Tuneable intramolecular intermetallic interactions as a new tool for programming linear heterometallic 4f-4f complexes

Statistical mechanics predicts that the design of pure organized heteropolymetallic chains of metal ions bound to linear receptors depends on controlled deviations from the mixing rule DeltaE(MiMj) = 1/2 (DeltaE(MiMi) + DeltaE(MjMj)), whereby DeltaE(MiMj) is the intramolecular intermetallic interact...

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Vydané v:Inorganic chemistry Ročník 46; číslo 22; s. 9312
Hlavní autori: Dalla-Favera, Natalia, Hamacek, Josef, Borkovec, Michal, Jeannerat, Damien, Ercolani, Gianfranco, Piguet, Claude
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States 29.10.2007
ISSN:0020-1669
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Shrnutí:Statistical mechanics predicts that the design of pure organized heteropolymetallic chains of metal ions bound to linear receptors depends on controlled deviations from the mixing rule DeltaE(MiMj) = 1/2 (DeltaE(MiMi) + DeltaE(MjMj)), whereby DeltaE(MiMj) is the intramolecular intermetallic interaction between neighboring metal i and metal j along the receptor. A thorough investigation of linear polymetallic trivalent lanthanide triple-stranded helicates shows that such deviations are amplified by an increase in the nuclearity of the final complexes and are thus easily evidenced in the tetranuclear heterobimetallic helicates [La(4-y)Lu(y)(L6)3](12+) (y = 0-4). The chemical and physical origins of this unprecedented behavior are discussed together with its practical consequences for programming pure heteropolymetallic 4f-4f complexes.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:0020-1669
DOI:10.1021/ic701308h