A Disila[2]ferrocenophane with a Bridging 9,9′-Bi-9H-9-Silafluorene Moiety

A disila[2]ferrocenophane bearing a 9,9'-bi-9<i>H</i>-9-silafluorene (9-silafluorene dimer) moiety as a bridging unit was synthesized and isolated as a stable crystalline compound. Disila[2]ferrocenophane <b>1,</b> newly obtained in this study, has been characterized by spectroscopic analyses, single crystal X-ray diffraction (SC-XRD) analysis, and electrochemical measurements. It was found that the obtained disila[2]ferrocenophane was reduced by a reducing agent to generate the corresponding 1,1'-ferrocenediyl-bis(silylanion) via the reductive Si-Si σ-bond cleavage. The trapping reactions of the 1,1'-ferrocenediyl-bis(silylanion) thus generated with electrophiles have also been attempted.

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Publication Details

Journal
Molecules
Published
2025-03-18
DOI
https://doi.org/10.3390/molecules30061361
Citations
1
Primary Topic
Synthesis and characterization of novel inorganic/organometallic compounds
Type
article
Field-Weighted Citation Impact
0.54

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article

A Disila[2]ferrocenophane with a Bridging 9,9′-Bi-9H-9-Silafluorene Moiety

Koh Sugamata, Koichiro Masada, Shogo Morisako, Takahiro Sasamori et al.
1 citations
Molecules
Synthesis and characterization of novel inorganic/organometallic compounds
0.54
article

A Disila[2]ferrocenophane with a Bridging 9,9′-Bi-9H-9-Silafluorene Moiety

Koh Sugamata, Koichiro Masada, Shogo Morisako, Takahiro Sasamori, Shinnosuke Usuba
article en
1 citations

Abstract

A disila[2]ferrocenophane bearing a 9,9'-bi-9<i>H</i>-9-silafluorene (9-silafluorene dimer) moiety as a bridging unit was synthesized and isolated as a stable crystalline compound. Disila[2]ferrocenophane <b>1,</b> newly obtained in this study, has been characterized by spectroscopic analyses, single crystal X-ray diffraction (SC-XRD) analysis, and electrochemical measurements. It was found that the obtained disila[2]ferrocenophane was reduced by a reducing agent to generate the corresponding 1,1'-ferrocenediyl-bis(silylanion) via the reductive Si-Si σ-bond cleavage. The trapping reactions of the 1,1'-ferrocenediyl-bis(silylanion) thus generated with electrophiles have also been attempted.

MoleculesVol. 30(6)
University of Tsukuba (JP), Sagami Chemical Research Institute (JP)
Japan Society for the Promotion of Science
Clean water and sanitation
Openalex Percentile: Top 38%
Synthesis and characterization of novel inorganic/organometallic compounds
0.54
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A Disila[2]ferrocenophane with a Bridging 9,9′-Bi-9H-9-Silafluorene Moiety — Koh Sugamata, Koichiro Masada, et al. · Molecules (2025) | TGRS Research Map | TGRS