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• W4381716213 abstract "The peripheral borylation of porphyrinoids has become a key step to prepare advanced functional materials. This study reports the synthesis, electronic properties, and reactivity of borylated subphthalocyanines. These compounds, which are prepared by Suzuki-Miyaura borylation in excellent yields, are easily purified, display a great stability, and serve as powerful starting materials for the post-functionalization of SubPcs via cross-coupling reactions. Remarkably, this novel approach is more efficient than the methodologies already described and enables the preparation of exotic systems, such as SubPc dimeric species linked by C-C bonds, which are not accessible so far and present promising properties for optoelectronic devices." @default.
• W4381716213 created "2023-06-24" @default.
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• W4381716213 date "2023-08-08" @default.
• W4381716213 modified "2023-09-23" @default.
• W4381716213 title "Borylated Subphthalocyanines: Versatile Precursors for the Preparation of Functional Bowl‐Shaped Aromatics" @default.
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• W4381716213 doi "https://doi.org/10.1002/chem.202301782" @default.
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