Abstract
To further our understanding of the coordination chemistry of the heavy alkaline earth metals, we here report on a family of barium pyrazolates bearing various substitution patterns that illustrate the delicate balance between ligand bulk, donor size, stoichiometry, and hapticity, while emphasizing the importance of secondary interactions including π-bonding, agostic interactions, and hydrogen bonding to stabilize these heavy-metal complexes. The dimeric compounds [{Ba(Me2pz)2(pmdta)}2] (1), [{Ba(Phpz)2(pmdta)}2] (2), [{Ba(tBupz)2(pmdta)} 2] (3), [{Ba(MePhpz)2(tmeda)}2] (5), [{Ba(Ph2pz)2(tmeda)}2]·TMEDA (6), the polymer [{Ba(tBupz)2(NH3)2}n] (4), and the monomer [Ba(Ph2pz)2(tmeda)2] ·TMEDA (7), were prepared using a variety of synthetic methods and were characterized spectroscopically and structurally.
Original language | English |
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Pages (from-to) | 172-182 |
Number of pages | 11 |
Journal | European Journal of Inorganic Chemistry |
Issue number | 1 |
DOIs | |
Publication status | Published - 2008 |
Keywords
- Barium
- Coordination modes
- CVD precursors
- N ligands
- Pyrazolates
- Structure elucidation
- Synthetic methods
ASJC Scopus subject areas
- Inorganic Chemistry