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Discrete Heteroscorpionate Lithium and Zinc Alkyl Complexes. Synthesis, Structural Studies, and ROP of Cyclic Esters

2008; American Chemical Society; Volume: 27; Issue: 6 Linguagem: Inglês

10.1021/om701187s

1520-6041

Carlos Alonso‐Moreno, Andrés Garcés, Luis F. Sánchez‐Barba, Mariano Fajardo, Juan Fernández‐Baeza, Antonío Otero, Agustín Lara‐Sánchez, Antonío Antiñolo, L.M. Broomfield, I. López-Solera, Ana M. Rodrı́guez,

Organometallic Complex Synthesis and Catalysis

The reaction of bis(3,5-di-tert-butylpyrazol-1-yl)methane (bdtbpzm) with BunLi and carbodiimide derivatives, namely, N,N′-diisopropyl and 1-tert-butyl-3-ethyl carbodiimides, gives rise to the new sterically hindered lithium acetamidinate [Li(tbptamd)(THF)] (1) [tbptamd = N-ethyl-N′-tert-butylbis(3,5-di-tert-butylpyrazol-1-yl)acetamidinate] and [Li(pbptamd)(THF)] (2) [pbptamd = N,N′-diisopropylbis(3,5-di-tert-butylpyrazol-1-yl)acetamidinate]. Subsequent hydrolysis of 1 and 2, and the recently reported heteroscorpionate lithium salts [Li(tbpamd)(THF)] [tbpamd = N-ethyl-N′-tert-butylbis(3,5-dimethylpyrazol-1-yl)acetamidinate] and [Li(pbpamd)(THF)] [pbpamd = N,N′-diisopropylbis(3,5-dimethylpyrazol-1-yl)acetamidinate] with NH4Cl/H2O in ether cleanly affords the corresponding amidine ligands Htbpamd (3), Hpbpamd (4), Htbptamd (5), and Hpbptamd (6) in very good yields. The X-ray diffraction molecular structure of 3 was obtained. Reaction of the amidine-heteroscorpionate ligands 3–6 with 1 equiv of ZnR′2 proceeds in very high yields to give the neutral heteroscorpionate alkyl zinc complexes [Zn(R′)(NNN)] (NNN = tbpamd, R′ = Me 7, Et 8, CH2SiMe3 9; NNN = pbpamd, R′ = Me 10, Et 11, CH2SiMe3 12; NNN = tbptamd, R′ = Me 13, Et 14; NNN = pbptamd, R′ = Me 15, Et 16). The single-crystal X-ray structures of the derivatives 8, 12, 15, and 16 confirm a four-coordinative structure with the zinc metal center in a distorted tetrahedral geometry and the heteroscorpionate ligands arranged in κ3-coordination mode. The new lithium salts 1 and 2 and the alkyls 7–9, 13, and 14 can act as efficient single-component initiators for the ring-opening polymerization of ϵ-caprolactone and lactides over a wide range of temperatures. ϵ-Caprolactone is polymerized within minutes to give high-medium molecular weight polymers with medium broad values of polydispersities. Lactide afforded PLA materials with medium molecular weights and polydispersities as narrow as Mw/Mn = 1.05. Additionally, polymerization of l-lactide occurred without racemization in the propagation process and offered highly crystalline, isotactic poly(l-lactides) with high melting temperatures (Tm = 165 °C). rac-Lactide polymerization also produces enriched levels of heterotactic poly(lactide). Polymer end group analysis shows that the polymerization mediated by alkyl zinc complexes is initiated by alkyl transfer to monomer.