Phthalocyanine type choromophores occur naturally in chlorophyll and animal blood. They were first synthesized in the 1920s and commercially introduced in the 1930s. Because they are insoluble, phthlocyanine dyes are also classified as pigments. Examples include Phthalocyanine green and Phthalocyanine blue. The dyes are not chemically reactive and must be physically attached to the substrate with a binder or adhesive.

Chemical structure

Phthalodyekes.jpg

Synonyms and Related Terms

phthalocyanine dyes; phthlocyanine pigments; aza[18]annulene dye; Monastral blue

Physical and Chemical Properties

Insoluble in water

Resources and Citations

  • Website: www.handprint.com
  • Thomas B. Brill, Light Its Interaction with Art and Antiquities, Plenum Press, New York City, 1980

Retrieved from "https://cameo.mfa.org/index.php?title=Phthalocyanine_dye&oldid=90723"