Germylene Mediated Reductive C-C and C‒N Coupling of an Isocyanide and its Device Application

We have demonstrated a unique reductive coupling of 4-iodophenyl isocyanide, facilitated by a perimidine-based N-heterocyclic germylene (NHGe), which yields a bis-spirogerma compound featuring simultaneous C‒C and C‒N bond formation. This reaction, which leads to the oxidation of germanium from +2 t...

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Veröffentlicht in:Angewandte Chemie International Edition 2024-11, p.e202417052
Hauptverfasser: Gour, Kritika, Pramanik, Debjit, Dash, Soumya, Shinde, Dipak, Venugopal, Geethu, Vanka, Kumar, Rath, Arup, Sen, Sakya S
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Sprache:eng
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Zusammenfassung:We have demonstrated a unique reductive coupling of 4-iodophenyl isocyanide, facilitated by a perimidine-based N-heterocyclic germylene (NHGe), which yields a bis-spirogerma compound featuring simultaneous C‒C and C‒N bond formation. This reaction, which leads to the oxidation of germanium from +2 to +4, represents a significant departure from previously documented isocyanide-germylene interactions. The product exhibits extensive conjugation across its bicyclic C₄Ge₂N₂ framework, conferring distinct photophysical properties, including prominent orange luminescence in both solution and solid states. The photophysical properties are supported by the TD-DFT calculations confirming an n→π* transition. The potential application of this compound in optoelectronic devices, particularly as a hole transport layer in PbS quantum dot solar cells, is also explored, with promising preliminary results.
ISSN:1433-7851
1521-3773
1521-3773
DOI:10.1002/anie.202417052