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Programming heterometallic 4f-4f' helicates under thermodynamic control: the circle is complete.
Egger, Charlotte; Guénée, Laure; Deorukhkar, Neel; Piguet, Claude.
Afiliação
  • Egger C; Department of Inorganic and Analytical Chemistry, University of Geneva, 30 quai E. Ansermet, CH-1211 Geneva 4, Switzerland. Claude.Piguet@unige.ch.
  • Guénée L; Laboratory of Crystallography, University of Geneva, 24 quai E. Ansermet, CH-1211 Geneva 4, Switzerland.
  • Deorukhkar N; Department of Inorganic and Analytical Chemistry, University of Geneva, 30 quai E. Ansermet, CH-1211 Geneva 4, Switzerland. Claude.Piguet@unige.ch.
  • Piguet C; Department of Inorganic and Analytical Chemistry, University of Geneva, 30 quai E. Ansermet, CH-1211 Geneva 4, Switzerland. Claude.Piguet@unige.ch.
Dalton Trans ; 53(13): 6050-6062, 2024 Mar 26.
Article em En | MEDLINE | ID: mdl-38470853
ABSTRACT
Three non-symmetrical segmental ligand strands L4 can be wrapped around a linear sequence of one Zn2+ and two trivalent lanthanide cations Ln3+ to give quantitatively directional [ZnLn2(L4)3]8+ triple-stranded helicates in the solid state and in solution. NMR speciations in CD3CN show negligible decomplexation at a millimolar concentration and the latter helicate can be thus safely considered as a preorganized C3-symmetrical HHH-[(L43Zn)(LnA)(2-n)(LnB)n]8+ platform in which the thermodynamic properties of (i) lanthanide permutation between the central N9 and the terminal N6O3 binding sites and (ii) exchange processes between homo- and heterolanthanide helicates are easy to access (Ln = La, Eu, Lu). Deviations from statistical distributions could be programmed by exploiting specific site recognition and intermetallic pair interactions. Considering the challenging La3+ Eu3+ ionic pair, for which the sizes of the two cations differ by only 8%, a remarkable excess (70%) of the heterolanthanide is produced, together with a preference for the formation of the isomer where the largest lanthanum cation lies in the central N9 site ([(La)(Eu)] [(Eu)(La)] = 9 1). This rare design and its rational programming pave the way for the preparation of directional light-converters and/or molecular Q-bits at the (supra)molecular level.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Dalton Trans Assunto da revista: QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Suíça País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Dalton Trans Assunto da revista: QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Suíça País de publicação: Reino Unido