Chemistry:Transition metal oxo complex

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Short description: Coordination complex containing an oxo ligand
a) Doubly bridging and b) terminal oxo ligands

A transition metal oxo complex is a coordination complex containing an oxo ligand. Formally O2-, an oxo ligand can be bound to one or more metal centers, i.e. it can exist as a terminal or (most commonly) as bridging ligands (Fig. 1). Oxo ligands stabilize high oxidation states of a metal.[1] They are also found in several metalloproteins, for example in molybdenum cofactors and in many iron-containing enzymes. One of the earliest synthetic compounds to incorporate an oxo ligand is potassium ferrate (K2FeO4), which was likely prepared by Georg E. Stahl in 1702.[2]

Reactivity

Olation and acid-base reactions

Sodium decavanadate, one of many polyoxometallate salts. The structure illustrates terminal oxo, doubly-bridging oxo, triply bridging oxo, and six-fold bridging oxo ligands.

A common reaction exhibited by metal-oxo compounds is olation, the condensation process that converts low molecular weight oxides to polymers with M-O-M linkages. Olation often begins with the deprotonation of a metal-hydroxo complex. It is the basis for mineralization and the precipitation of metal oxides. For the oxides of d0 metals, VV, NbV, TaV, MoVI, and WVI, the olation process affords polyoxometallates, a large class of molecular metal oxides.

Oxygen-atom transfer

Metal oxo complexes are intermediates in many metal-catalyzed oxidation reactions. Oxygen-atom transfer is common reaction of particular interest in organic chemistry and biochemistry.[3] Some metal-oxos are capable of transferring their oxo ligand to organic substrates. One such example of this type of reactivity is from and enzyme superfamily Molybdenum oxotransferase.

In water oxidation catalysis, metal oxo complexes are intermediates in the conversion of water to O2.

Hydrogen-atom abstraction

Transition metal-oxo's are also capable of abstracting strong C–H, N–H, and O–H bonds. Cytochrome P450 contains a high-valent iron-oxo which is capable of abstracting hydrogen atoms from strong C–H bonds.[4]

Molecular oxides

Some of the longest known and most widely used oxo compounds are oxidizing agents such as potassium permanganate (KMnO4) and osmium tetroxide (OsO4).[5] Compounds such as these are widely used for converting alkenes to vicinal diols and alcohols to ketones or carboxylic acids.[1] More selective or gentler oxidizing reagents include pyridinium chlorochromate (PCC) and pyridinium dichromate (PDC).[1] Metal oxo species are capable of catalytic, including asymmetric oxidations of various types. Some metal-oxo complexes promote C-H bond activation, converting hydrocarbons to alcohols.[6]

Selection of molecular metal oxides. From left, vanadyl chloride (d0), a tungsten oxo carbonyl (d2), permanganate (d0), [ReO2(pyridine)4]+ (d2), simplified view of compound I (a state of cytochrome P450, d4), and Ir(O)(mesityl)3 (d4).[7]

Metalloenzymes

Iron(IV)-oxo species

Oxygen rebound mechanism used by cytochrome P450 enzymes for oxidation of aliphatic groups to alcohols by the action of Compound I (adapted from [8]

Iron(IV)-oxo compounds are intermediates in many biological oxidations:

  • Alpha-ketoglutarate-dependent hydroxylases activate O2 by oxidative decarboxylation of ketoglutarate, generating Fe(IV)=O centers, i.e. ferryl, that hydroxylate a variety of hydrocarbon substrates.[9]
  • Cytochrome P450 enzymes, use a heme cofactor, insert ferryl oxygen into saturated C–H bonds,[10] epoxidize olefins,[11][12] and oxidize aromatic groups.[13]
  • Methane monooxygenase (MMO) oxidizes methane to methanol via oxygen atom transfer from an iron-oxo intermediate at its non-heme diiron center.[14] Much effort is aimed at reproducing reactions with synthetic catalysts.[6]

Molybdenum/tungsten oxo species

Three structural families of molybdenum cofactors: a) xanthine oxidase, b) sulfite oxidase, and c) (DMSO) reductase. The DMSO reductase features two molybdopterin ligands attached to molybdenum. They are omitted from the figure for simplicity. The rest of the heterocycle is similar to what is shown for the other two cofactors.

The oxo ligand (or analogous sulfido ligand) is nearly ubiquitous in molybdenum and tungsten chemistry, appearing in the ores containing these elements, throughout their synthetic chemistry, and also in their biological role (aside from nitrogenase). The biologically transported species and starting point for biosynthesis is generally accepted to be oxometallates MoO4−2 or WO4−2. All Mo/W enzymes, again except nitrogenase, are bound to one or more molybdopterin prosthetic group. The Mo/W centers generally cycle between hexavalent (M(VI)) and tetravalent (M(IV)) states. Although there is some variation among these enzymes, members from all three families involve oxygen atom transfer between the Mo/W center and the substrate.[15] Representative reactions from each of the three structural classes are:

The three different classes of molybdenum cofactors are shown in the Figure. The biological use of tungsten mirrors that of molybdenum.[16]

Oxygen-evolving complex

The active site for the oxygen-evolving complex (OEC) of photosystem II (PSII) is a Mn4O5Ca centre with several bridging oxo ligands that participate in the oxidation of water to molecular oxygen.[17] The OEC is proposed to utilize a terminal oxo intermediate as a part of the water oxidation reaction. This complex is responsible for the production of nearly all of earth's molecular oxygen. This key link in the oxygen cycle is necessary for much of the biodiversity present on earth.

X-ray Crystal structure of the Mn4O5Ca core of the oxygen evolving complex of Photosystem II at a resolution of 1.9 Å.[17]

The "oxo wall"

Qualitative molecular orbital diagram of a d0 metal-oxo fragment (empty metal d orbitals in an octahedral field on left, full oxygen p orbitals on right). Here it can be seen that d1-2 electrons fill a nonbonding orbital and electrons d3-6 fill anti-bonding orbitals, which destabilize the complex.[18]

The term "oxo wall" is a theory used to describe the fact that no terminal oxo complexes are known for metal centers with octahedral symmetry and d-electron counts beyond 5.[18][19]

Oxo compounds for the vanadium through iron triads (Groups 3-8) are well known, whereas terminal oxo compounds for metals in the cobalt through zinc triads (Groups 9-12) are rare and invariably feature metals with coordination numbers lower than 6. This trend holds for other metal-ligand multiple bonds. Claimed exceptions to this rule[20][21][22] have been retracted.[23][24][25]

The iridium oxo complex Ir(O)(mesityl)3 may appear to be an exception to the oxo-wall, but it is not because the complex is non-octahedral.[7] The trigonal symmetry reorders the metal d-orbitals below the degenerate MO π* pair. In three-fold symmetric complexes, multiple MO bonding is allowed for as many as 7 d-electrons.[18]

Terminal oxo ligands are also rather rare for the titanium triad, especially zirconium and hafnium and are unknown for group 3 metals (scandium, yttrium, and lanthanum).[1]

See also

References

  1. ↑ 1.0 1.1 1.2 1.3 Nugent, W. A., Mayer, J. M. "Metal-Ligand Multiple Bonds." John Wiley & Sons, New York, 1988.
  2. ↑ Delaude, Lionel; Laszlo, Pierre (1996-01-01). "A Novel Oxidizing Reagent Based on Potassium Ferrate(VI)1". The Journal of Organic Chemistry 61 (18): 6360–6370. doi:10.1021/jo960633p. ISSN 0022-3263. PMID 11667478. https://doi.org/10.1021/jo960633p. 
  3. ↑ Holm, R. H. (1987). "Metal-centered oxygen atom transfer reactions". Chem. Rev. 87 (6): 1401–1449. doi:10.1021/cr00082a005. 
  4. ↑ Meunier, Bernard; de Visser, Samuël P.; Shaik, Sason (2004). "Mechanism of Oxidation Reactions Catalyzed by Cytochrome P450 Enzymes". Chemical Reviews 104 (9): 3947–3980. doi:10.1021/cr020443g. ISSN 0009-2665. PMID 15352783. 
  5. ↑ Du, G.; Abu-Omar, M. M. (2008). "Oxo and Imido Complexes of Rhenium and Molybdenum in Catalytic Reductions". Current Organic Chemistry 12 (14): 1185–1198. doi:10.2174/138527208785740238. 
  6. ↑ 6.0 6.1 Gunay, A.; Theopold, K. H. (2010). "C-H Bond Activations by Metal Oxo Compounds". Chem. Rev. 110 (2): 1060–1081. doi:10.1021/cr900269x. PMID 20143877. 
  7. ↑ 7.0 7.1 Hay-Motherwell, Robyn S.; Wilkinson, Geoffrey; Hussain-Bates, Bilquis; Hursthouse, Michael B. (1993). "Synthesis and X-ray Crystal Structure of Oxotrimesityl-Iridium(V)". Polyhedron 12 (16): 2009–2012. doi:10.1016/S0277-5387(00)81474-6. 
  8. ↑ Huang, Xiongyi; Groves, John T. (2017). "Beyond Ferryl‑Mediated Hydroxylation: 40 Years of the rebound mechanism and C–H activation". J Biol Inorg Chem 22 (2–3): 185–207. doi:10.1007/s00775-016-1414-3. PMID 27909920. 
  9. ↑ Hausinger, R. P. (January–February 2004). "Fe(II)/α-Ketoglutarate-Dependent Hydroxylases and Related Enzymes". Crit. Rev. Biochem. Mol. Biol. 39 (1): 21–68. doi:10.1080/10409230490440541. PMID 15121720. 
  10. ↑ Ortiz de Montellano, Paul R. (2010). "Hydrocarbon Hydroxylation by Cytochrome P450 Enzymes". Chemical Reviews 110 (2): 932–948. doi:10.1021/cr9002193. ISSN 0009-2665. PMID 19769330. 
  11. ↑ Coon, M. J. (1998-01-20). "Epoxidation of olefins by cytochrome P450: Evidence from site-specific mutagenesis for hydroperoxo-iron as an electrophilic oxidant". Proceedings of the National Academy of Sciences 95 (7): 3555–60. doi:10.1073/pnas.95.7.3555. PMID 9520404. Bibcode: 1998PNAS...95.3555V. 
  12. ↑ Farinas, Edgardo T; Alcalde, Miguel; Arnold, Frances (2004). "Alkene epoxidation catalyzed by cytochrome P450 BM-3 139-3". Tetrahedron 60 (3): 525–528. doi:10.1016/j.tet.2003.10.099. ISSN 0040-4020. 
  13. ↑ Korzekwa, Kenneth; Trager, William; Gouterman, Martin; Spangler, Dale; Loew, Gilda (1985). "Cytochrome P450 mediated aromatic oxidation: a theoretical study". Journal of the American Chemical Society 107 (14): 4273–4279. doi:10.1021/ja00300a033. ISSN 0002-7863. 
  14. ↑ Brunold, T.C. (2007). "Synthetic Iron-Oxo 'Diamond Core' Mimics Structure of Key IIntermediate in Methane Monooxygenase Catalytic Cycle". Proc. Natl. Acad. Sci. U.S.A. 104 (52): 20641–20642. doi:10.1073/pnas.0710734105. PMID 18093936. Bibcode: 2007PNAS..10420641B. 
  15. ↑ Schwarz, G.; Mendel, R. R.; Ribbe, M. W. (2009). "Molybdenum Cofactors, Enzymes and Pathways". Nature 460 (7257): 839–847. doi:10.1038/nature08302. PMID 19675644. Bibcode: 2009Natur.460..839S. 
  16. ↑ Mukund, S.; Adams, M. W. W. (1996). "Molybdenum and Vanadium Do Not Replace Tungsten in the Catalytically Active Forms of the Three Tungstoenzymes in the Hyperthermophilic Archaeon Pyrococcus furiosus". J. Bacteriol. 178 (1): 163–167. doi:10.1128/jb.178.1.163-167.1996. PMID 8550411. 
  17. ↑ 17.0 17.1 Umena, Yasufumi; Kawakami, Keisuke; Shen, Jian-Ren; Kamiya, Nobuo (2011). "Crystal structure of oxygen-evolving photosystem II at a resolution of 1.9 Å". Nature 473 (7345): 55–60. doi:10.1038/nature09913. ISSN 0028-0836. PMID 21499260. Bibcode: 2011Natur.473...55U. http://ousar.lib.okayama-u.ac.jp/files/public/4/47455/20160528084139320094/Nature_473_55–60.pdf. 
  18. ↑ 18.0 18.1 18.2 Winkler, Jay R.; Gray, Harry B. (2012). "Electronic Structures of Oxo-Metal Ions". in Mingos, David Michael P.; Day, Peter; Dahl, Jens Peder. Molecular Electronic Structures of Transition Metal Complexes I. Structure and Bonding. 142. Springer Nature. pp. 17–28. doi:10.1007/430_2011_55. ISBN 978-3-642-27369-8. 
  19. ↑ Larson, Virginia A.; Battistella, Beatrice; Ray, Kallol; Lehnert, Nicolai; Nam, Wonwoo (2020). "Iron and manganese oxo complexes, oxo wall and beyond". Nature Reviews Chemistry 4 (8): 404–419. doi:10.1038/s41570-020-0197-9. 
  20. ↑ Anderson, Travis M.; Neiwert, Wade A.; Kirk, Martin L.; Piccoli, Paula M. B.; Schultz, Arthur J.; Koetzle, Thomas F.; Musaev, Djamaladdin G.; Morokuma, Keiji et al. (2004-12-17). "A Late-Transition Metal Oxo Complex: K7Na9[O=PtIV(H2O)L2, L = [PW9O34]9-"] (in en). Science 306 (5704): 2074–2077. doi:10.1126/science.1104696. ISSN 0036-8075. PMID 15564312. https://www.science.org/doi/10.1126/science.1104696. 
  21. ↑ Anderson, Travis M.; Cao, Rui; Slonkina, Elena; Hedman, Britt; Hodgson, Keith O.; Hardcastle, Kenneth I.; Neiwert, Wade A.; Wu, Shaoxiong et al. (2005-08-01). "A Palladium-Oxo Complex. Stabilization of This Proposed Catalytic Intermediate by an Encapsulating Polytungstate Ligand". Journal of the American Chemical Society 127 (34): 11948–11949. doi:10.1021/ja054131h. ISSN 0002-7863. PMID 16117527. https://doi.org/10.1021/ja054131h. 
  22. ↑ Cao, Rui; Anderson, Travis M.; Piccoli, Paula M. B.; Schultz, Arthur J.; Koetzle, Thomas F.; Geletii, Yurii V.; Slonkina, Elena; Hedman, Britt et al. (2007-09-01). "Terminal Gold-Oxo Complexes". Journal of the American Chemical Society 129 (36): 11118–11133. doi:10.1021/ja072456n. ISSN 0002-7863. PMID 17711276. https://doi.org/10.1021/ja072456n. 
  23. ↑ O’Halloran, Kevin P.; Zhao, Chongchao; Ando, Nicole S.; Schultz, Arthur J.; Koetzle, Thomas F.; Piccoli, Paula M. B.; Hedman, Britt; Hodgson, Keith O. et al. (2012). "Revisiting the Polyoxometalate-Based Late-Transition-Metal-Oxo Complexes: The "Oxo Wall" Stands". Inorganic Chemistry 51 (13): 7025–7031. doi:10.1021/ic2008914. PMID 22694272. 
  24. ↑ Ritter, Stephen K. (June 12, 2012). "Metal-Oxo Papers Retracted". https://cen.acs.org/articles/90/web/2012/06/Metal-Oxo-Papers-Retracted.html. 
  25. ↑ Hadlington2012-06-14T00:00:00+01:00, Simon. "Oxo wall still stands as inorganic papers retracted" (in en). https://www.chemistryworld.com/news/oxo-wall-still-stands-as-inorganic-papers-retracted/5108.article. 



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