Chromium(III) acetylacetonate

Chromium(III) acetylacetonate is the coordination compound with the formula Cr(C5H7O2)3, sometimes designated as Cr(acac)3. This purplish coordination complex is used in NMR spectroscopy as a relaxation agent because of its solubility in nonpolar organic solvents and its paramagnetism.

Chromium(III) acetylacetonate[1]
Solid Chromium (III) acetylacetonate
Solid chromium(III) acetylacetonate
Names
IUPAC name
Tris(acetylacetonato)chromium(III)
Other names
Tris(2,4-pentanediono)chromium(III), Cr(acac)3, Cr(pd)3
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.040.463
EC Number
  • 244-526-0
  • InChI=1S/3C5H7O2.Cr/c3*1-4(6)3-5(2)7;/h3*3H,1-2H3;/q3*-1;+3 checkY
    Key: GMJCSPGGZSWVKI-UHFFFAOYSA-N checkY
  • InChI=1/3C5H7O2.Cr/c3*1-4(6)3-5(2)7;/h3*3H,1-2H3;/q3*-1;+3
    Key: GMJCSPGGZSWVKI-UHFFFAOYAF
  • [Cr+3].O=C([CH-]C(=O)C)C.O=C([CH-]C(=O)C)C.O=C([CH-]C(=O)C)C
Properties
Cr(C5H7O2)3
Molar mass 349.32
Appearance deep maroon
Density 1.34 g/cm3
Melting point 210 °C (410 °F; 483 K)
Boiling point 340 °C (644 °F; 613 K) (sublimes near 110°C)[2]
Solubility in non-polar organic solvents soluble
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H315, H319, H335
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references

Synthesis and structure

The compound is prepared by the reaction of chromium(III) oxide with acetylacetone (Hacac):[3]

Cr2O3 + 6 Hacac → 2 Cr(acac)3 + 3 H2O

The complex has idealized D3 symmetry. The Cr-O distances are 1.93 Å.[4] The complex has been resolved into individual enantiomers by separation of its adduct with dibenzoyltartrate.[5]

Like many other Cr(III) compounds, it has a quartet ground state.

The complex is relatively inert toward substitution but undergoes bromination at the 3-positions of the chelate rings.

Use in NMR

Often paramagnetism in compounds is detrimental for NMR spectroscopy, as the spin-lattice relaxation times are very short which leads to excessively broad peaks. However, this can be put to advantage in the right circumstances.

The spin-lattice relaxation times for diamagnetic nuclei can be variable. In particular, 13C quaternary carbons suffer from low signal intensity due to long relaxation times and lack of enhancement from the Nuclear Overhauser effect. To circumvent the first issue, the addition of a small quantity (on the order of 0.1 mM) of Cr(acac)3 to an NMR sample reduces the relaxation time by providing an alternative relaxation pathway - namely through the unpaired electron.[6] By reducing the relaxation time, more scans can be acquired in a given amount of time, resulting in higher signal intensity. This is particularly advantageous for quantitative 13C NMR, which requires that all signals have fully relaxed between pulses. By reducing the relaxation time, the delay between pulses can be reduced without affecting the relative integrations of peaks.

See also

References
  1. Chromium acetylacetonate Archived 2015-04-16 at the Wayback Machine at American Elements
  2. Semyannikov, P.P.; Igumenov, I.K.; Trubin, S.V.; Chusova, T.P.; Semenova, Z.I. (February 2005). "Thermodynamics of chromium acetylacetonate sublimation". Thermochimica Acta. 432 (1): 91–98. doi:10.1016/j.tca.2005.02.034.
  3. Fernelius, W. Conard; Blanch, Julian E. (2007). "Chromium(III) Acetylacetonate". Inorganic Syntheses. Vol. 5. pp. 130–131. doi:10.1002/9780470132364.ch35. ISBN 9780470132364.
  4. Morosin, B. (1965). "The crystal structure of trisacetylacetonatochromium(III)". Acta Crystallographica. 19: 131–137. doi:10.1107/S0365110X65002876.
  5. Drake, A. F.; Gould, J. M.; Mason, S. F.; Rosini, C.; Woodley, F. J. (1983). "The optical resolution of tris(pentane-2,4-dionato)metal(III) complexes". Polyhedron. 2 (6): 537–538. doi:10.1016/S0277-5387(00)87108-9.
  6. Berger, Stefan; Braun, Siegmar (2004). 200 And More NMR Experiments: A Practical Course. Weinheim: Wiley-VCH. ISBN 3-527-31067-3.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.