Tetranaphtho[2,3-b:2',3'-g:2'',3''-l:2''',3'''-q]porphyrazine: Advanced Macrocycle for Photovoltaics, Electronics, and Biomedical Applications
Explore the cutting-edge applications of this advanced macrocyclic compound in technology and medicine.
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Tetranaphtho[2,3-b:2',3'-g:2'',3''-l:2''',3'''-q]porphyrazine
This highly conjugated macrocyclic compound, known by its CAS number 23627-89-6, possesses a unique planar architecture and an extensive π-electron delocalization. These structural features endow it with exceptional photophysical and electrochemical properties, making it a valuable component in the development of advanced materials.
- The unique electronic configuration of this porphyrazine derivative allows for efficient charge separation and transfer, which are crucial for enhancing the performance of photovoltaic devices, a key aspect of exploring naphthalocyanine in organic electronics.
- Its strong absorption in the visible to near-infrared region makes it suitable for applications in organic electronics, photodynamic therapy, and nonlinear optics, highlighting its role as a porphyrazine for photodynamic therapy.
- The compound's stability and tunable electronic properties further enhance its utility in advanced materials research, contributing to the study of advanced macrocyclic compounds for materials science.
- Its extended aromatic framework enhances its ability to absorb light across a broad spectrum, making it a promising candidate for applications in solar energy conversion, aligning with the use of tetrapyrrole derivatives in solar energy.
Key Advantages
Enhanced Optical Properties
Leverage the strong absorption across the visible to near-infrared spectrum for applications in advanced imaging, a significant benefit of near-infrared absorbing dyes for imaging.
Superior Electronic Performance
Benefit from efficient charge separation and transfer, critical for high-performance organic electronic devices, showcasing the power of stable conjugated macrocycles synthesis.
Therapeutic Potential
Explore its use as a photosensitizer in photodynamic therapy, offering novel treatment options in the biomedical field.
Key Applications
Organic Electronics
Utilize its excellent charge transport properties and broad light absorption in the development of organic field-effect transistors (OFETs) and organic light-emitting diodes (OLEDs).
Photovoltaic Devices
Its efficient charge separation and transfer capabilities make it a strong candidate for enhancing the performance of solar cells.
Photodynamic Therapy (PDT)
The compound's ability to generate singlet oxygen upon light irradiation makes it a promising photosensitizer for targeted cancer therapies.
Advanced Materials
Its unique structural and electronic properties are being explored for various applications in materials science, including as ligands in coordination chemistry.