Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phthalonitrile | HCID 7042 | — |
| Katalysator | Titanium Tetrachloride | HCID 24193 | — |
| Lösungsmittel | 1-Chloronaphthalene | HCID 7003 | — |
| Produkt | Phthalocyanine | HCID 86280045 | — |
Reaktionsschritte
In this comparative example, α-titanyloxyphthalocyanine was prepared by the method disclosed in Japanese Patent Application Laying-open No.62-134651. That is, a mixture of 40 g of phthalodinitrile, 18 g of titanium tetrachloride, and 500 cc of chloronaphthalene was stirred at the temperature of 240° C. to 250° C. for 3 hours in nitrogenous atmosphere to completely react with each other. The mixture was filtrated after the reaction, and as a result dichlorothitanium phthalocyanine was obtained. The obtained dichlorothitanium was mixed with 300 cc of concentrated ammonium solution to obtain a mixture. Then the mixture was heat-refluxed for 1 hour and subjected to the purification by using a Soxhlet extractor. Consequently, titanyloxyphthalocyanine was obtained by drying the purified product. The resultant titanyloxyphthalocyanine was confirmed as α-type crystal having an X-ray diffraction spectrum which is the same as the one shown in FIG. 3.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05874570 |
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| Quelldatensatz | uspto-grants-1999_02 |
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| ORD ID | ord-22bf60cda7144d808e529c5e8e761ca4 |
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| Quellennotiz | uspto-grants-1999_02 |
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