Conjugated Nanobelts Based on <i>N</i> -Hetero[(6.) <sub> <i>m</i> </sub> 8] <sub> <i>n</i> </sub> cyclacene

<span>This study introduces a novel design of </span><i>N</i><span>-doped conjugated nanobelts, derived from a specific structural unit found in carbon schwarzites, a type of negatively curved carbon allotrope. The successful synthesis of these nanobelts was achieved using a flexible curved building block in a condensation reaction with </span><i>ortho</i><span>-quinones. The electronic structure and aromaticity of the diazatetracene-based nanobelt were investigated and compared with diazatetracene dimers through a combination of computational and experimental methods, revealing the influence of macrocyclization on these attributes. Notably, the diazatetracene-based nanobelt encapsulates C</span><span>70</span><span> in toluene with a high binding constant of (2.8 ± 0.2) × 10</span><span>5</span><span> M</span><span>−1</span><span>, demonstrating significant selectivity against C</span><span>60</span><span>. X-ray crystallographic analysis indicated that the nanobelt adjusts its rhombus cross section to enhance host–guest interactions when accommodating C</span><span>70</span><span>.</span>

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Publication Details

Journal
CCS Chemistry
Published
2024-12-20
DOI
https://doi.org/10.31635/ccschem.024.202405108
Citations
2
Primary Topic
Supramolecular Self-Assembly in Materials
Type
article
Field-Weighted Citation Impact
0.35
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article

Conjugated Nanobelts Based on N -Hetero[(6.) m 8] n cyclacene

Yongming Xiong, Lin Xue, Naoki Aratani, Chenyu Hu et al.
2 citations
CCS Chemistry
Supramolecular Self-Assembly in Materials
0.35
article

Conjugated Nanobelts Based on N -Hetero[(6.) m 8] n cyclacene

Yongming Xiong, Lin Xue, Naoki Aratani, Chenyu Hu, H. J. Yang, Qian Miao
article en
2 citations

Abstract

<span>This study introduces a novel design of </span><i>N</i><span>-doped conjugated nanobelts, derived from a specific structural unit found in carbon schwarzites, a type of negatively curved carbon allotrope. The successful synthesis of these nanobelts was achieved using a flexible curved building block in a condensation reaction with </span><i>ortho</i><span>-quinones. The electronic structure and aromaticity of the diazatetracene-based nanobelt were investigated and compared with diazatetracene dimers through a combination of computational and experimental methods, revealing the influence of macrocyclization on these attributes. Notably, the diazatetracene-based nanobelt encapsulates C</span><span>70</span><span> in toluene with a high binding constant of (2.8 ± 0.2) × 10</span><span>5</span><span> M</span><span>−1</span><span>, demonstrating significant selectivity against C</span><span>60</span><span>. X-ray crystallographic analysis indicated that the nanobelt adjusts its rhombus cross section to enhance host–guest interactions when accommodating C</span><span>70</span><span>.</span>

CCS ChemistryVol. 7(6)
Chinese University of Hong Kong (HK), State Key Laboratory of Synthetic Chemistry (CN), Nara Institute of Science and Technology (JP), University of Hong Kong (HK)
Openalex Percentile: Top 42%
Supramolecular Self-Assembly in Materials
0.35
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