Organochromium chemistry

Organochromium chemistry is a branch of organometallic chemistry that deals with organic compounds containing a chromium to carbon bond and their reactions.[1][2] The field is of some relevance to organic synthesis. The relevant oxidation states for chromium range from -2 to +6.

History

The first organochromium compound was described in 1919 by Franz Hein.[3] He treated phenylmagnesium bromide with chromium(III) chloride to give a new product (after hydrolysis) which he incorrectly identified as pentaphenyl chromium bromide (Ph5CrBr). Years later, in 1957 H.H. Zeiss et al. repeated Hein's experiments and correctly arrived at a cationic bisarene chromium sandwich compound (Ar2Cr+).[4] Bis(benzene)chromium itself was discovered around the same time in 1956 by Ernst Otto Fischer by reaction of chromium(III) chloride, benzene and aluminum chloride.[5][6] The related compound chromocene was discovered a few years earlier in 1953 also by Fischer.[7]

In another development, Anet and Leblanc also in 1957 prepared a benzyl chromium solution from benzyl bromide and chromium(II) perchlorate.[8] This reaction involves one-electron oxidative addition of the carbon-bromine bond, a process which was shown by Kochi[9][10] to be a case of double single electron transfer, first to give the benzyl free radical and then to the benzyl anion.

G. Wilke et al. introduced tris-(η-allyl)chromium in 1963 as an early Ziegler-Natta catalyst (but not successful in the long run)[11] Chromocene compounds were first employed in ethylene polymerization in 1972 by Union Carbide[12] and continue to used today in the industrial production of high-density polyethylene.

The organochromium compound (phenylmethoxycarbene)pentacarbonylchromium, Ph(OCH3)C=Cr(CO)5 was the first carbene complex to be crystallographically characterized by Fischer in 1967 (now called a Fischer carbene).[13] The first ever carbyne, this one also containing chromium, made its debut in 1973.[14]

The first example of a proposed metal-metal quintuple bond is found in a compound of the type [CrAr]2, where Ar is a bulky aryl ligand.

Applications in organic synthesis

Although organochromium chemistry is heavily employed in industrial catalysis, relatively few reagents have been developed for applications in organic synthesis. Two are the Nozaki-Hiyama-Kishi reaction (1977) (transmetallation with organonickel intermediate) and the Takai olefination (1986)(oxidation of Cr(II) to Cr(III) while replacing halogens). In a niche exploit, certain tricarbonyl(arene)chromium complexes display benzylic activation.

Organochromium compounds

Organochromium compounds can be divided into these broad compound classes:

Ethylene polymerization and oligomerization

Chromium catalysts are important in ethylene polymerization.[16] The Phillips catalyst is prepared by impregnating chromium(VI) oxide on silica followed activation in dry air at high temperatures. The bright yellow catalyst becomes reduced by the ethylene to afford a probable Cr(II) species that is catalytically active.[17] A related catalytic systems developed by Union Carbide and DSM are also based on silica with chromocene and other chromium complexes. How these catalysts work is unclear. One model system describes it as coordination polymerization:

With two THF ligands the catalyst is stable but in dichloromethane one ligand is lost to form a 13 electron chromium intermediate. This enables side-on addition of an ethylene unit and a polymer chain can grow by migratory insertion.

Chromium compounds also catalyse the trimerization of ethylene to produce the monomer 1-hexene.[18]

Comparisons with heavier group 6 organometallics

The heavier group 6 elements molybdenum and tungsten form organometallic compounds similar to those for chromium but also with differences. Whereas Cr(III) aquo alkyl compounds are well studied, the corresponding Mo(III) and W(III) compounds are not. Whereas chromocene is a stable compound, the related molybdenocene and tungstenocene are highly reactive. On the other hand, Mo and W readily form derivatives of the type Cp2MX2, whereas the smaller Cr does not form such clamshell compounds. Homoleptic alkyl and aryl complexes of the type R4M are rare, and hexamethyltungsten has no analogue in Cr chemistry.

Similar are the carbonyls such as molybdenum hexacarbonyl and tungsten hexacarbonyl and the related carbene and carbyne complexes. Compounds of the type [CpM(CO)3]2 are known for all three metals, e.g. Cyclopentadienylmolybdenum tricarbonyl dimer.[19] The chromium compound is however prone to homolysis of the Cr-Cr bond owing to steric crowding.

In the Kauffmann olefination, molybdenum(III) chloride and methyllithium form an organometallic complex capable of carbonyl olefination.

See also

CH He
CLi CBe CB CC CN CO CF Ne
CNa CMg CAl CSi CP CS CCl CAr
CK CCa CSc CTi CV CCr CMn CFe CCo CNi CCu CZn CGa CGe CAs style="background-color:#98FF98" border-collapse:collapse" | CSe CBr CKr
CRb CSr CY CZr CNb CMo CTc CRu CRh CPd CAg CCd CIn CSn CSb CTe CI CXe
CCs CBa CHf CTa CW CRe COs CIr CPt CAu CHg CTl CPb CBi CPo CAt Rn
Fr CRa Rf Db CSg Bh Hs Mt Ds Rg Cn Uut Fl Uup Lv Uus Uuo
↓
CLa CCe CPr CNd CPm CSm CEu CGd CTb CDy CHo CEr CTm CYb CLu
Ac CTh CPa CU CNp CPu CAm CCm CBk CCf CEs Fm Md No Lr
Chemical bonds to carbon
Core organic chemistry Many uses in chemistry
Academic research, but no widespread use Bond unknown

References

  1. ↑ Review: Carbon-Carbon Bond Formations Involving Organochromium(III) Reagents Furstner, A. Chem. Rev.; (Review); 1999; 99(4); 991-1046. doi:10.1021/cr9703360
  2. ↑ Review: From Hein to Hexene: Recent Advances in the Chemistry of Organochromium -Complexes Jolly, P. W. Acc. Chem. Res.; (Article); 1996; 29(11); 544-551. doi:10.1021/ar9502588
  3. ↑ Notiz über Chromorganoverbindungen (p 195-196) F. Hein Berichte der deutschen chemischen Gesellschaft (A and B Series) Volume 52, Issue 1 , Pages 195 - 196 1919 doi:10.1002/cber.19190520126
  4. ↑ π-Complexes of the Transition Metals. I. Hein's Polyaromatic Chromium Compounds Harold H. Zeiss, Minoru Tsutsui J. Am. Chem. Soc.; 1957; 79(12); 3062-3066. doi:10.1021/ja01569a019
  5. ↑ Zur Frage der Struktur der Chrom-phenyl-Verbindungen. Über Aromatenkomplexe von Metallen VI (p 1809-1815) E. Otto Fischer, Dietlinde Seus Chemische Berichte Volume 89, Issue 8 , Pages 1809 - 1815 1956 doi:10.1002/cber.19560890803
  6. ↑ Zur Frage der Struktur der Chrom-phenyl-Verbindungen. Bemerkungen zur Abhandlung von E. O. Fischer und D. Seus (p 1816-1821) Fr. Hein Chemische Berichte Volume 89, Issue 8 , Pages 1816 - 1821 1956 doi:10.1002/cber.19560890804
  7. ↑ Fischer, E. O.; Hafner, W. Z. Naturforsch. 1953, 8b, 444.
  8. ↑ F. A. L. Anet, E. Leblanc "A Novel Organochromium Compound" J. Am. Chem. Soc.; 1957; 79(10), 2649-2650. doi:10.1021/ja01567a080
  9. ↑ Reduction of Organic Halides by Chromium(II). Mechanism of the Formation of Benzylchromium Ion Jay K. Kochi, Dennis D. Davis J. Am. Chem. Soc.; 1964; 86(23); 5264-5271. doi:10.1021/ja01077a044
  10. ↑ Stereochemistry of reductive elimination by chromium(II) complexes Jay K. Kochi, David M. Singleton J. Am. Chem. Soc.; 1968; 90(6); 1582-1589. doi:10.1021/ja01008a032
  11. ↑ Wilke, G. Cyclooligomerisation von Butadien und Übergangsmetall--Komplexe Angewandte Chemie, 1963 Volume 75, pp. 10-20. doi:10.1002/ange.19630750104
  12. ↑ Frederick J. Karol, George L. Karapinka, Chisung Wu, Alan W. Dow, Robert N. Johnson, Wayne L. Carrick Chromocene catalysts for ethylene polymerization: Scope of the polymerization Journal of Polymer Science Part A-1: Polymer Chemistry 1972 Volume 10, Issue 9, pp. 2621-2637. doi:10.1002/pol.1972.150100910
  13. ↑ Ernst Otto Fischer, Alfred Maasböl Übergangsmetall-Carben-Komplexe, II. Phenylmethoxycarben- und Methylmethoxycarben-pentacarbonyl-chrom, -molybdän, -wolfram und -cyclopentadienyl-dicarbonyl-mangan Chemische Berichte 1967 Volume 100, pp. 2445-2456 doi:10.1002/cber.19671000744
  14. ↑ Ernst Otto Fischer, Gerhard Kreis, Cornelius G. Kreiter, Jörn Mülle, Gottfried Huttner, Hans Lorenz trans-Halogeno-alkyl(aryl)carbin-tetracarbonyl-Komplexe von Chrom, Molybdän und Wolfram-Ein neuer Verbindungstyp mit Übergangsmetall-Kohlenstoff-Dreifachbindung Angewandte Chemie 1973, Volume 85, Issue 14, p 618-620. doi:10.1002/ange.19730851407
  15. ↑ James H. Espenson Chemistry of Organochromium(III) Complexes Acc. Chem. Res.; 1992, volume 25, pp. 222-227. doi:10.1021/ar00017a003
  16. ↑ Klaus H. Theopold Organochromium(III) chemistry: a neglected oxidation state Acc. Chem. Res. 1990, volume 23, pp. 263-270. doi:10.1021/ar00176a005
  17. ↑ Kenneth S. Whiteley,T. Geoffrey Heggs, Hartmut Koch, Ralph L. Mawer, Wolfgang Immel, "Polyolefins" in Ullmann's Encyclopedia of Industrial Chemistry 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a21_487
  18. ↑ John T. Dixon, Mike J. Green, Fiona M. Hess, David H. Morgan “Advances in selective ethylene trimerisation – a critical overview” Journal of Organometallic Chemistry 2004, Volume 689, Pages 3641-3668. doi:10.1016/j.jorganchem.2004.06.008
  19. ↑ Synthesis of Organometallic Compounds: A Practical Guide Sanshiro Komiya Ed. S. Komiya, M. Hurano 1997
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