Introduction of a new synthetic route about 1260795-42-3

There is still a lot of research devoted to this compound(SMILES：O=C(C1C(C=O)=CC(Br)=CC=1)OC)Electric Literature of C9H7BrO3, and with the development of science, more effects of this compound(1260795-42-3) can be discovered.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Covalent bonds immobilization of cofacial Mn porphyrin dimers on an ITO electrode for efficient water oxidation in aqueous solutions, published in 2017-08-31, which mentions a compound: 1260795-42-3, mainly applied to covalent bond immobilization cofacial manganese porphyrin dimer electrocatalyst; ITO electrode water oxidation catalytic oxygen evolution, Electric Literature of C9H7BrO3.

The authors previously reported several Mn porphyrin dimers as the 1st Mn-containing mol. catalysts for H2O oxidation, however, in nonaqueous MeCN solution containing 5% H2O. Here, the authors successfully fabricated these dimers with mono- and hexaphosphonic acid groups, Mn2DP-PO3H2 and Mn2DP-(PO3H2)6, to covalently assemble them on the surface of ITO electrode (ITO = In-doped Sn oxide) and use the Mn2DP-PO3H2 and Mn2DP-(PO3H2)6|ITO assemblies as heterogeneous catalysts for electrochem. H2O oxidation in aqueous buffer solutions The mono-phosphonic acid fabricated assemblies showed unprecedent high turnover frequencies (TOFs) (up to 44.9 s-1) at a low overpotential (η = 0.47 V) in a neutral buffer solution In acidic buffered solutions (pH = 1.5), they showed higher TOFs (up to 47.4 s-1) at a very low overpotential (η = 0.26 V). The robustness of the mono-phosphonic acid fabricated catalysts, Mn2DP-PO3H2|ITO, was tested at a high overpotential (η = 0.80 V). Although they showed an O evolution with 178.3 s-1 TOF, the O evolution completely stopped after 11 h electrolysis. UV-visible spectra monitored during the electrolysis clearly indicated the gradual detachment of the catalysts from the ITO surface is likely the main reason of stopping the O evolution. The hexa-phosphonic acid catalyst assembly, Mn2DP-(PO3H2)6|ITO, however, showed a continuous O evolution without stopping even after 23 h of electrolysis with 199.3 s-1 TOF. Tafel plots in different pHs give insights on the mechanism of H2O oxidation

There is still a lot of research devoted to this compound(SMILES：O=C(C1C(C=O)=CC(Br)=CC=1)OC)Electric Literature of C9H7BrO3, and with the development of science, more effects of this compound(1260795-42-3) can be discovered.

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem