Synthesis, electronic properties, and self-assembly of an alkylated dibenzo(biscorannulene)
The synthesis and properties of novel aromatic compounds containing fully-conjugated multi-corannulenes are a subject of intense interest. We herein report the synthesis, electronic properties, and self-assembly of alkylated dibenzo(biscorannulene) 1. The properties of 1 are compared with those of t...
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| Published in | ORGANIC CHEMISTRY FRONTIERS Vol. 9; no. 9; pp. 2509 - 2515 |
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| Main Authors | , , , |
| Format | Journal Article |
| Language | English Japanese |
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03.05.2022
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| Abstract | The synthesis and properties of novel aromatic compounds containing fully-conjugated multi-corannulenes are a subject of intense interest. We herein report the synthesis, electronic properties, and self-assembly of alkylated dibenzo(biscorannulene) 1. The properties of 1 are compared with those of the reference compound dibenzocorannulene 2. While the influence of the number of corannulene units on the electronic properties and aromaticity is limited based on UV-vis and emission spectra, electrochemistry, and the results of DFT simulations, the self-assembly behavior is different between molecules of 1 and 2. In H-1 NMR spectra in CDCl3, both compounds show concentration-dependent changes in the chemical shifts of the aromatic hydrogen signals. This indicates self-association, in which the association constant of 1 is greater than that of 2 assuming a monomer-dimer equilibrium. In the crystalline phase, molecules of 1 adopt a parallel-stacked dimer structure through a concave-convex interaction mode, while molecules of 2 form a different structure through a concave-concave interaction mode. DFT simulations of the dimers with different configurations support the increased van der Waals interactions between two fused corannulene units in the stacking geometry. The present results expand the design strategies for gaining control over the organization and functionality of pi-conjugated molecules that contain multiple corannulene units. |
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| AbstractList | The synthesis and properties of novel aromatic compounds containing fully-conjugated multi-corannulenes are a subject of intense interest. We herein report the synthesis, electronic properties, and self-assembly of alkylated dibenzo(biscorannulene) 1. The properties of 1 are compared with those of the reference compound dibenzocorannulene 2. While the influence of the number of corannulene units on the electronic properties and aromaticity is limited based on UV-vis and emission spectra, electrochemistry, and the results of DFT simulations, the self-assembly behavior is different between molecules of 1 and 2. In 1H NMR spectra in CDCl3, both compounds show concentration-dependent changes in the chemical shifts of the aromatic hydrogen signals. This indicates self-association, in which the association constant of 1 is greater than that of 2 assuming a monomer–dimer equilibrium. In the crystalline phase, molecules of 1 adopt a parallel-stacked dimer structure through a concave–convex interaction mode, while molecules of 2 form a different structure through a concave–concave interaction mode. DFT simulations of the dimers with different configurations support the increased van der Waals interactions between two fused corannulene units in the stacking geometry. The present results expand the design strategies for gaining control over the organization and functionality of π-conjugated molecules that contain multiple corannulene units. The synthesis and properties of novel aromatic compounds containing fully-conjugated multi-corannulenes are a subject of intense interest. We herein report the synthesis, electronic properties, and self-assembly of alkylated dibenzo(biscorannulene) 1. The properties of 1 are compared with those of the reference compound dibenzocorannulene 2. While the influence of the number of corannulene units on the electronic properties and aromaticity is limited based on UV-vis and emission spectra, electrochemistry, and the results of DFT simulations, the self-assembly behavior is different between molecules of 1 and 2. In H-1 NMR spectra in CDCl3, both compounds show concentration-dependent changes in the chemical shifts of the aromatic hydrogen signals. This indicates self-association, in which the association constant of 1 is greater than that of 2 assuming a monomer-dimer equilibrium. In the crystalline phase, molecules of 1 adopt a parallel-stacked dimer structure through a concave-convex interaction mode, while molecules of 2 form a different structure through a concave-concave interaction mode. DFT simulations of the dimers with different configurations support the increased van der Waals interactions between two fused corannulene units in the stacking geometry. The present results expand the design strategies for gaining control over the organization and functionality of pi-conjugated molecules that contain multiple corannulene units. |
| Author | Tahara, Kazukuni Hashimoto, Shingo Kunioka, Natsumi Furukawa, Masazumi |
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| Keywords | CORANNULENE PI-STACKING PLANAR RECEPTORS DERIVATIVES POLYARENE MOLECULES |
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| Snippet | The synthesis and properties of novel aromatic compounds containing fully-conjugated multi-corannulenes are a subject of intense interest. We herein report the... |
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| SubjectTerms | Alkylation Aromatic compounds Aromaticity Chemistry Chemistry, Organic Dimers Electrochemistry Emission spectra Molecular structure NMR Nuclear magnetic resonance Organic chemistry Physical Sciences Science & Technology Self-assembly Self-association Synthesis |
| Title | Synthesis, electronic properties, and self-assembly of an alkylated dibenzo(biscorannulene) |
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