Тип публикации: статья из журнала
Год издания: 2022
Идентификатор DOI: 10.1002/anie.202208247
Аннотация: <jats:title>Abstract</jats:title><jats:p>Under cold pressure sp<jats:sup>1</jats:sup>/sp<jats:sup>2</jats:sup>-to-sp<jats:sup>3</jats:sup> hybridization transformation has been exclusively observed in covalent or molecular crystals overwhelmingly above ≈10 GPa, and the approaches to lower the transition pressure are limited on exteПоказать полностьюrnal heat-treatment and/or catalyzers. Herein we demonstrate that, by internal-lattice stress-transfer from ionic to covalent groups, the transformation can be significantly prompted, as shown in a crystal of LiBO<jats:sub>2</jats:sub> under 2.85 GPa for the first case in ionic crystals. This unprecedentedly low transformation pressure is ascribed to the enhanced localized stress on covalent B−O frames transferred from ionic Li−O bonds in LiBO<jats:sub>2</jats:sub>, and accordingly the corresponding structural feature is summarized. This work provides an internal structural regulation strategy for pressure-reduction of the s-p orbital hybridization transformation and extends the sp<jats:sup>1</jats:sup>/sp<jats:sup>2</jats:sup>-to-sp<jats:sup>3</jats:sup> transformation landscape from molecular and covalent compounds to ionic systems.</jats:p>
Журнал: Angewandte Chemie International Edition
Выпуск журнала: Т. 61, № 44
ISSN журнала: 14337851
Издатель: Wiley Interscience