Silapillar[n]arenes: Their Enhanced Electronic Conjugation and Conformational Versatility.
J Am Chem Soc
; 146(7): 4695-4703, 2024 Feb 21.
Article
in En
| MEDLINE
| ID: mdl-38324921
ABSTRACT
During recent decades, methylene-bridged macrocyclic arenes have been widely used in supramolecular chemistry. However, their π-conjugations are very weak, as the methylene bridges disrupt the electronic communication between π orbitals of the aromatic units. Herein, we successfully synthesized a series of silapillar[n]arenes (n = 4, 6, and 8) using silylene bridging. These showed enhanced electronic conjugation compared with the parent pillar[n]arenes because of σ*-π* conjugation between σ* (Si-C) orbitals and π* orbitals of the benzenes. Owing to the longer Si-C bond compared with the C-C bond, silylene-bridging provides additional structural flexibility into the pillar[n]arene scaffolds; a strained silapillar[4]arene was formed, which is unavailable in the parent pillar[n]arenes because of the steric requirements. Furthermore, silapillar[n]arenes displayed interesting size-dependent structural and optical properties.
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01-internacional
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MEDLINE
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En
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J Am Chem Soc
Year:
2024
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Article
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