The first osmium(II), ruthenium(II) and iron(II) complexes of [3n]cyclophanes (n = 2-4): Synthesis and electrochemical study

Teizi Satou, Ko Takehara, Mihoko Hirakida, Youichi Sakamoto, Hiroyuki Takemura, Hirokazu Miura, Mie Tomonou, Teruo Shinmyozu

研究成果: Contribution to journalArticle査読

16 被引用数 (Scopus)

抄録

6-C6H6)(η6-[3 n]Cyclophane)Ru(II) [BF4]2 and corresponding Os(II) [PF6]2, as well as bis(η5-C5H5)(η66-[3n]cyclophane)Fe(II)Fe(II) [PF6]2 ([3n]cyclophane = [32](1,4)cyclophane 2, [33](1,3,5)cyclophane 3, [34](1,2,3,5)cyclophane 4, [34](1,2,4,5)cyclophane 5) have been synthesized and characterized. The complexation shifts of the 1H-NMR signals of the metal-bound aromatic protons (Hb) are ca. 0.5-0.7 and 0.1-0.4 ppm for Fe(II) and Ru(II) complexes, respectively, whereas those of Os(II) complexes are ca. -0.2-0.1 ppm. The complexation shifts of the 13C-NMR signals of the tertiary aromatic carbons of the metal-bound benzene ring are ca. 39-42 and 45-50 ppm for Ru(II) and Os(II) complexes, respectively. Thus the 1H- and 13C-NMR chemical shifts of the metal-bound aromatic hydrogens and carbons are strongly influenced by the anisotropy effect of the metal. The Ru(II) complexes showed electrochemically reversible responses. In the case of Os(II) complexes, a well-defined cathodic peak was also observed, but the rising portion of the corresponding anodic peak was somewhat deviated from the ordinary CV profile. In both cases, the redox process was attributed to the two-electron one-step mechanism, M(II) ⇌ M(0) (M = Ru and Os). An analysis of the redox properties of the Ru(II) and Os(II) complexes suggested that the Os(II)[34](1,2,4,5)cyclophane complex would be the most suitable subunit of an anticipated one-dimensional organometallic polymer.

本文言語英語
ページ(範囲)58-68
ページ数11
ジャーナルJournal of Organometallic Chemistry
577
1
DOI
出版ステータス出版済み - 3 27 1999

All Science Journal Classification (ASJC) codes

  • 生化学
  • 物理化学および理論化学
  • 有機化学
  • 無機化学
  • 材料化学

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