Brief introduction of C10H16CuO4

If you are interested in 13395-16-9, you can contact me at any time and look forward to more communication. Reference of 13395-16-9

Chemistry graduates have much scope to use their knowledge in a range of research sectors, including roles within chemical engineering, chemical and related industries, healthcare and more. Reference of 13395-16-9. Introducing a new discovery about 13395-16-9, Name is Bis(acetylacetone)copper, The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis.

The aerobic oxidation of substituted phenols with the catalytic system M(acac)n/3-methylbutanal/O2 has been investigated. Co(acac)2 and Mn(acac)3 promoted the transformation of 2,6-dimethylphenol and 2,6-di-t-butylphenol into their corresponding diphenoquinones and benzoquinones. In the oxidation of 2,3,6-trimethylphenol, the same catalysts yielded 32-34% of the relevant biphenol. Cu(acac)2 converted 2-naphthol into 1,1?-bi-2-naphthol with 84% yield. Supported Co(II) and Cu(II) complexes have also been used as heterogeneous catalysts for the oxidation of 2,6-di-t-butylphenol and 2-naphthol, respectively.

If you are interested in 13395-16-9, you can contact me at any time and look forward to more communication. Reference of 13395-16-9

Reference:
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”