Surface-Confined Macrocyclization via Dynamic Covalent Chemistry

0522609 - ÚFCH JH 2021 RIV US eng J - Článek v odborném periodiku
Fu, Ch. - Mikšátko, Jiří - Assies, Lea - Vrkoslav, Vladimír - Orlandini, S. - Kalbáč, Martin - Kovaříček, Petr - Zeng, X. - Zhou, B. - Muccioli, L. - Perepichka, D.F. - Orgiu, E.
Surface-Confined Macrocyclization via Dynamic Covalent Chemistry.
ACS Nano. Roč. 14, č. 3 (2020), s. 2956-2965. ISSN 1936-0851. E-ISSN 1936-086X
Grant CEP: GA ČR GA18-20357S; GA MŠMT(CZ) LM2015073; GA MŠMT(CZ) EF16_013/0001821
Institucionální podpora: RVO:61388955 ; RVO:61388963
Klíčová slova: dynamic covalent chemistry * on-surface synthesis * macrocycle
Obor OECD: Physical chemistry; Analytical chemistry (UOCHB-X)
Impakt faktor: 15.881, rok: 2020
Způsob publikování: Omezený přístup

Surface-confined synthesis is a promising approach to build complex molecular nanostructures including macrocycles. However, despite the recent advances in on-surface macrocyclization under ultrahigh vacuum, selective synthesis of monodisperse and multicomponent macrocycles remains a challenge. Here, we report on an on-surface formation of [6 + 6] Schiff-base macrocycles via dynamic covalent chemistry. The macrocycles form two-dimensional crystalline domains on the micrometer scale, enabled by dynamic conversion of open-chain oligomers into well-defined ∼3.0 nm hexagonal macrocycles. We further show that by tailoring the length of the alkyl substituents, it is possible to control which of three possible products-oligomers, macrocycles, or polymers-will form at the surface. In situ scanning tunneling microscopy imaging combined with density functional theory calculations and molecular dynamics simulations unravel the synergistic effect of surface confinement and solvent in leading to preferential on-surface macrocyclization.
Trvalý link: http://hdl.handle.net/11104/0307074