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Bis(acetylacetonato)iron(II)

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Bis(acetylacetonato)iron(II)
Names
IUPAC name Bis(2,4-pentanedionato-κO,κO')iron
Other names Bis(2,4-pentanedionato)iron
Ferrous acetylacetonate
Iron(II) 2,4-pentanedionate
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.034.397 Edit this at Wikidata
EC Number
  • 237-851-4
PubChem CID
InChI
  • InChI=1S/2C5H8O2.Fe/c2*1-4(6)3-5(2)7;/h2*3,6H,1-2H3;/q;;+2/p-2/b2*4-3-;Key: LFORAFQNBQKDRY-FDGPNNRMSA-L
  • hydrate: InChI=1S/2C5H8O2.Fe.H2O/c2*1-4(6)3-5(2)7;;/h2*3,6H,1-2H3;;1H2/b4-3-;;;Key: XTPSXHDLJKIQTA-FGSKAQBVSA-N
SMILES
  • C/C(=C/C(=O)C)/.C/C(=C/C(=O)C)/.
  • hydrate: CC(=CC(=O)C)O.C/C(=C/C(=O)C)/O.O.
Properties
Chemical formula C10H14FeO4
Molar mass 254.063 g·mol
Melting point 170–171 °C (338–340 °F; 443–444 K)
Hazards
GHS labelling:
Pictograms GHS07: Exclamation mark
Signal word Warning
Hazard statements H315, H319, H335
Precautionary statements P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Bis(acetylacetonato)iron(II) is a coordination complex of iron with the formula Fe(C5H7O2)2. It can be prepared by reacting iron(II) chloride with 2,4-pentanedione in presence of piperidine.

Reactions

Bis(acetylacetonato)iron(II) reacts with lithium bis(hydropentalenyl)iron to afford green 2-, a quadruple-decker complex.

It reacts with Li2Pn(TMEDA)x (Pn = permethylpentalene) to yield purple-black Fe2Pn2.

References

  1. "Iron (II) acetylacetonate hydrate". pubchem.ncbi.nlm.nih.gov.
  2. Manríquez, J. M., Bunel, E. E., Oelckers, B., Román, E., Vv́squez, C., & Miller, J. S. (2007). Bis(2,4-Pentanedionato)Iron(II) . Inorganic Syntheses, 267–269. doi:10.1002/9780470132623.ch44
  3. Oelckers, B., Chavez, I., Manriquez, J. M., & Roman, E. (1993). On the way to delocalized organometallic polymers: triple- and quadruple-decker pentalene complexes of iron and cobalt. Organometallics, 12(9), 3396–3397. doi:10.1021/om00033a007
  4. Binding, S. C., Green, J. C., Myers, W. K., & O’Hare, D. (2015). Synthesis, Structure, and Bonding for Bis(permethylpentalene)diiron. Inorganic Chemistry, 54(24), 11935–11940. doi:10.1021/acs.inorgchem.5b02254
Iron compounds
Fe(−II)
Fe(0)
Fe(I)
Organoiron(I) compounds
  • (C5H5FeCO)2(CO)2
  • Fe(0,II)
    Fe(II)
    Organoiron(II) compounds
    Fe(0,III)
    Fe(II,III)
    Fe(III)
    Organoiron(III) compounds
    Fe(IV)
    Fe(VI)
    Purported
    sort
    Metal acetylacetonate complexes
    H(acac) He
    Li Be B C N O F Ne
    Na(acac) Mg Al(acac)3 Si P S Cl Ar
    K Ca Sc(acac)3 Ti(acac)2Cl2
    Ti(acac)3
    V(acac)3
    VO(acac)2
    Cr(acac)2
    Cr(acac)3
    Mn Fe(acac)2
    Fe(acac)3
    Co(acac)2
    Co(acac)3
    3 Cu(acac)2 Zn(acac)2 Ga(acac)3 Ge As Se Br Kr
    Rb Sr Y(acac)3 Zr(acac)4 Nb MoO2(acac)2 Tc Ru(acac)3 Rh(acac)(CO)2
    Rh(acac)3
    Pd(acac)2 Ag Cd In(acac)3 Sn Sb Te I Xe
    Cs Ba(acac)2 * Lu(acac)3 Hf(acac)4 Ta W Re Os Ir(acac)3 Pt(acac)2 Au Hg Tl(acac) Pb Bi Po At Rn
    Fr Ra ** Lr Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
     
    * La(acac)3 Ce(acac)3 Pr(acac)3 Nd(acac)3 Pm Sm(acac)3 Eu(fod)3
    Eu(acac)3
    Gd(acac)3 Tb(acac)3 Dy(acac)3 Ho(acac)3 Er(acac)3 Tm(acac)3 Yb(acac)3
    ** Ac Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No
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