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Synthesis of Trimeric Organozinc Compounds and their Subsequent Reaction with Oxygen.


ABSTRACT: A conventional solution-based route to a cyclic trimeric organozinc compound [{Zn(Et)(?-diketonate)}3] (?-diketonate=OC(OMe)CHC(Me)O, 1) is described, with 1 structurally characterized for the first time. The ligand selection of bidentate ?-diketonates is shown to be key to isolating a cyclic trimer. Additional reaction of ?-diketonates with diethyl zinc were spectroscopically characterized as compounds of the type [{Zn(Et)(?-diketonate)} n ] (?-diketonate=OC(Me)CHC(Me)O, 2, OC(OtBu)CHC(Me)O, 3). Further studies have shown that selective oxidation of these species produces cubanes of the general formula [{Zn(OC(R)CHC(Me)O)2Zn(Et)OEt}2] (R=OMe, 4; Me, 5; OtBu, 6), allowing a high oxygen content whilst remaining structurally suitable for use as precursors. The successful deposition of thin films of zinc oxide through aerosol-assisted chemical vapor deposition (AACVD), using a novel precursor, is described and fully characterized.

SUBMITTER: Manzi JA 

PROVIDER: S-EPMC4981048 | biostudies-literature | 2016 Aug

REPOSITORIES: biostudies-literature

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Synthesis of Trimeric Organozinc Compounds and their Subsequent Reaction with Oxygen.

Manzi Joe A JA   Knapp Caroline E CE   Parkin Ivan P IP   Carmalt Claire J CJ  

ChemistryOpen 20160715 4


A conventional solution-based route to a cyclic trimeric organozinc compound [{Zn(Et)(β-diketonate)}3] (β-diketonate=OC(OMe)CHC(Me)O, 1) is described, with 1 structurally characterized for the first time. The ligand selection of bidentate β-diketonates is shown to be key to isolating a cyclic trimer. Additional reaction of β-diketonates with diethyl zinc were spectroscopically characterized as compounds of the type [{Zn(Et)(β-diketonate)} n ] (β-diketonate=OC(Me)CHC(Me)O, 2, OC(OtBu)CHC(Me)O, 3)  ...[more]

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