6-Cyclophane)(η6-benzene)ruthenium(II) bis(tetrafluoroborate) complexes and their geometry-dependent 13C NMR behavior

Toshihide Miura, Tomoyo Horishita, Nobuo Mori

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)


Transition-metal complexation effects which can be observed in 13C NMR spectra have been investigated for the (η6-cyclophane)(η6-benzene)ruthenium(II) bis(tetrafluoroborate) complexes, where the cyclophane moiety is [8]-[15]paracyclophane, [2.2]paracyclophane, [2.2]metacyclophane or 5,13-dimethyl[2.2]metacyclophane. The complexation shifts for the complexed cyclophane-ring carbons are dependent on the degree and direction of ring bending. The magnitude of the complexation effect on the one-bond aromatic 13C1H coupling correlates with the magnitude of the complexation shift.

Original languageEnglish
Pages (from-to)387-392
Number of pages6
JournalJournal of Organometallic Chemistry
Issue number3
Publication statusPublished - 1987 Oct 27
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry
  • Materials Chemistry


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