Reaktion #1256728

ord-0e711136faba4d52934f5a4a778ce7f2

Reaktionsgleichung

[O-2].[Ti+4].c1ccc2c(c1)-c1nc3nc(nc4[n-]c(nc5[n-]c(nc-2n1)c1ccccc51)c1ccccc41)-c1ccccc1-3
TiOPc
O
water
[O-2].[Ti+4].c1ccc2c(c1)-c1nc3nc(nc4[n-]c(nc5[n-]c(nc-2n1)c1ccccc51)c1ccccc41)-c1ccccc1-3
TiOPc
c1ccc2c(c1)-c1nc-2nc2[nH]c(nc3nc(nc4[nH]c(n1)c1ccccc41)-c1ccccc1-3)c1ccccc21
phthalocyanine
[O-2].[Ti+4].c1ccc2c(c1)-c1nc3nc(nc4[n-]c(nc5[n-]c(nc-2n1)c1ccccc51)c1ccccc41)-c1ccccc1-3
TiOPc

Lösungsmittel

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeSpecifically, the procedure for preparation of the wet cake
  2. 2
    Sonstigein Pigment Synthesis Example 1
  3. 3
    SonstigeThe wet cake was dried
  4. 4
    Sonstigeto prepare the TiOPc pigment
  5. 5
    WaschenThen the resultant TiOPc crystal was washed with methanol
  6. 6
    Waschenby washing with ion-exchange water
  7. 7
    Sonstigedrying

Vorschrift

A titanyl phthalocyanine crystal was prepared using the method described in Example 1 of JP-A 03-269064. Specifically, the procedure for preparation of the wet cake in Pigment Synthesis Example 1 was repeated. The wet cake was dried to prepare the TiOPc pigment. One gram of the TiOPc pigment was mixed with a mixture solvent of 10 g of ion-exchange water and 1 g of monochlorobenzene, and the mixture was agitated for 1 hour at 50° C. Then the resultant TiOPc crystal was washed with methanol, followed by washing with ion-exchange water and drying. Thus a TiOPc crystal 4 was prepared. No halogen-containing raw material was used for synthesizing the TiOPc crystal 4.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07824830B2uspto-grants-2010_11