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<dc:title>Synthesis of tris(3-pyridyl)aluminate ligand and its unexpected stability against hydrolysis: revealing cooperativity effects in heterobimetallic pyridyl aluminates</dc:title>
<dc:creator>García Romero, Álvaro</dc:creator>
<dc:creator>Martín Álvarez, José Miguel</dc:creator>
<dc:creator>Colebatch, Annie Louise</dc:creator>
<dc:creator>Plajer, Alex J.</dc:creator>
<dc:creator>Miguel San José, Daniel</dc:creator>
<dc:creator>Álvarez González, Celedonio Manuel</dc:creator>
<dc:creator>García Rodríguez, Raúl</dc:creator>
<dc:description>Producción Científica</dc:description>
<dc:description>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.</dc:description>
<dc:date>2021-10-25T12:29:51Z</dc:date>
<dc:date>2021-10-25T12:29:51Z</dc:date>
<dc:date>2021</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>Dalton Transactions, 2021, vol. 50, n. 37. p. 13059-13065</dc:identifier>
<dc:identifier>1477-9234</dc:identifier>
<dc:identifier>https://uvadoc.uva.es/handle/10324/49357</dc:identifier>
<dc:identifier>10.1039/D1DT02351A</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>https://pubs.rsc.org/en/content/articlelanding/2021/DT/D1DT02351A</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>© 2021 Royal Society of Chemistry</dc:rights>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
<dc:publisher>Royal Society of Chemistry</dc:publisher>
<dc:peerreviewed>SI</dc:peerreviewed>
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