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Usage

Uses

Used in Paint Industry:
(TETRACARBOXYPHTHALOCYANINATO)COPPER(II) is used as a pigment for its excellent lightfastness, thermal stability, and high tinting strength, making it ideal for creating vibrant and long-lasting colors in the paint industry.
Used in Ink Industry:
In the ink industry, (TETRACARBOXYPHTHALOCYANINATO)COPPER(II) serves as a pigment due to its distinctive blue-green color, which is highly valued for producing high-quality and durable inks for various printing applications.
Used in Plastics Industry:
(TETRACARBOXYPHTHALOCYANINATO)COPPER(II) is used as a pigment in the plastics industry to impart a vibrant blue-green color to plastic products while maintaining their durability and resistance to environmental factors.
Used in Textile Industry:
In the textile industry, (TETRACARBOXYPHTHALOCYANINATO)COPPER(II) is utilized as a pigment to provide a stable and long-lasting blue-green color to fabrics, ensuring that the color remains vibrant even after multiple washes and exposure to sunlight.
Used in Electronics Industry:
(TETRACARBOXYPHTHALOCYANINATO)COPPER(II) has potential applications in the electronics industry, where its unique properties can be harnessed for the development of advanced electronic components and devices.
Used in Catalysis:
(TETRACARBOXYPHTHALOCYANINATO)COPPER(II) also has potential uses in catalysis, where its chemical properties can be employed to facilitate various chemical reactions and processes.
Used in Solar Cells:
(TETRACARBOXYPHTHALOCYANINATO)COPPER(II) can be used as a photosensitizer in solar cells, where its ability to absorb light can be utilized to improve the efficiency of energy conversion.
Safety Precaution:
It is important to handle (TETRACARBOXYPHTHALOCYANINATO)COPPER(II) with care, as copper can be toxic if ingested or inhaled. Proper safety measures should be taken to minimize the risk of exposure during its production, use, and disposal.

Upstream product

• 60469-86-5 3,4-dicyano benzoic acid 
• 132613-06-0 copper phthalocyanine(CONH₂)4 

Relevant academic research and scientific papers

Improved Synthesis of Soluble Metal-Free/Metal Phthalocyanine Tetracarboxylic Acids and Their Application in the Catalytic Epoxidation of Cyclohexene

Soluble metal-free and metal (copper (II), iron (III), and cobalt (II)) phthalocyanine tetracarboxylic acids (5-8) were synthesized using a novel method consisting of improved hydrolysis based on the diazo reaction. The obtained compounds (5-8) were characterized by X-ray diffraction, UV-Vis spectrometry, and FT-IR spectrometry and then utilized as catalysts for the epoxidation of cyclohexene with molecular oxygen as oxidant. Reaction conditions including reaction time, temperature, catalyst amount, and isobutyraldehyde/cyclohexene ratio were optimized to achieve the highest selectivity of cyclohexene oxide. Metal-free phthalocyanine tetracarboxylic acid (5) and metal (copper (II), iron (III), and cobalt (II)) phthalocyanine tetracarboxylic acids (6-8, respectively) were compared. Complexes 6-8 exhibited higher catalytic activity than compound 5 under the optimal conditions. Graphical Abstract: Four soluble metal-free and metal PTCs were synthesized using a novel method, and were utilized as catalysts for the epoxidation of cyclohexene with molecular oxygen as the oxidant. A total of 58.1% selectivity and yield of cyclohexene oxide were achieved under the optimal condition. [Figure not available: see fulltext.]

Highly efficient, mild, bromide-free and acetic acid-free dioxygen oxidation of p-nitrotoluene to p-nitrobenzoic acid with metal phthalocyanine catalysts

Four metal tetracarboxyl phthalocyanines were synthesized and characterized by elemental analysis and mass spectrometry. p-Nitrobenzoic acid was efficiently prepared in high yield from bromide-free and acetic acid-free aerobic oxidation of p-nitrotoluene using metal phthalocyanines as catalysts under mild conditions in alkali-methanol solution. Up to 88.8% isolated yield of p-nitrobenzoic acid was obtained with the catalysis of tetracarboxyl phthalocyanine cobalt (0.13 mol %, based on the moles of p-nitrotoluene) optionally combined with a small amount of dimethylformamide in the presence of 2.0 MPa dioxygen at 30-60°C. The effect on catalytic performance of a carboxyl group introduced into the phthalocyanine ring was further discussed on the basis of metal coordination chemistry theory.