Vanadyl 2,11,20,29-tetra-tert-butyl-2,3-naphthalo, identified by its CAS number 105011-00-5, is a coordination compound featuring vanadium in its +4 oxidation state, typically characterized by its blue color due to the presence of vanadyl ions. This compound is notable for its bulky tert-butyl substituents, which enhance its solubility in organic solvents and contribute to its steric hindrance, influencing its reactivity and stability. The naphthalene moiety in its structure provides aromatic characteristics, which can affect its electronic properties and interactions with other molecules. Vanadyl complexes are often studied for their potential applications in catalysis, materials science, and biological systems, particularly in relation to insulin-mimetic activities. The presence of multiple tert-butyl groups can also impart unique properties, such as increased lipophilicity and altered binding affinities in biological contexts. Overall, this compound exemplifies the intersection of coordination chemistry and organic synthesis, showcasing the versatility of vanadium-based compounds in various fields of research.

vanadyl 2,11,20,29-tetra-tert-butyl-2,3-naphthalo

105011-00-5: Vanadyl 2,11,20,29-tetra-tert-butyl-2,3-naphthalo, identified by its CAS number 105011-00-5, is a coordination compound featuring vanadium in its +4 oxidation state, typically characterized by its blue color due to the presence of vanadyl ions. This compound is notable for its bulky tert-butyl substituents, which enhance its solubility in organic solvents and contribute to its steric hindrance, influencing its reactivity and stability. The naphthalene moiety in its structure provides aromatic characteristics, which can affect its electronic properties and interactions with other molecules. Vanadyl complexes are often studied for their potential applications in catalysis, materials science, and biological systems, particularly in relation to insulin-mimetic activities. The presence of multiple tert-butyl groups can also impart unique properties, such as increased lipophilicity and altered binding affinities in biological contexts. Overall, this compound exemplifies the intersection of coordination chemistry and organic synthesis, showcasing the versatility of vanadium-based compounds in various fields of research.

Vanadyl 2,11,20,29-tetra-tert-butyl-2,3-naphthalocyanine is a molecule that has been synthesized by rationalizing the photostability of the vanadyl form. This molecule has ultrafast fluorescence due to its high quantum yield and is capable of being photoinduced by laser ablation. Vanadyl 2,11,20,29-tetra-tert-butyl-2,3-naphthalocyanine is also able to absorb a variety of wavelengths in the optical spectrum due to its conjugated double bonds. The molecule can be used as an optical material for use in semiconductor devices and heterojunction solar cells.

CAS 105011-00-5

vanadyl 2,11,20,29-tetra-tert-butyl-2,3-naphthalo

Vanadyl 2,11,20,29-tetra-tert-butyl-2,3-naphthalocyanine

Ref: 3D-FV168263