Synthesis, characterization, and reactivity of multinuclear zinc(II) alkylderivatives of linked phenoxides

Citation
Mb. Dinger et Mj. Scott, Synthesis, characterization, and reactivity of multinuclear zinc(II) alkylderivatives of linked phenoxides, INORG CHEM, 40(5), 2001, pp. 1029-1036
Citations number
23
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
INORGANIC CHEMISTRY
ISSN journal
00201669 → ACNP
Volume
40
Issue
5
Year of publication
2001
Pages
1029 - 1036
Database
ISI
SICI code
0020-1669(20010226)40:5<1029:SCAROM>2.0.ZU;2-Z
Abstract
Alkyl zinc derivatives of tris(3,5-dialkyl-2-hydroxyphenyl)methanes (alkyl = tert-butyl la, methyl Ib tert-pentyl Ic) have been prepared by reaction w ith dimethyl or diethylzinc, and characterized Whereas dimethylzinc with la or diethylzinc with Ib give Sg symmetric, hexanuclear aggregates with the general formula 1(2)(ZnR)(6) (R = Me 2a, Et 2b), when la reacts with diethy lzinc, solvent dependent reactions take place. If dichloromethane is used f or the reaction solvent, a dimeric, C-2 symmetric, tetranuclear product wit h the formula 1a(2)Zn(2)(ZnEt)(2) (3) is isolated while in diethyl ether, a Ct symmetric, pentanuclear aggregate 1a(2)Zn(ZnEt)(4) (4) forms, and in te trahydrofuran a C-3 symmetric trinuclear compound la[ZnEt(THF)](3) (5a) is produced. Each example is represented by a single-crystal X-ray structure d etermination. Preliminary studies regarding their activity toward the copol ymerization of cyclohexene oxide and carbon dioxide are also reported.