Metal cages, chiral

On the other hand, the use of the suitable combination of a metal salt, chiral ligand, and base promotes at low temperature the formation in situ of chiral A-metalated azomethine ylides from the corresponding iminoester and the subsequent selective cycloaddition onto the fullerene cage. Thus, the P,S chiral ligand Fesulphos along with copper(II) acetate directs the addition toward the formation of the stereoisomer (25, 55)-2-alkoxycarbonyl-5-arylpyrrolidino[3,4 l,2][60]fullerene with complete cis diasteroselectivity and enantiomeric excesses up to 93% (Scheme 34.9). 

Enantioselectivity control in a [2 + 2]-photocydoaddition reaction was achieved in a chiral, self-assembled host. Fluoranthenes and N-cyclohexylmaleimide underwent an intramolecular reaction in a cage made of M6L4, with the metal M being palladium (II) coordinated to a chiral diamine, and the ligand Lbeing2,4,6-tris(4 -pyridyl)-l,3,5-triazine. Up to 50% ee was observed [117]. 

Various strategies have been pursued in order to immobilise chiral epoxidation catalysts and these encompass covalent attachment to solid supports,[41] steric occlusion in nanosized cages of zeolites,[42 44] entrapment in a polydimethylsiloxane membrane145,461 and fluorous biphasic systems.1471 However, these approaches frequently require tedious ligand modifications and often lead to a marked decrease in both selectivity and activity of the transition metal catalyst. 

Figure 6.31 The structures of (a) dodeca-, (b) pentadeca-, and (c) octadeca-nuclear clusters templated by two IX4-H ions, a X5-X (X = C1, Br) ion, and Xe p r r r r r COj , respectively. Formal assembly of a 60-metal hydroxide complex featuring 26 vertex-sharing [Ln4(ti3-OH)4] cubane units. These cubane building blocks form six dodecanuclear squares and eight octadecanuclear hexagons [102]. (Redrawn from X. Kong et al, A chiral 60-metal sodaUte cage featuring 26 vertex-sharing [Er4(p.3-OH)4] cubanes, Journal of the American Chemical Society, 131, 6918-6919, 2009.)...

X-Ray structure analysis of 14a, 15a, and 15b has established the central adamantane cage which is characteristic of the unsolvated triamides [6, 8], Whereas there is little appreciable interaction between the periphery of the molecules in the structures of the t-butyl substituted species 15a and 15b, the two-coordinate Li-atoms are "internally solvated" by the phenyl groups in the chiral triamide 14a (Fig. 3). The orientation of the aryl rings towards the puckered six-membered (LiN)s-ring and the short contact between Li and C7 indicates a direct interaction between the metal atoms and the periphery. 

The cage confers interesting properties on the metal compared with the parent tris(ethylenediamine). For example, Co2+ does not exchange with the Co(II) cage in 24 hrs at 25° even though Co2+ usually exchanges its ligands on the microsecond time scale. Moreover, the Co(II) complex retains its chirality at least over... 

The ship-in-a-bottle technique is perhaps the most common method for encapsulation of transition metal complexes. In this way the tetradentate Schiff base ligand SALEN (bis-salicylidene) ethylenediamine can diffuse through the 12 MR windows of faujasite. Then, when complexed with a previously exchanged metal ion, nearly square planar coordination geometry is formed inside the a-cages [97-100], Mn complexes with a chiral ligand, prepared by the ship-in-a-bottle technique inside Y and EMT zeolites, have enantioselectively carried at the epoxidation of olefins [101,102]. 

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