Abstract
Two sterically congested lithium 1-(2',6'-di-tert-butylphenyl)alken-1-olates, LiO-C(=CHR)-aryl, were observed exclusively either as threefold THF-microsolvated, cisoid dimers or as donor-free aggregates. Each one of the two dimmers carries one quasi-tetrahedral and one trigonally planar Li center whose properties interconvert through fast THF transposition along two pathways. The trigonally planar Li cation, microsolvated by only one THF ligand, is heavily shielded by all four tert-butyl groups in the dimer. Roughly estimated reactivities against some electrophilic reagents varied between fast and extremely slow for both the THF-microsolvated and the donor-free forms. (C) 2021 Elsevier Ltd. All rights reserved.
Item Type: | Journal article |
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Faculties: | Chemistry and Pharmacy > Department of Chemistry |
Subjects: | 500 Science > 540 Chemistry |
ISSN: | 0040-4020 |
Language: | English |
Item ID: | 99636 |
Date Deposited: | 05. Jun 2023 15:32 |
Last Modified: | 05. Jun 2023 15:32 |