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Structure

Tris(2,4-pentanedionato)iron(III)

CAS
14024-18-1
Catalog Number
ACM14024181-3
Category
Main Products
Molecular Weight
353.17
Molecular Formula
C15H21FeO6

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  • Product Description
  • Case Study
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Specification

Synonyms
FERRIC(III) ACETYLACETONATE;FERRIC ACETYLACETONATE;IRON (III) 2,4-PENTANEDIONATE;IRON(III) ACETYLACETONATE;IRON(III) ACETYLACETONE;IRON(+3)ACETYLACETONATE;IRON ACETYLACETONATE;ACETYLACETONE IRON(+3)
IUPAC Name
Iron(III) Acetylacetonate
Boiling Point
100ºC(9.7513 torr)
Melting Point
180-183ºC
Flash Point
43.1ºC
Appearance
orange crystalline powder
Application
Moderating and combustion catalyst, solid fuel catalyst, bonding agent, curing accelerator, intermediate.
Storage
Store below +30°C.
Exact Mass
356.09200
Hazard Statements
Xn:Harmful;
Safety Description
S26-S37/39
Stability
Stable. Incompatible with strong bases, strong oxidizing agents.

Tris(2,4-Pentanedionato)Iron(III) as a Precursor for the Synthesis of Iron Oxide Nanoparticles

Alothman, Asma A. Arabian Journal of Chemistry, 2024, 17(2), 105531.

The synthesis of iron oxide nanoparticles was achieved by pyrolysis of unirradiated and γ-irradiated tris(pentanedionato)iron(III) monomolecular precursors in static air. It was found that crystallites grew smaller and smaller as irradiation progressed, suggesting that radiation caused structural changes. These single-crystal iron oxide sizes, for unirradiated, γ-irradiated tris(2,4-pentanedionato)iron(III) at 100 and 300 kGy, were 18.23 0.23, 16.42 0.21 and 13.964 0.11 nm, respectively.
Synthesis of iron oxide nanoparticles from tris(pentanedionato)iron(III)
The irradiation procedure consisted of filling glass vials with tris(2,4-pentanedionato)iron(III) under vacuum and then irradiating with constant dose of about 26 kGy/h with a Co-60 Gamma cell 220. The total absorbed doses administered were 100 kGy and 300 kGy. To ensure proper calibration of the radiation source, a Fricke ferrous sulfate dosimeter was used for reference measurements. Dose calculations included adjustments to account for the photon mass attenuation and energy-absorption coefficients relevant to both the sample and the dosimeter solution. These adjustments were carefully implemented to guarantee the precision of the calculated doses. Tris(2,4-pentanedionato)iron(III) samples were subjected to calcination at temperatures of 180, 200, 220, 240, 260, and 280 °C for a duration of 6 hours each.

Tris(2,4-pentanedionato)iron(III) for Modification of QCM Chip with Artificial Siderophore-Fe3+ Complex

Inomata, Tomohiko, et al. Langmuir, 2012, 28(2), 1611-1617.

This work prepared three hydroxamic acid type artificial siderophores tris[2-3-(N-acyl-N-hydroxyamino)propylamidepropyl]aminomethane (1-3) terminally NH2 bonded and their Fe3+ complexes 4-6. Fe3+ complexes 4-6 were by reaction of compounds 1-3 with tris(2,4-pentanedionato)iron(III) as Fe3+ donor. Such synthetic siderophore complexes 4-6 could then be applied to modification of quartz crystal microbalance (QCM) chips to selectively absorb microbes.
Preparation of the Fe3+ Complexes 4-6
· Preparation of the Fe3+ Complex of 1 (4). The Fe(III) complexes of tris[2-{3-(N-acetyl-N-hydroxamino)propylamido}propyl]aminomethane (1) were synthesized following this procedure: a 20 mL aqueous solution of 1 (0.1 mmol) was mixed with a 20 mL ethyl acetate solution of tris(2,4-pentanedionato)iron(III) (0.1 mmol) and stirred vigorously at room temperature for 3 hours. The aqueous layer was then collected and completely evaporated, resulting in a quantitatively obtained deep-red oily solid.
· Preparation of the Fe3+ Complex of 2 (5). The complex 5 was synthesized using a similar method as described in the preparation of 4, substituting tris[2-{3-(N-propionyl-N-hydroxamino)propylamido}propyl]aminomethane (2) for 1, yielding an 88% product.
· Preparation of the Fe3+ Complex of 3 (6). Similarly, complex 6 was prepared following the same procedure as in 4, using tris[2-{3-(N-benzoyl-N-hydroxamino)propylamido}propyl]aminomethane in place of 1, with an 81% yield.

August 13, 2023


An accelerator
Tris(2,4-pentanedionato)iron(III) can effectively promote the curing of resin crosslinking agent, and the yield is improved.

What is the molecular formula of Tris(2,4-pentanedionato)iron(III)?

The molecular formula of Tris(2,4-pentanedionato)iron(III) is C15H21FeO6.

What is the molecular weight of Tris(2,4-pentanedionato)iron(III)?

The molecular weight of Tris(2,4-pentanedionato)iron(III) is 353.17 g/mol.

What are some synonyms for Tris(2,4-pentanedionato)iron(III)?

Some synonyms for Tris(2,4-pentanedionato)iron(III) are Iron(III) acetylacetonate, Ferric(III) acetylacetonate, and Acetylacetone Iron(III) Salt.

When was Tris(2,4-pentanedionato)iron(III) created?

Tris(2,4-pentanedionato)iron(III) was created on October 12, 2011.

What is the IUPAC name of Tris(2,4-pentanedionato)iron(III)?

The IUPAC name of Tris(2,4-pentanedionato)iron(III) is iron(3+);(E)-4-oxopent-2-en-2-olate.

What is the InChI of Tris(2,4-pentanedionato)iron(III)?

The InChI of Tris(2,4-pentanedionato)iron(III) is InChI=1S/3C5H8O2.Fe/c3*1-4(6)3-5(2)7;/h3*3,6H,1-2H3;/q;;;+3/p-3/b3*4-3+.

What is the CAS number of Tris(2,4-pentanedionato)iron(III)?

The CAS number of Tris(2,4-pentanedionato)iron(III) is 14024-18-1.

How many hydrogen bond acceptor counts does Tris(2,4-pentanedionato)iron(III) have?

Tris(2,4-pentanedionato)iron(III) has 6 hydrogen bond acceptor counts.

Is Tris(2,4-pentanedionato)iron(III) a canonicalized compound?

Yes, Tris(2,4-pentanedionato)iron(III) is a canonicalized compound.

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