4.6 Article

Helicate extension as a route to molecular wires

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 14, 期 24, 页码 7180-7185

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.200800503

关键词

conducting materials; coordination chemistry; dynamic covalent chemistry; self-assembly

资金

  1. Walters-Kundert Charitable Trust
  2. Swiss State Secretariat for Education and Research
  3. Swiss National Science Foundation [20EC21-112706, PP002-114828 200020-120007]
  4. US National Science Foundation [CHE-0610183]
  5. Academy of Finland [122350]

向作者/读者索取更多资源

We describe the preparation of a helicate containing four closely spaced, linearly arrayed copper(I) ions. This product may be prepared either directly by mixing copper(I) with a set of precursor amine and aldehyde subcomponents, or indirectly through the dimerization of a dicopper(I) helicate upon addition of 1,2-phenylenediamine. A notable feature of this helicate is that its length is not limited by the lengths of its precursor subcomponents: each of the two ligands wrapped around the four copper(I) centers contains one diamine, two dialdehyde, and two monoamine residues. This work thus paves the way for the preparation of longer oligo- and polymeric structures. DFT calculations and electrochemical measurements indicate a high degree of electronic delocalization among the metal ions forming the cores of the structures described herein, which may therefore be described as molecular wires.

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