Alternating Copolymerization of CO2 and Cyclohexene Oxide by New Pyridylamidozinc(II) Catalysts
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作者:
D'Auria, Ilaria
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Univ Salerno, Dipartimento Chim & Biol A Zambelli, Via Giovanni Paolo II 132, I-84084 Fisciano, SA, ItalyUniv Salerno, Dipartimento Chim & Biol A Zambelli, Via Giovanni Paolo II 132, I-84084 Fisciano, SA, Italy
D'Auria, Ilaria
[1
]
D'Alterio, Massimo Christian
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Univ Salerno, Dipartimento Chim & Biol A Zambelli, Via Giovanni Paolo II 132, I-84084 Fisciano, SA, Italy
Univ Federico II Napoli, Dipartimento Sci Chim, Complesso Monte St Angelo,Via Cintia 21, I-80126 Naples, ItalyUniv Salerno, Dipartimento Chim & Biol A Zambelli, Via Giovanni Paolo II 132, I-84084 Fisciano, SA, Italy
D'Alterio, Massimo Christian
[1
,2
]
Talarico, Giovanni
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Univ Federico II Napoli, Dipartimento Sci Chim, Complesso Monte St Angelo,Via Cintia 21, I-80126 Naples, ItalyUniv Salerno, Dipartimento Chim & Biol A Zambelli, Via Giovanni Paolo II 132, I-84084 Fisciano, SA, Italy
Talarico, Giovanni
[2
]
Pellecchia, Claudio
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Univ Salerno, Dipartimento Chim & Biol A Zambelli, Via Giovanni Paolo II 132, I-84084 Fisciano, SA, ItalyUniv Salerno, Dipartimento Chim & Biol A Zambelli, Via Giovanni Paolo II 132, I-84084 Fisciano, SA, Italy
Pellecchia, Claudio
[1
]
机构:
[1] Univ Salerno, Dipartimento Chim & Biol A Zambelli, Via Giovanni Paolo II 132, I-84084 Fisciano, SA, Italy
[2] Univ Federico II Napoli, Dipartimento Sci Chim, Complesso Monte St Angelo,Via Cintia 21, I-80126 Naples, Italy
Five new Zn(II) complexes bearing pyridylamido ligands with different substituents at the pyridine and at the amido moieties were synthesized and evaluated as catalysts for the alternating copolymerization of carbon dioxide and cyclohexene oxide. Polymers with carbonate linkages ranging between 86 and 99% and a slightly isotacticenriched structure were selectively obtained under a variety of reaction conditions, including 1 atm of CO2 pressure, without any cocatalyst. Some experimental and theoretical evidence suggested that different initiating species are involved in the catalytic cycle, including dimeric [(L-x)Zn(mu-OR)](2) and [(L-x)Zn(mu-O2COR)] complexes similar to those involved in the classical beta-diiminate Zn(II) catalysts.
机构:
Univ Tokyo, Grad Sch Engn, Dept Chem & Biotechnol, Bunkyo Ku, Tokyo 1138656, JapanUniv Tokyo, Grad Sch Engn, Dept Chem & Biotechnol, Bunkyo Ku, Tokyo 1138656, Japan
Nakano, K
Hiyama, T
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机构:Univ Tokyo, Grad Sch Engn, Dept Chem & Biotechnol, Bunkyo Ku, Tokyo 1138656, Japan
Hiyama, T
Nozaki, K
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机构:Univ Tokyo, Grad Sch Engn, Dept Chem & Biotechnol, Bunkyo Ku, Tokyo 1138656, Japan