Fun Route: New Discovery of 63295-48-7

Different reactions of this compound(Iron(III) trifluoromethanesulfonate)Electric Literature of C3F9FeO9S3 require different conditions, so the reaction conditions are very important.

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: Iron(III) trifluoromethanesulfonate, is researched, Molecular C3F9FeO9S3, CAS is 63295-48-7, about A Nonheme Mononuclear {FeNO}7 Complex that Produces N2O in the Absence of an Exogenous Reductant.Electric Literature of C3F9FeO9S3.

A new nonheme iron(II) complex, FeII(Me3TACN)((OSiPh2)2O) (1), is reported. Reaction of 1 with NO(g) gives a stable mononitrosyl complex Fe(NO)(Me3TACN)((OSiPh2)2O) (2), which was characterized by Mossbauer (δ=0.52 mm s-1, |ΔEq|=0.80 mm s-1), EPR (S = 3/2), resonance Raman (RR) and Fe K-edge x-ray absorption spectroscopies. 2 Is an {FeNO}7 complex with an S = 3/2 spin ground state. The RR spectrum (λexc=458 nm) of 2 combined with isotopic labeling (15N, 18O) reveals ν(N-O)=1680 cm-1, which is highly activated, and is a nearly identical match to that seen for the reactive mononitrosyl intermediate in the nonheme iron enzyme FDPnor (ν(NO)=1681 cm-1). Complex 2 reacts rapidly with H2O in THF to produce the N-N coupled product N2O, providing the first example of a mononuclear nonheme iron complex that is capable of converting NO to N2O in the absence of an exogenous reductant.

Different reactions of this compound(Iron(III) trifluoromethanesulfonate)Electric Literature of C3F9FeO9S3 require different conditions, so the reaction conditions are very important.

Reference:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem