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Formation and Reactivity of an Aluminabenzene Ligand at Pentadienyl‐Supported Rare‐Earth Metals
Author(s) -
Barisic Damir,
Schneider David,
MaichleMössmer Cäcilia,
Anwander Reiner
Publication year - 2019
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201812515
Subject(s) - yttrium , reactivity (psychology) , chemistry , acetylide , metathesis , rare earth , ligand (biochemistry) , medicinal chemistry , salt metathesis reaction , metal , salt (chemistry) , crystallography , stereochemistry , polymerization , oxide , organic chemistry , mineralogy , medicine , biochemistry , polymer , alternative medicine , receptor , pathology
The half‐open rare‐earth‐metal aluminabenzene complexes [(1‐Me‐3,5‐ t Bu 2 ‐C 5 H 3 Al)(μ‐Me)Ln(2,4‐dtbp)] (Ln=Y, Lu) are accessible via a salt metathesis reaction employing Ln(AlMe 4 ) 3 and K(2,4‐dtbp). Treatment of the yttrium complex with B(C 6 F 5 ) 3 and t BuCCH gives access to the pentafluorophenylalane complex [{1‐(C 6 F 5 )‐3,5‐ t Bu 2 ‐C 5 H 3 Al}{μ‐C 6 F 5 }Y{2,4‐dtbp}] and the mixed vinyl acetylide complex [(2,4‐dtbp)Y(μ‐η 1 :η 3 ‐2,4‐ t Bu 2 ‐C 5 H 4 )(μ‐CC t Bu)AlMe 2 ], respectively.
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