Jump to content

Organotantalum chemistry

From Wikipedia, the free encyclopedia
Tantalum-Carbon Bond

Organotantalum chemistry is the chemistry of chemical compounds containing a carbon-to-tantalum chemical bond. A wide variety of compound have been reported, initially with cyclopentadienyl and CO ligands. Oxidation states vary from Ta(V) to Ta(-I).

Classes of organotantalum compounds

[edit]
Structure of [Li(OEt2)3]+[TaMe6]−.

Alkyl and aryl complexes

[edit]

Pentamethyltantalum was reported by Richard Schrock in 1974.[1]

Salts of [Ta(CH3)6]− are prepared by alkylation of TaF5 using methyl lithium:[2]

TaF5 + 6 LiCH3 → Li[Ta(CH3)6] + 5 LiF

Alkylidene complexes

[edit]

Tantalum alkylidene complexes arise by treating trialkyltantalum dichloride with alkyl lithium reagents. This reaction initially forms a thermally unstable tetraalkyl-monochloro-tantalum complex, which undergoes α-hydrogen elimination, followed by alkylation of the remaining chloride.[1]

Tantalum alkylidine synthesis
Synthesis of Tantalum Monoalkylidene Complexes

Tantalum alkylidene complexes are nucleophilic.[1] They effect a number of reactions including: olefinations, olefin metathesis, hydroaminoalkylation of olefins, and conjugate allylation of enones.

Tantalum Alkylidene Promoted Olefination

Ethylene, propylene, and styrene react with tantalum alkylidene complexes to yield olefin metathesis products.[3]

Cyclopentadienyl complexes

[edit]

Some of the first reported organotantalum complexes were cyclopentadienyl derivatives. These arise from the salt metathesis reactions of sodium cyclopentadienide and tantalum pentachloride. An example of this is the first transition metal trihydride, Cp2TaH3. More soluble and better developed are derivatives of pentamethylcyclopentadiene such as Cp*TaCl4, Cp*2TaCl2, and Cp*2TaH3.[4]

Tantalum Alkylidene Olefin Metathesis

Tantalum carbonyls and isocyanides

[edit]

Reduction of TaCl5 under an atmosphere of CO gives the salts of [Ta(CO)6]−.[5] These same anions can be obtained by carbonylation of tantalum arene complexes.

A number of tantalum isocyanide complexes are also known.[6]

Tantalum arenes and alkyne complexes

[edit]

Treatment of tantalum pentachloride with hexamethylbenzene (C6Me6), aluminium, and aluminium trichloride gives [M(η6-C6Me6)AlCl4]2.[7]

Tantalum-alkyne complexes[8] catalyze cyclotrimerizations.[9][10] Some tantalum-alkyne complexes are precursors to allylic alcohols.[11] Tantalacyclopropenes are invoked as intermediates.

Utimoto's Synthesis of (E)-Allylic Alcohols

Tantalum-amido complexes

[edit]

Organotantalum compounds are invoked as intermediates in C-alkylation of secondary amines with 1-alkenes using Ta(NMe2)5.[12] The chemistry developed by Maspero was later brought to fruition when Hartwig and Herzon reported the hydroaminoalkylation of olefins to form alkylamines:[13]

Hartwig hydroaminoalkylation reaction scheme

The catalytic cycle may proceed by β-hydrogen abstraction of the bisamide, which forms the metallaaziridine. Subsequent olefin insertion, protonolysis of the tantalum-carbon bond, and β-hydrogen abstraction affords the alkylamine product.[14][15][16]

Purposed mechanism of hydroaminoalkylation

Transmetalation

[edit]

Organotantalum reagents arise via transmetalation of organotin compounds with tantalum(V) chloride.[17] These organotantalum reagents promote the conjugate allylation of enones. Although the direct allylation of carbonyl groups is prevalent throughout the literature, little has been reported on the conjugate allylation of enones.[18]

Applications

[edit]

Organotantalum compounds are of academic interest, but few or no commercial applications have been described.

References

[edit]
  1. ^ a b c Schrock, Richard R. (1979-03-01). "Alkylidene complexes of niobium and tantalum". Accounts of Chemical Research. 12 (3): 98–104. doi:10.1021/ar50135a004. ISSN 0001-4842.
  2. ^ Kleinhenz, S.; Pfennig, V.; Seppelt, K. (1998). "Preparation and Structures of [W(CH3)6], [Re(CH3)6], [Nb(CH3)6]−, and [Ta(CH3)6]−". Chem. Eur. J. 4 (9): 1687. doi:10.1002/(SICI)1521-3765(19980904)4:9<1687::AID-CHEM1687>3.0.CO;2-R.
  3. ^ McLain, S. J.; Wood, C. D.; Schrock, R. R. (1977-05-01). "Multiple metal-carbon bonds. 6. The reaction of niobium and tantalum neopentylidene complexes with simple olefins: a route to metallocyclopentanes". Journal of the American Chemical Society. 99 (10): 3519–3520. doi:10.1021/ja00452a064. ISSN 0002-7863.
  4. ^ Endy Y.-J. Min; John E. Bercaw (2014). "Bis(η 5 -Pentamethylcyclopentadienyl) Complexes of Niobium and Tantalum". Inorganic Syntheses: Volume 36. Vol. 36. pp. 52–57. doi:10.1002/9781118744994.ch11. ISBN 978-1-118-74499-4. {{cite book}}: |journal= ignored (help)
  5. ^ J. E. Ellis; A. Davison (1976). "Tris[Bis(2-Methoxyethyl)Ether]Potassium and Tetraphenylarsonium Hexacarbonylmetallates(1-) of Niobium and Tantalum". Tris[Bis(2-Methoxyethyl)Ether]Potassium and Tetraphenylarsonium Hexacarbonylmetallates(1–) of Niobium and Tantalum. Inorganic Syntheses. Vol. 16. pp. 68–73. doi:10.1002/9780470132470.ch21. ISBN 978-0-470-13247-0.
  6. ^ Brennessel, William W.; Romanenkov, Alexander; Young, Victor G.; Ellis, John E. (2019). "Tantalum isocyanide complexes: TaI(CNDipp)6 (Dipp is 2,6-diisopropylphenyl) and ionic [Ta(CNDipp)7][Ta(CNDipp)6], a formal disproportionation product of the 17-electron Ta0 metalloradical Ta(CNDipp)6". Acta Crystallographica Section C: Structural Chemistry. 75 (2): 135–140. doi:10.1107/S2053229619000834. PMID 30720451. S2CID 73450348.
  7. ^ Pampaloni, G. (2010). "Aromatic hydrocarbons as ligands. Recent advances in the synthesis, the reactivity and the applications of bis(η6-arene) complexes". Coordination Chemistry Reviews. 254 (5–6): 402–419. doi:10.1016/j.ccr.2009.05.014.
  8. ^ Labinger, Jay A.; Schwartz, Jeffrey; Townsend, John M. (1974-06-01). "Iodo- and hydridotantalum(III) complexes of dialkylacetylenes". Journal of the American Chemical Society. 96 (12): 4009–4011. doi:10.1021/ja00819a047. ISSN 0002-7863.
  9. ^ Cotton, F. Albert; Hall, William T. (1979-08-01). "Reactions of tantalum(III) with alkynes and nitriles". Journal of the American Chemical Society. 101 (17): 5094–5095. doi:10.1021/ja00511a064. ISSN 0002-7863.
  10. ^ Bruck, M. A.; Copenhaver, A. S.; Wigley, D. E. (1987-10-01). "Alkyne cyclizations at reduced tantalum centers: synthesis and molecular structure of (.eta.6-C6Me6)Ta(O-2,6-i-Pr2C6H3)2Cl". Journal of the American Chemical Society. 109 (21): 6525–6527. doi:10.1021/ja00255a056. ISSN 0002-7863.
  11. ^ Takai, Kazuhiko; Kataoka, Y.; Utimoto, K. (1990-03-01). "Tantalum-alkyne complexes as synthetic intermediates. Stereoselective preparation of trisubstituted allylic alcohols from acetylenes and aldehydes". The Journal of Organic Chemistry. 55 (6): 1707–1708. doi:10.1021/jo00293a008. ISSN 0022-3263.
  12. ^ Clerici, Mario G.; Maspero, Federico (1980-01-01). "Catalytic C-Alkylation of Secondary Amines with Alkenes". Synthesis. 1980 (4): 305–306. doi:10.1055/s-1980-29002. ISSN 0039-7881. S2CID 94579838.
  13. ^ Herzon, Seth B.; Hartwig, John F. (2007-05-01). "Direct, Catalytic Hydroaminoalkylation of Unactivated Olefins with N-Alkyl Arylamines". Journal of the American Chemical Society. 129 (21): 6690–6691. doi:10.1021/ja0718366. ISSN 0002-7863. PMC 2590937. PMID 17474747.
  14. ^ Eisenberger, Patrick; Ayinla, Rashidat O.; Lauzon, Jean Michel P.; Schafer, Laurel L. (2009-10-19). "Tantalum–Amidate Complexes for the Hydroaminoalkylation of Secondary Amines: Enhanced Substrate Scope and Enantioselective Chiral Amine Synthesis". Angewandte Chemie International Edition. 48 (44): 8361–8365. doi:10.1002/anie.200903656. ISSN 1521-3773. PMID 19787670.
  15. ^ Dörfler, Jaika; Doye, Sven (2014-05-01). "A Commercially Available Tantalum Catalyst for the Highly Regioselective Intermolecular Hydroaminoalkylation of Styrenes". European Journal of Organic Chemistry. 2014 (13): 2790–2797. doi:10.1002/ejoc.201400082. ISSN 1099-0690.
  16. ^ Payne, Philippa R.; Garcia, Pierre; Eisenberger, Patrick; Yim, Jacky C.-H.; Schafer, Laurel L. (2013-05-03). "Tantalum Catalyzed Hydroaminoalkylation for the Synthesis of α- and β-Substituted N-Heterocycles". Organic Letters. 15 (9): 2182–2185. doi:10.1021/ol400729v. ISSN 1523-7060. PMID 23600625.
  17. ^ Shibata, Ikuya; Kano, Takeyoshi; Kanazawa, Nobuaki; Fukuoka, Shoji; Baba, Akio (2002-04-15). "Generation of Organotantalum Reagents and Conjugate Addition to Enones". Angewandte Chemie. 114 (8): 1447–1450. doi:10.1002/1521-3773(20020415)41:8<1389::AID-ANIE1389>3.0.CO;2-D. ISSN 1521-3757. PMID 19750774.
  18. ^ Yamamoto, Yoshinori; Asao, Naoki (1993-09-01). "Selective reactions using allylic metals". Chemical Reviews. 93 (6): 2207–2293. doi:10.1021/cr00022a010. ISSN 0009-2665.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Organotantalum_chemistry&oldid=1230402085"