GeCl<sub>2</sub>‑MediatedRing Contractiontoward Endofullerenes

Germanium­(II) dichloride dioxane complex (GeCl<sub>2</sub>·dioxane) is often utilized as a source of molecular germylene, i.e., GeCl<sub>2</sub>, which is known to undergo oxidative 1,4-addition to conjugated substrates. Inspired by this nature resembled to carbenes, we demonstrated a CC bond formation from two carbonyl moieties engaged in an aromatic macrocycle. This germylene-mediated reaction enables us to realize efficient synthesis of endo[60]­fullerenes through the consecutive ring contraction of open-[60]­fullerenes.

Publication Details

Journal
Figshare
Published
2025-03-26
DOI
https://doi.org/10.1021/acs.joc.5c00217.s001
Primary Topic
Fullerene Chemistry and Applications
Type
article
Field-Weighted Citation Impact
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GeCl2‑MediatedRing Contractiontoward Endofullerenes

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Fullerene Chemistry and Applications
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GeCl2‑MediatedRing Contractiontoward Endofullerenes

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Abstract

Germanium­(II) dichloride dioxane complex (GeCl<sub>2</sub>·dioxane) is often utilized as a source of molecular germylene, i.e., GeCl<sub>2</sub>, which is known to undergo oxidative 1,4-addition to conjugated substrates. Inspired by this nature resembled to carbenes, we demonstrated a CC bond formation from two carbonyl moieties engaged in an aromatic macrocycle. This germylene-mediated reaction enables us to realize efficient synthesis of endo[60]­fullerenes through the consecutive ring contraction of open-[60]­fullerenes.

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Openalex Percentile: Top 69%
Fullerene Chemistry and Applications
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GeCl<sub>2</sub>‑MediatedRing Contractiontoward Endofullerenes · Figshare (2025) | TGRS Research Map | TGRS