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Lanthanide cyclooctatetraene dianion

Controversy exists in naming sandwich organometallic actinide and lanthanide compounds of cyclooctatetraene dianion [8]annulene dianion and [8]annulene-metal(X) complex are chosen here because these names properly describe the delocalization of charge in the ligand and also emphasize the formal oxidation state of the metal in the complex. [Pg.109]

Uranocene (15.19), a key discovery from 1%8, showed that the higher radius and charge of relative to the lanthanides allows stabilization of the planar, aromatic, lOrr-electron cyclooctatetraene dianion (cot ) in U(cot)2. This pyrophoric 22e compound also shows the failure of the 18e rule in the 5/ elements. [Pg.486]

The bis([8]annulene)lanthanate(III) anions which are complexed by an [8]annulenelanthanate(III) cation are the only other class of complexes which contain two [8]annulene dianions in a sandwich arrangement about a lanthanide(III) ion. This class was first reported for the cerium(III) ion, from the reduction of a cerium(IV) alkoxide with triethylaluminum in the presence of cyclooctatetraene.3 ... [Pg.88]

Cyclooctatetraene CgHg (COT) can be an 8-electron L4 ligand. With the alkaline metals, lanthanides and actinides however, COT is found as the aromatic COT dianion with 10 electrons (Hiickel s rule 4n -1- 2n electrons, n = 2). [Pg.30]


See other pages where Lanthanide cyclooctatetraene dianion is mentioned: [Pg.24]    [Pg.63]    [Pg.29]    [Pg.32]    [Pg.407]    [Pg.366]   


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