Pyrolysis conversion of crown-ether-based covalent networks to kagome metal-organic frameworks on Au(111) and Ag(111)

• The 24-crown-8 ether displays a distinct “8”-shaped ring structure. • Four and six-membered rings formed during dimerization and trimerization. • The crown ether undergoes dehydrogenation on Ag(111) annealed at 520 k. • Pyrolysis of crown ethers leads to a long-range ordered triphenylene-based MOF. • The MOF structure on Ag(111) hosts both kagome lattices and quantum dot-like states. On-surface chemistry provides an efficient approach to construction of diverse covalent architectures with atomic precision, ranging from one-dimensional chains and ribbons to two-dimensional covalent organic frameworks (COFs) and metal-organic frameworks (MOFs) on coinage metal substrates. This study explores a distinct on-surface pyrolysis approach to MOFs derived from a crown ether molecular precursor on Au(111) and Ag(111) surfaces. Utilizing scanning tunneling microscopy (STM) and non-contact atomic force microscopy (nc-AFM) combined with density functional theory (DFT) calculations, we elucidate the adsorption behavior and the characteristic macrocyclic configuration of the crown ether on Au(111). Subsequent surface-catalyzed Ullmann coupling reactions at an annealing temperature of 470 K lead to highly disordered COFs with the formation of four-membered and six-membered rings through dimerization and trimerization. For the Ag(111) surface, further annealing at 520 K initiates a unique dehydrogenative reaction within the macrocyclic rings, resulting in the loss of six hydrogen atoms. At an elevated temperature of 720 K, breaking of the second C−O bonds yields a long-range ordered triphenylene-based MOF structure. Electronic characterizations reveal the presence of both regular and diatomic kagome lattices, together with distinct quantum-dot states emerging in the pore regions. Additionally, we investigate the selective encapsulation of single guest picenes within the MOF structure, emphasizing the potential of triphenylene-based frameworks for advanced applications in sensing and molecular filtering. Our findings provide a comprehensive insight into the chemical reactivity of crown ethers on metal substrates and demonstrate a novel pathway to designing MOFs through an on-surface pyrolysis process.

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Publication Details

Journal
Carbon Trends
Published
2025-01-27
DOI
https://doi.org/10.1016/j.cartre.2025.100474
Citations
3
Primary Topic
Surface Chemistry and Catalysis
Type
article
Field-Weighted Citation Impact
2.02

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article

Pyrolysis conversion of crown-ether-based covalent networks to kagome metal-organic frameworks on Au(111) and Ag(111)

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3 citations
Carbon Trends
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2.02
article

Pyrolysis conversion of crown-ether-based covalent networks to kagome metal-organic frameworks on Au(111) and Ag(111)

Yifan Liang, Shijing Tan, Ruoting Yin, Chuanxu Ma, Qunxiang Li, Jie Meng, Zhengya Wang, Jianing Wang, Bing Wang, Xiaoqing Wang
article en
3 citations

Abstract

• The 24-crown-8 ether displays a distinct “8”-shaped ring structure. • Four and six-membered rings formed during dimerization and trimerization. • The crown ether undergoes dehydrogenation on Ag(111) annealed at 520 k. • Pyrolysis of crown ethers leads to a long-range ordered triphenylene-based MOF. • The MOF structure on Ag(111) hosts both kagome lattices and quantum dot-like states. On-surface chemistry provides an efficient approach to construction of diverse covalent architectures with atomic precision, ranging from one-dimensional chains and ribbons to two-dimensional covalent organic frameworks (COFs) and metal-organic frameworks (MOFs) on coinage metal substrates. This study explores a distinct on-surface pyrolysis approach to MOFs derived from a crown ether molecular precursor on Au(111) and Ag(111) surfaces. Utilizing scanning tunneling microscopy (STM) and non-contact atomic force microscopy (nc-AFM) combined with density functional theory (DFT) calculations, we elucidate the adsorption behavior and the characteristic macrocyclic configuration of the crown ether on Au(111). Subsequent surface-catalyzed Ullmann coupling reactions at an annealing temperature of 470 K lead to highly disordered COFs with the formation of four-membered and six-membered rings through dimerization and trimerization. For the Ag(111) surface, further annealing at 520 K initiates a unique dehydrogenative reaction within the macrocyclic rings, resulting in the loss of six hydrogen atoms. At an elevated temperature of 720 K, breaking of the second C−O bonds yields a long-range ordered triphenylene-based MOF structure. Electronic characterizations reveal the presence of both regular and diatomic kagome lattices, together with distinct quantum-dot states emerging in the pore regions. Additionally, we investigate the selective encapsulation of single guest picenes within the MOF structure, emphasizing the potential of triphenylene-based frameworks for advanced applications in sensing and molecular filtering. Our findings provide a comprehensive insight into the chemical reactivity of crown ethers on metal substrates and demonstrate a novel pathway to designing MOFs through an on-surface pyrolysis process.

Carbon TrendsVol. 19
University of Science and Technology of China (CN), Quantum Design (Germany) (DE)
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 16%
Surface Chemistry and Catalysis
2.02
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