Lanthanide–tetrapyrrole complexes: synthesis, redox chemistry, photophysical properties, and photonic applications

Keyphrases

• Aptamer 50%
• Bioapplications 50%
• Bioimaging 50%
• Biological Windows 50%
• Biosensing 50%
• Chromism 100%
• Complex Synthesis 100%
• Conjugation 50%
• Derivatization 50%
• Edifices 50%
• Efficient Route 50%
• Fast Pathway 50%
• Highly Stable 50%
• Lanthanide Ions 50%
• Lanthanides 50%
• Light Emission 50%
• Luminescence 50%
• Macrocycles 50%
• Macrocyclic Compounds 50%
• Multinuclear 50%
• Naphthalocyanine 50%
• Near-infrared 50%
• Near-infrared Emission 100%
• Near-infrared Range 50%
• Near-infrared-II 50%
• Nonlinear Optical 50%
• Nonlinear Optical Properties 50%
• Paramagnetism 50%
• Photodynamic Therapy 50%
• Photonic Applications 100%
• Photophysical Properties 100%
• Phthalocyanine 50%
• Porpholactones 50%
• Porphyrin 50%
• Quantum Yield 50%
• Reaction Time 50%
• Redox Chemistry 100%
• Redox Properties 50%
• Redox State 50%
• Singlet Oxygen 50%
• Spectacular 50%
• Synthetic Organic Chemistry 50%
• Synthetic Protocols 50%
• Tetrapyrrole 100%
• Theranostics 50%
• Welcome 50%

Chemistry

• Chemistry 100%
• Derivatization 50%
• Lanthanoid Atom 100%
• Macrocycle 50%
• Macrocyclic Compound 50%
• Nonlinear Optical Property 50%
• Organic Chemistry 50%
• Paramagnetism 50%
• Photonics 100%
• Phthalocyanine 50%
• Porphyrin 50%
• Quantum Yield 50%
• Redox State 50%
• Sensitization 100%
• Tetrapyrrole 100%