Analyzing the synthesis route 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.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: Iron(III) trifluoromethanesulfonate, is researched, Molecular C3F9FeO9S3, CAS is 63295-48-7, about Crystal structure of bis{(3,5-dimethylpyrazol-1-yl)dihydro[3-(pyridin-2-yl)pyrazol-1-yl]borato}iron(II), the main research direction is crystal structure bisdimethylpyrazolyl dihydropyridinyl pyrazolyl boratoiron; FeII; crystal structure; discrete complex.; di­hydro­(pyrazole)(pyridlypyrazole)­borate derivative.Electric Literature of C3F9FeO9S3.

The structure determination of [Fe(C13H15BN5)2] was undertaken as part of a project on the modification of the recently published spin-crossover (SCO) complex [Fe{H2B(pz)(pypz)}2] (pz = pyrazole, pypz = pyridylpyrazole). To this end, a new ligand was synthesized in which two addnl. Me groups are present. Its reaction with iron trifluoromethanesulfonate led to a pure sample of the title compound, as proven by X-ray powder diffraction. The asym. unit consists of one complex mol. in a general position. The FeII atom is coordinated by two tridentate N-binding {H2B(3,5-(CH3)2-pz)(pypz)}- ligands. The Fe-N bond lengths range between 2.1222 (13) and 2.3255 (15) Å, compatible with FeII in the high-spin state, which was also confirmed by magnetic measurements. Other than a very weak C-H···N non-classical hydrogen bond linking individual mols. into rows extending parallel to [010], there are no remarkable intermol. interactions.

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