Structural Diversity of Heteroleptic 1,2,4-Triphenylcyclopentadienyl-Bipyridine Complexes of Rare Earth Metals

The reaction of triphenylcyclopentadienyl potassium and bipyridine with lanthanum, praseodymium, erbium, lutetium, and scandium chloride tetrahydrofuranates results in the formation of binuclear [Cp Ph3 Ln(Bipy)Cl(μ 2 -Cl)] 2 (Ln = La ( I ), Pr ( II )) and mononuclear [Cp Ph3 Ln(Bipy)Cl 2 (THF)] (Ln...

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Veröffentlicht in:Russian journal of coordination chemistry 2024-05, Vol.50 (5), p.334-342
Hauptverfasser: Bardonov, D. A., Lyssenko, K. A., Degtyareva, S. S., Nifant’ev, I. E., Roitershtein, D. M.
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container_end_page 342
container_issue 5
container_start_page 334
container_title Russian journal of coordination chemistry
container_volume 50
creator Bardonov, D. A.
Lyssenko, K. A.
Degtyareva, S. S.
Nifant’ev, I. E.
Roitershtein, D. M.
description The reaction of triphenylcyclopentadienyl potassium and bipyridine with lanthanum, praseodymium, erbium, lutetium, and scandium chloride tetrahydrofuranates results in the formation of binuclear [Cp Ph3 Ln(Bipy)Cl(μ 2 -Cl)] 2 (Ln = La ( I ), Pr ( II )) and mononuclear [Cp Ph3 Ln(Bipy)Cl 2 (THF)] (Ln = Er ( III ), Lu ( IV ), [Cp Ph3 Sc(Bipy)Cl 2 ] ( V ) complexes (Cp Ph3 = 1,2,4-triphenylcyclopentadienyl, Bipy = bipyridine). The decrease in the REE radius in the series La…Sc results in the formation of mononuclear instead of binuclear complexes and in a decrease in the coordination number of the central ion. The coplanar arrangement of two different π-systems gives rise to stacking interactions between the triphenylcyclopentadienyl ligand and bipyridine. The molecular structure of complexes I – V was established by X-ray diffraction analysis (CCDC nos. 2308609 ( I ), 2308608 ( II ), 2308610 ( III ), 2308611 ( IV ), 2308607 ( V )).
doi_str_mv 10.1134/S1070328423601565
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The coplanar arrangement of two different π-systems gives rise to stacking interactions between the triphenylcyclopentadienyl ligand and bipyridine. 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The decrease in the REE radius in the series La…Sc results in the formation of mononuclear instead of binuclear complexes and in a decrease in the coordination number of the central ion. The coplanar arrangement of two different π-systems gives rise to stacking interactions between the triphenylcyclopentadienyl ligand and bipyridine. The molecular structure of complexes I – V was established by X-ray diffraction analysis (CCDC nos. 2308609 ( I ), 2308608 ( II ), 2308610 ( III ), 2308611 ( IV ), 2308607 ( V )).</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1070328423601565</doi><tpages>9</tpages></addata></record>
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subjects Chemistry
Chemistry and Materials Science
Coordination numbers
Erbium
Inorganic Chemistry
Lanthanum
Lutetium
Molecular structure
Physical Chemistry
Praseodymium
Rare earth elements
Scandium
title Structural Diversity of Heteroleptic 1,2,4-Triphenylcyclopentadienyl-Bipyridine Complexes of Rare Earth Metals
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