Supporting Information
Supporting information features copies of 1H and 13C NMR spectra and UV-vis absorption spectra of compound 1 and Cartesian coordinates of the optimized structure of 1.
| Supporting Information File 1: UV–vis spectra, NMR spectra and Cartesian coordinates. | ||
| Format: PDF | Size: 1.3 MB | Download |
| Supporting Information File 2: Crystallographic information file of compound 1. | ||
| Format: CIF | Size: 303.9 KB | Download |
Cite the Following Article
Six-fold C–H borylation of hexa-peri-hexabenzocoronene
Mai Nagase, Kenta Kato, Akiko Yagi, Yasutomo Segawa and Kenichiro Itami
Beilstein J. Org. Chem. 2020, 16, 391–397.
https://doi.org/10.3762/bjoc.16.37
How to Cite
Nagase, M.; Kato, K.; Yagi, A.; Segawa, Y.; Itami, K. Beilstein J. Org. Chem. 2020, 16, 391–397. doi:10.3762/bjoc.16.37
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Presentation Graphic
| Picture with graphical abstract, title and authors for social media postings and presentations. | ||
| Format: PNG | Size: 129.6 KB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Maddala, S.; Mahanthi, S.; Parthasarathy, V. Navigating Scholl-Type Oxidative Coupling: An Electronic Programming Toward Path Revelation, Selectivity, and Control. Chemistry (Weinheim an der Bergstrasse, Germany) 2025, 31, e01724. doi:10.1002/chem.202501724
- Sanematsu, H.; Bulgarevich, K.; Dhara, B.; Takimiya, K. Synthesis of Parent Peropyrene and Its Derivatization. Organic letters 2025, 27, 5948–5952. doi:10.1021/acs.orglett.5c01172
- Zheng, X.; Gupta, N.; He, H.; Bindra, J. K.; Hossain, S.; Vizuet, J. P.; Nadeali, A.; Zangeneh, D.; Singh, R. P.; Klie, R. F.; Chaplin, B. P.; Brezinsky, K.; Poluektov, O. G.; Niklas, J.; Zapol, P.; Glusac, K. D. A Light-Responsive Metal-Organic Framework with Perchlorinated Nanographene Ligands. Journal of the American Chemical Society 2025, 147, 16420–16428. doi:10.1021/jacs.5c02844
- Kavitha, M.; Krishnan, S. Analyzing Weighted Mostar Invariants in Polycyclic Aromatic Compounds. Elsevier BV 2025. doi:10.2139/ssrn.5128882
- Zhang, X.; Li, D.; Tan, C. C. H.; Hanindita, F.; Hamamoto, Y.; Foster, A. S.; Kawai, S.; Ito, S. Synthesis of azahexabenzocoronenium salts through a formal [3 + 3] cycloaddition strategy. Nature Synthesis 2024, 3, 1283–1291. doi:10.1038/s44160-024-00595-5
- Van Raden, J. M.; Deng, J.; Gotfredsen, H.; Hergenhahn, J.; Clarke, M.; Edmondson, M.; Hart, J.; O'Shea, J. N.; Duarte, F.; Saywell, A.; Anderson, H. L. Template‐Directed Synthesis of Strained meso‐meso‐Linked Porphyrin Nanorings. Angewandte Chemie 2024, 136. doi:10.1002/ange.202400103
- Van Raden, J. M.; Deng, J.-R.; Gotfredsen, H.; Hergenhahn, J.; Clarke, M.; Edmondson, M.; Hart, J.; O'Shea, J. N.; Duarte, F.; Saywell, A.; Anderson, H. L. Template-Directed Synthesis of Strained meso-meso-Linked Porphyrin Nanorings. Angewandte Chemie (International ed. in English) 2024, 63, e202400103. doi:10.1002/anie.202400103
- Gunasekar, T.; Kathavarayan, P.; Alsinai, A.; Murugan, G. On Certain Degree Based and Bond-additive Topological Indices of Dodeca-benzo-circumcorenene. Combinatorial chemistry & high throughput screening 2024, 27, 1629–1641. doi:10.2174/0113862073274943231211110011
- Murugan, G.; Julietraja, K.; Alsinai, A. Computation of Neighborhood M-Polynomial of Cycloparaphenylene and Its Variants. ACS omega 2023, 8, 49165–49174. doi:10.1021/acsomega.3c07294
- Yu, I. F.; Wilson, J. W.; Hartwig, J. F. Transition-Metal-Catalyzed Silylation and Borylation of C-H Bonds for the Synthesis and Functionalization of Complex Molecules. Chemical reviews 2023, 123, 11619–11663. doi:10.1021/acs.chemrev.3c00207
- Usman, M.; Javaid, M. Connection-Based Zagreb Indices of Polycyclic Aromatic Hydrocarbons Structures. Current organic synthesis 2023, 21, 246–256. doi:10.2174/1570179421666230823141758
- Hogan, D. T.; Zhou, W.; Gelfand, B. S.; Sutherland, T. C. Rational assembly of benzenoid rings in benzo[ghi]perylene yields a diversity of edge features with site-selective reactivity. Organic Chemistry Frontiers 2023, 10, 3467–3478. doi:10.1039/d3qo00718a
- Cooper, C. T. Ph.D. Thesis, University of North Texas Libraries, July 1, 2023. doi:10.12794/metadc2179339
- Arockiaraj, M.; Kavitha, S. R. J.; Klavžar, S.; Fiona, J. C.; Balasubramanian, K. Topological, Spectroscopic and Energetic Properties of Cycloparaphenylene Series. Polycyclic Aromatic Compounds 2023, 44, 1072–1094. doi:10.1080/10406638.2023.2186442
- Segawa, Y.; Nagase, M.; Saito, Y.; Kato, K.; Itami, K. C-H Borylation of Arenes: Steric-controlled Para-selectivity and Application to Molecular Nanocarbons. Journal of Synthetic Organic Chemistry, Japan 2022, 80, 994–999. doi:10.5059/yukigoseikyokaishi.80.994
- Kim, Y.-j.; Kang, M.; Kim, Y. H.; Suh, E.-K.; Yang, M.; Cho, S. Y.; Jeon, D.-Y.; Kim, J. G.; Kim, J.; Ahn, S. Contorted hexabenzocoronene derivatives as a universal organic precursor for dimension-customized carbonization. Carbon 2022, 200, 21–27. doi:10.1016/j.carbon.2022.08.049
- Segawa, Y. Nonplanar Aromatic Hydrocarbons: Design and Synthesis of Highly Strained Structures. Bulletin of the Chemical Society of Japan 2022, 95, 1600–1610. doi:10.1246/bcsj.20220270
- Govardhan, S.; Roy, S.; Prabhu, S.; Siddiqui, M. K. Computation of Neighborhood M-Polynomial of Three Classes of Polycyclic Aromatic Hydrocarbons. Polycyclic Aromatic Compounds 2022, 43, 5519–5535. doi:10.1080/10406638.2022.2103576
- Arulperumjothi, M.; Prabhu, S.; Liu, J.-B.; Rajasankar, P. Y.; Gayathri, V. On counting polynomials of certain classes of polycyclic aromatic hydrocarbons. Polycyclic Aromatic Compounds 2022, 43, 4768–4786. doi:10.1080/10406638.2022.2094969
- Radhakrishnan, M.; Prabhu, S.; Arockiaraj, M.; Arulperumjothi, M. Molecular structural characterization of superphenalene and supertriphenylene. International Journal of Quantum Chemistry 2021, 122. doi:10.1002/qua.26818