2018
DOI: 10.1039/c8ra01819g
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Extension and functionalization of an encapsulating macrobicyclic ligand using palladium-catalyzed Suzuki–Miyaura and Sonogashira reactions of iron(ii) dihalogenoclathrochelates with inherent halogen substituents

Abstract: A new approach for performing Suzuki and Sonogashira reactions of iron(ii) dihalogenoclathrochelates, optimizing their reaction conditions, is elaborated.

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Cited by 6 publications
(2 citation statements)
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“…The inert character of boron-capped clathrochelates offers the opportunity to perform postsynthetic modifications. For example, clathrochelates can be used in palladium-catalyzed cross-coupling reactions (Scheme , top). For modifications in lateral position, substitution reactions are an interesting option. It is possible to prepare clathrochelate complexes containing between one and six chloro atoms in lateral position.…”
Section: Introductionmentioning
confidence: 99%
“…The inert character of boron-capped clathrochelates offers the opportunity to perform postsynthetic modifications. For example, clathrochelates can be used in palladium-catalyzed cross-coupling reactions (Scheme , top). For modifications in lateral position, substitution reactions are an interesting option. It is possible to prepare clathrochelate complexes containing between one and six chloro atoms in lateral position.…”
Section: Introductionmentioning
confidence: 99%
“…[26][27][28] Iron(II) clathrochelate is a robust metalorganic unit with a considerable internal free volume (IFV) and which can be easily synthesized and functionalized, especially when employed as a building block in cross-coupling reactions. [29][30][31] Iron(II) clathrochelate complexes were tested as biosensors, 32,33 catalysts for hydrogen generation, 34,35 materials for electronic transport, 36 organogels, 37 and to make supramolecular structures of denite shapes and sizes. [38][39][40][41] Recently, several iron(II) clathrochelate based polymers were reported disclosing prominent porous properties.…”
Section: Introductionmentioning
confidence: 99%