Chemistry:Organorhenium chemistry

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Organorhenium chemistry describes the compounds with Re−C bonds. Because rhenium is a rare element, relatively few applications exist, but the area has been a rich source of concepts and a few useful catalysts.

General features

Rhenium exists in ten known oxidation states from −3 to +7 except −2, and all but Re(−3) are represented by organorhenium compounds. Most are prepared from salts of perrhenate and related binary oxides.[1] The halides, e.g., ReCl5 are also useful precursors as are certain oxychlorides.

A noteworthy feature of organorhenium chemistry is the coexistence of oxide and organic ligands in the same coordination sphere.[2]

Carbonyl compounds

Dirhenium decacarbonyl is a common entry point to other rhenium carbonyls. The general patterns are similar to the related manganese carbonyls. It is possible to reduce this dimer with sodium amalgam to Na[Re(CO)5] with rhenium in the formal oxidation state −1. Bromination of dirhenium decacarbonyl gives bromopentacarbonylrhenium(I),[3] then reduced with zinc and acetic acid to pentacarbonylhydridorhenium:[4]

Re2(CO)10 + Br2 → 2 Re(CO)5Br
Re(CO)5Br + Zn + HOAc → Re(CO)5H + ZnBr(OAc)

Bromopentacarbonylrhenium(I) is readily decarbonylated. In refluxing water, it forms the triaquo cation:[5]

Re(CO)5Br + 3 H2O → [Re(CO)3(H2O)3]Br + 2 CO

With tetraethylammonium bromide Re(CO)5Br reacts to give the anionic tribromide:[6]

Re(CO)5Br + 2 NEt4Br → [NEt4]2[Re(CO)3Br3] + 2 CO

Cyclopentadienyl complexes

One of the first transition metal hydride complexes to be reported was (C5H5)2ReH. A variety of half-sandwich compounds have been prepared from (C5H5)Re(CO)3 and (C5Me5)Re(CO)3. Notable derivatives include the electron-precise oxide (C5Me5)ReO3 and (C5H5)2Re2(CO)4.

Re-alkyl and aryl compounds

Structure of methylrhenium trioxide.

Rhenium forms a variety of alkyl and aryl derivatives, often with pi-donor coligands such as oxo groups. Well known is methylrhenium trioxide ("MTO"), CH3ReO3 a volatile, colourless solid, a rare example of a stable high-oxidation state metal alkyl complex. This compound has been used as a catalyst in some laboratory experiments. It can be prepared by many routes, a typical method is the reaction of Re2O7 and tetramethyltin:[7]

Re2O7 + (CH3)4Sn → CH3ReO3 + (CH3)3SnOReO3

Analogous alkyl and aryl derivatives are known. Although PhReO3 is unstable and decomposes at –30 °C, the corresponding sterically hindered mesityl and 2,6-xylyl derivatives (MesReO3 and 2,6-(CH3)2C6H3ReO3) are stable at room temperature. The electron poor 4-trifluoromethylphenylrhenium trioxide (4-CF3C6H4ReO3) is likewise relatively stable.[8] MTO and other organylrhenium trioxides catalyze oxidation reactions with hydrogen peroxide as well as olefin metathesis in the presence of a Lewis acid activator.[9] Terminal alkynes yield the corresponding acid or ester, internal alkynes yield diketones, and alkenes give epoxides. MTO also catalyses the conversion of aldehydes and diazoalkanes into an alkene.[10]

Rhenium is also able to make complexes with fullerene ligands such as Re2(PMe3)4H8(η2:η2C60).

Further reading

  • Synthesis of Organometallic Compounds: A Practical Guide Sanshiro Komiya Ed. S. Komiya, M. Hurano 1997.
  • Pericles Stavropoulos, Peter G. Edwards, Geoffrey Wilkinson, Majid Motevalli, K. M. Abdul Malik and Michael B. Hursthouse "Oxoalkyls of rhenium-(V) and-(VI). X-Ray crystal structures of (Me4ReO)2Mg(thf)4,[(Me3SiCH2)4ReO]2Mg(thf)2, Re2O3Me6 and Re2O3(CH2SiMe3)6" J. Chem. Soc., Dalton Trans., 1985, pp. 2167-2175. doi:10.1039/DT9850002167

References

  1. ↑ O. Glemser "Ammonium Perrhenate" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 1476-85.
  2. ↑ W. A. Herrmann and F. E. Kuhn (1997). "Organorhenium Oxides". Acc. Chem. Res. 30 (4): 169–180. doi:10.1021/ar9601398. 
  3. ↑ Schmidt, Steven P.; Trogler, William C.; Basolo, Fred (1990). Pentacarbonylrhenium Halides. Inorganic Syntheses. 28. pp. 154–159. doi:10.1002/9780470132593.ch42. ISBN 978-0-470-13259-3. 
  4. ↑ Michael A. Urbancic, John R. Shapley (1990). "Pentacarbonylhydridorhenium". Inorganic Syntheses. 28. pp. 165–168. doi:10.1002/9780470132593.ch43. ISBN 978-0-470-13259-3. 
  5. ↑ Lazarova, N.; James, S.; Babich, J.; Zubieta, J. (2004). "A convenient synthesis, chemical characterization and reactivity of [Re(CO)3(H2O)3]Br: the crystal and molecular structure of [Re(CO)3(CH3CN)2Br]". Inorganic Chemistry Communications 7 (9): 1023–1026. doi:10.1016/j.inoche.2004.07.006. 
  6. ↑ Alberto, R.; Egli, A.; Abram, U.; Hegetschweiler, K.; Gramlich V.; Schubiger, P. A. (1994). "Synthesis and reactivity of [NEt4]2[ReBr3(CO)3]. Formation and structural characterization of the clusters [NEt4][Re3(µ3-OH)(µ-OH)3(CO)9] and [NEt4][Re2(µ-OH)3(CO)6] by alkaline titration". J. Chem. Soc., Dalton Trans. (19): 2815–2820. doi:10.1039/DT9940002815. 
  7. ↑ Romão, Carlos C.; Kühn, Fritz E.; Herrmann, Wolfgang A. (1997). "Rhenium(VII) Oxo and Imido Complexes: Synthesis, Structures, and Applications". Chemical Reviews 97 (8): 3197–3246. doi:10.1021/cr9703212. PMID 11851489. 
  8. ↑ Dyckhoff, Florian; Li, Su; Reich, Robert M.; Hofmann, Benjamin J.; Herdtweck, Eberhardt; Kühn, Fritz E. (2018). "Synthesis, characterization and application of organorhenium(vii) trioxides in metathesis reactions and epoxidation catalysis" (in en). Dalton Transactions 47 (29): 9755–9764. doi:10.1039/c8dt02326c. ISSN 1477-9226. PMID 29987275. 
  9. ↑ Schmidt, Boris (1997). "Methyltrioxorhenium - from oxidation and cyclopropanation to metathesis" (in en). Journal für Praktische Chemie/Chemiker-Zeitung 339 (1): 493–496. doi:10.1002/prac.19973390190. ISSN 0941-1216. 
  10. ↑ Hudson, A. "Methyltrioxorhenium" Encyclopedia of Reagents for Organic Synthesis. John Wiley & Sons: New York, 2002.



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