4.7 Article

Synthesis of tris(3-pyridyl)aluminate ligand and its unexpected stability against hydrolysis: revealing cooperativity effects in heterobimetallic pyridyl aluminates

Journal

DALTON TRANSACTIONS
Volume 50, Issue 37, Pages 13059-13065

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1dt02351a

Keywords

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Funding

  1. Spanish Ministry of Science, Innovation and Universities (MCIU) [PGC2018-096880-A-I00, PGC2018-099470-B-I00]
  2. European Union (ESF) [RYC-2015-19035]
  3. University of Valladolid
  4. Santander Bank
  5. Spanish MINECO/AEI [RYC-2015-19035]

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The study presents a rare metallic anion [EtAl(3-py)(3)](-) with high protic stability against water and alcohols, unlike related compounds, due to its inability to chelate Li+ and prevent a decomposition pathway involving Li/Al cooperativity.
We report the elusive metallic anion [EtAl(3-py)(3)](-) (3-py = 3-pyridyl) (1), the first member of the anionic tris(3-pyridyl) family. Unexpectedly, the lithium complex 1Li shows substantial protic stability against water and alcohols, unlike related tris(2-pyridyl)aluminate analogues. This stability appears to be related to the inability of the [EtAl(3-py)(3)](-) anion to chelate Li+, which precludes a decomposition pathway involving Li/Al cooperativity.

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