Sources of common compounds: 2923-28-6

Here is just a brief introduction to this compound(2923-28-6)Reference of Silver(I) trifluoromethanesulfonate, more information about the compound(Silver(I) trifluoromethanesulfonate) is in the article, you can click the link below.

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: Silver(I) trifluoromethanesulfonate, is researched, Molecular CAgF3O3S, CAS is 2923-28-6, about Catalytic hydrogenation enabled by ligand-based storage of hydrogen.Reference of Silver(I) trifluoromethanesulfonate.

Biol. employs exquisite control over proton, electron, H-atom, or H2 transfer. Similar control in synthetic systems has the potential to facilitate efficient and selective catalysis. Here we report a dihydrazonopyrrole Ni complex where an H2 equivalent can be stored on the ligand periphery without metal-based redox changes and can be leveraged for catalytic hydrogenations. Kinetic and computational anal. suggests ligand hydrogenation proceeds by H2 association followed by H-H scission. This complex is an unusual example where a synthetic system can mimic biol.′s ability to mediate H2 transfer via secondary coordination sphere-based processes.

Here is just a brief introduction to this compound(2923-28-6)Reference of Silver(I) trifluoromethanesulfonate, more information about the compound(Silver(I) trifluoromethanesulfonate) is in the article, you can click the link below.

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem