Aluminum complexes containing biphenolate phosphine ligands: synthesis and living ring-opening polymerization catalysisElectronic supplementary information (ESI) available. CCDC 1479859 and 1479860. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6dt02143c
This report describes the synthesis, structure, and reactivity of aluminum complexes containing tridentate biphenolate phosphine ligands of the type [RP(2-O-3,5-C 6 H 2 t Bu 2 ) 2 ] 2− (R = t Bu ( 2a ), Ph ( 2b )). Alkane elimination of AlMe 3 with one equiv. of H 2 [ 2a ] or H 2 [ 2b ] in THF at 0...
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Zusammenfassung: | This report describes the synthesis, structure, and reactivity of aluminum complexes containing tridentate biphenolate phosphine ligands of the type [RP(2-O-3,5-C
6
H
2
t
Bu
2
)
2
]
2−
(R =
t
Bu (
2a
), Ph (
2b
)). Alkane elimination of AlMe
3
with one equiv. of H
2
[
2a
] or H
2
[
2b
] in THF at 0 °C cleanly affords colorless crystalline [
2a
]AlMe(THF) (
3a
) and [
2b
]AlMe(THF) (
3b
), respectively. An X-ray diffraction study of
3a
showed it to be a five-coordinate THF-bound species, whose coordination geometry is best described as trigonal bipyramidal, having the phosphorus donor and THF at axial positions. Treatment of either
in situ
prepared or isolated methyl complexes
3a,b
with one equiv. of benzyl alcohol in toluene or THF generated their corresponding benzyloxides {[
2a,b
]Al(μ
2
-OCH
2
Ph)}
2
(
4a,b
). An X-ray diffraction study of
4a
revealed a dimeric structure, in which the coordination geometry of aluminum is also distorted trigonal bipyramidal with the tridentate
2a
ligand being facially bound. In the presence of one equiv. of benzyl alcohol, complex
3a
is a competent catalyst precursor for the living ring-opening polymerization of -caprolactone ( -CL) and
rac
-lactide (
rac
-LA), producing poly( -caprolactone) and poly(
rac
-lactide), respectively, in a controlled manner. As such, well-defined block copolymers of -CL with
rac
-LA can also be prepared by catalytic
3a
. Kinetic studies revealed that
3a
catalyzes the polymerization of
rac
-lactide at a rate 2-fold faster than that of
3b
, indicating the significance of the
P
-substituent effect on this catalysis. Interestingly, the polymerization rate of
rac
-lactide by
3a
is 16.5 times faster than that of
l
-lactide under otherwise identical conditions.
The first examples of aluminum complexes containing biphenolate phosphine ligands are prepared, structurally characterized, and demonstrated to have catalytic competence in the living ring-opening (co)polymerization of -caprolactone and
rac
-lactide. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c6dt02143c |