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Organoniobium chemistry is the chemistry of compounds containing niobium-carbon (Nb-C) bonds. Compared to the other group 5 transition metal organometallics, the chemistry of organoniobium compounds most closely resembles that of organotantalum compounds. Organoniobium compounds of oxidation states +5, +4, +3, +2, +1, 0, -1, and -3 have been prepared, with the +5 oxidation state being the most common.[1]
Compound classes
[edit]Carbonyls
[edit]Unlike vanadium, the neutral binary carbonyl of niobium is unstable. The salts of the anionionic binary carbonyls, exemplified by [Nb(CO)6]−, can be obtained by reduction of NbCl5 under an atmosphere of CO. Heteroleptic niobium carbonyls supported by Cp ligands can be prepared at various oxidation states of Nb and serve as useful precursors in niobium carbonyl chemistry.[2]
Alkyl
[edit]A wide variety of alkyl Nb compounds have been prepared. Low coordination number complexes require the absence of any β-hydrogen to prevent rapid β-hydride elimination to the electron poor metal center.[3] The simplest compounds are salts of [Nb(CH3)6]−. It is prepared by alkylation of NbF5 using methyl lithium:[4]
- NbF5 + 6 LiCH3 → Li[Nb(CH3)6] + 5 LiF
Alkylidenes
[edit]Along with the related organotantalum species, niobium alkylidenes were among the first Scrock carbenes studied. The first syntheses of these complexes involved addition of organolithium reagents lacking β-hydrogens into hindered Nb(V) complexes followed by α-proton elimination. As compared to tantalum alkylidenes, niobium alkylidenes are less thermally and hydrolytically stable.[5]
Cyclopentadienyl derivatives
[edit]The first organoniobium coumpound fully characterized was Cp2NbBr3[6], however the paramagnetic Nb(IV) metallocenes such as niobocene dichloride are more prevalent. Complexes are typically prepared by treatment of NbCl5 with NaCp to form the bis(cyclopentadienyl) complex followed by further functionalization. Derivatives of pentamethylcyclopentadiene are also known, such as (C5Me5)2NbH3.[3]
Alkyne complexes
[edit]Similar to other d2 transition metals, Nb(III) alkyne complexes oxidatively insert to produce Nb(V) alkenediyl complexes. The Nb metallocyclopropenes thus formed feature improved thermal stability relative to other organometallics and are more readily characterized and used as synthetic intermediates[7]
Applications
[edit]While there are currently no reported commercial applications of organoniobium compounds, they have found some use in organic synthesis.
Studies on catalytic reaction mechanisms
[edit]Orbanoniobium compounds has served as a useful models for studying catalytic reaction mechanisms. While the high oxophilicity of Nb prevents its use as a CO reduction catalyst, neobium carbonyl complexes have been used to a a tool study individual steps in Fischer-Tropsch chemistry.[1]
Stoicheometric niobium reagents
[edit]A prominent early synthetic application of organoniobium chemsitry was the use of NbCl3(DME) as a reagent for the reductive coupling of imines with carbonyl compounds to form amino alcohols.[8] This reagent has found further use in other pinacol type reductive couplings.[9][10]
Nb(V) alkendiyl complexes have found use as latent dianion equivalents in synthetic reactions. Reduction of alkynes with Nb(III) compounds followed by trapping with suitable electrophiles has allowed the synthesis of various alkenes.[7][10]
Catalytic niobium reactions
[edit]A number of formal [2+2+2] cycloadditions have been realized under Nb catalysis, including alkyne trimerizations and couplings of alkynes with alkenes or nitriles to form cyclohexadienes or pyridines, respectively. Typically a Nb(III) catalyst will form a Nb(V) metallocyclopropene with a terminal alkyne component and then engage in sequential migratory insertions and reductive elimination to furnish the six membered ring and regenerate the Nb(III).[10]
An organoniobium catalyst has also been developed for (Z)-selective semihydrogenation of alkynes. The mechanistic pathway for this reaction is distinct from other transition metal catalyzed hydrogenations, proceeding through the Nb(V) metallocyclopropene which engages with hydrogen either through direct sigma-bond metathesis or outer sphere 1,2-addition.[11]
References
[edit]- ^ a b Waters, T.; Wedd, A. G.; Ziolek, M.; Nowak, I. (2004). Niobium and Tantalum. Vol. Vol. 4 (2nd ed.). Oxford: Elsevier. pp. 241–312. ISBN 0-08-0443265.
{{cite book}}:|volume=has extra text (help);|work=ignored (help) - ^ Wigley, D. E.; Gray, S. D. (1995). Niobium and Tantalum. Vol. Vol. 5 (2nd ed.). Oxford: Pergamon. pp. 57–154. ISBN 0-08-042312-4.
{{cite book}}:|volume=has extra text (help);|work=ignored (help) - ^ a b Labinger, J. A. (1982). Niobium and Tantalum. Vol. Vol. 3 (1st ed.). Oxford: Pergamon. pp. 705–782. ISBN 0-08-025269-9.
{{cite book}}:|volume=has extra text (help);|work=ignored (help) - ^ 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.
- ^ Schrock, Richard R. (1979). "Alkylidene complexes of niobium and tantalum". Accounts of Chemical Research. 12 (3): 98–104. doi:10.1021/ar50135a004. ISSN 0001-4842.
- ^ Wilkinson, G.; Birmingham, J. M. (1954). "Bis-cyclopentadienyl Compounds of Ti, Zr, V, Nb and Ta". Journal of the American Chemical Society. 76 (17): 4281–4284. doi:10.1021/ja01646a008. ISSN 0002-7863.
- ^ a b Parker, Kyle D. J.; Fryzuk, Michael D. (2015-06-08). "Synthesis, Structure, and Reactivity of Niobium and Tantalum Alkyne Complexes". Organometallics. 34 (11): 2037–2047. doi:10.1021/om5010385. ISSN 0276-7333.
- ^ Roskamp, Eric J.; Pedersen, Steven F. (1987). "The first practical niobium(III) reagent in organic synthesis. A convenient route to 2-amino alcohols via the coupling of imines with aldehydes or ketones promoted by NbCl3(DME)". Journal of the American Chemical Society. 109 (21): 6551–6553. doi:10.1021/ja00255a073. ISSN 0002-7863.
- ^ Kammermeier, Bernhard; Beck, Gerhard; Holla, Wolfgang; Jacobi, Detlev; Napierski, Bernd; Jendralla, Heiner (1996). "Vanadium(II)- and Niobium(III)-Induced, Diastereoselective Pinacol Coupling of Peptide Aldehydes to Give aC2-Symmetrical HIV Protease Inhibitor". Chemistry - A European Journal. 2 (3): 307–315. doi:10.1002/chem.19960020312.
- ^ a b c Satoh, Yasushi; Obora, Yasushi (2015). "Niobium Complexes in Organic Transformations: From Stoichiometric Reactions to Catalytic [2+2+2] Cycloaddition Reactions: Niobium Complex Organic Chemistry". European Journal of Organic Chemistry. 2015 (23): 5041–5054. doi:10.1002/ejoc.201500358.
- ^ Beaumier, Evan P.; Pearce, Adam J.; See, Xin Yi; Tonks, Ian A. (2019). "Modern applications of low-valent early transition metals in synthesis and catalysis". Nature Reviews Chemistry. 3 (1): 15–34. doi:10.1038/s41570-018-0059-x. ISSN 2397-3358. PMC 6462221. PMID 30989127.
{{cite journal}}: CS1 maint: PMC format (link)