Trisoxazolinylborate

Trisoxazolinylborate ligand

Tris(oxazolinyl)borate compounds are a class of tridentate ligands; often abbreviated To^R, where R is the substituent on the oxazoline ring. Most commonly the substituent is either a methyl, propyl, tert-butyl or hydrogen. The formation of anionic boron backbone with addition of a phenyl group on boron allows the ligand to strongly bind to the metal center. It results in a more robust complex.^[1]

Tris(oxazolinyl)borates can be characterised as scorpionate ligands and may be compared to tris(pyrazolyl)borate and trisoxazoline ligands. In bulky pyrazolylborate (Tp) derivatives, isomerization may occur via 1,2-shifts; additionally B–N bond cleavage is a common decomposition pathways for the Tp ligands. The oxazoline-based ligands with B-C linkages avoid these decomposition problems.^[1]

Synthesis

Tris(4,4-dimethyl-2-oxazolinyl)phenyl borate (To^M)

Tris(4S-isopropyl-2-oxazolinyl)phenylborate (To^P)

The first example of a trisoxazolinylborate ligand was tris(4,4-dimethyl-2-oxazolinyl)phenyl borate (To^M). This was prepared by a reaction of dichlorophenylborane with 3 equivalents of 2-lithio-4,4-dimethyl-2-oxazolide.^[2] Later variants, such as tris(4S-isopropyl-2-oxazolinyl)phenylborate (To^P) have been prepared in an analogous manner.^[3]

PhBCl₂ + 3 Li(Oxaz-Me₂) → PhB(Oxaz-Me₂)₃ + 3 LiCl

Complexes of To^R

The first coordination complexes made using To^M ligands were based around zirconium (IV), as the sterically bulky ligands were able to stabilise the highly reactive metal centers. To^MZr(IV) complexes were prepared by salt metathesis using LiTo^M and TlTo^M and ZrCl₄. The formed complex To^MZrCl₃ was found to be quite robust and showed C₃V symmetry in both solution and solid state.^[4]

Preparation of (To^M)ZrCl₃ ligand

Lithium tris(4,4-dimethyl-2-oxazolin-2-yl) phenyl borate (LiTo^M) is used as a transfer agent. However TlTo^M frequently is as a more effective transfer agent than LiTo^M because of the higher solubility of the Tl salt and the insolubility of thallium chloride by-products. In contrast, lithium halide byproducts from preparations employing LiTo^M can cause purification problems.^[1]

Another example for the coordinating chemistry of To^M is the formation of To^MMgMe by the reaction of equimolar amounts of HTo^M and MgMe²(O₂C₄H₈)₂. In addition, the reaction of two equivalents of HTo^M with MgMe₂(O₂C₄H₈)₂ gives the homoleptic To^M₂Mg compound. This compound can also be obtained by the reaction between one equivalent of HTo^M and To^MMgMe revealing that Mg in To^MMgMe is an active center for the chemical reactions. According to 1H NMR spectroscopic data, To^M₂Mg shows C_s symmetry. In these reactions HTo^M is used as the transfer agent.^[2] Coordination chemistry of iridium(I) centers with To^P has been shown by the preparation of [Ir(To^P)(COD)] (COD =1,5-C₈H₁₂) by the reaction of LiTo^P and 0.5 equivalent of [Ir(µ-Cl)(COD)]₂.^[3]

Preparation of (To^M)₂Mg ligand

Catalysis

To^MMgMe is an effective precatalyst for the cross-dehydrocoupling of Si-H bonds in organosilanes and N-H bonds in amines to give Si-N bonds and H₂.^[2] Furthermore, tris(oxazolinyl)borate yttrium alkyl and amide compounds (To^MYR₂) can be used as precatalysts for the cyclization of aminoalkenes.^[5]

See also

• Trisoxazolines
• Trispyrazolylborate

References

1. ↑ 1.0 1.1 1.2 Dunne, J.F. (2011). "Stoichiometric and catalytic reactivity of tris(oxazolinyl)borate main group metal compounds.".
2. ↑ 2.0 2.1 2.2 Dunne, J.F.; Neal, S.R; Engelkemier, J; Arkady, E; Sadow, A.D. (2011). "Tris(oxazolinyl)boratomagnesium-Catalyzed Cross-Dehydrocoupling of Organosilanes with Amines, Hydrazine, and Ammonia". J. Am. Chem. Soc. 133: 16782. doi:10.1021/ja207641b.
3. ↑ 3.0 3.1 Baird, Benjamin; Pawlikowski, A.V; Su, J; Wiencg, J.W; Pruski, M; Sadow, A.D. (2008). "Easily Prepared Chiral Scorpionates: Tris(2-oxazolinyl)boratoiridium(I) Compounds and Their Interactions with MeOTf". Inorg. Chem. 47: 10208. doi:10.1021/ic801637s.
4. ↑ Dunne, J.F.; Su, J; Ellern, A; Sadow, A.D. (2008). "A New Scorpionate Ligand: Tris(4,4-dimethyl-2-oxazolinyl)borate and Its Zirconium(IV) Complexes". Organometallics 27: 2399. doi:10.1021/om800252p.
5. ↑ Pawlikowski, A.V.; Ellern, A; Sadow, A.D. (2009). "Ligand Exchange Reactions and Hydroamination with Tris(oxazolinyl)borato Yttrium Compounds". Organometallics 27: 8020. doi:10.1021/ic900689k.