論文 On-Surface Synthesis of Azobenzene-Linked Porphyrin Derivatives

Yuji Isshiki ORCID (National Institute for Materials Science) ; Donglin Li ORCID (National Institute for Materials Science) ; Saranyan Vijayaraghavan (CSIR-Central Electrochemical Research Institute) ; Kewei Sun SAMURAI ORCID (National Institute for Materials Science) ; Huynh Thien Ngo (National Institute for Materials Science) ; Luiza Buimaga-Iarinca (National Institute for Research and Development of Isotopic and Molecular Technologies) ; Yoshitaka Matsushita SAMURAI ORCID (National Institute for Materials Science) ; Edward A. Neal (National Institute for Materials Science) ; Cristian Morari (National Institute for Research and Development of Isotopic and Molecular Technologies) ; Jonathan P. Hill SAMURAI ORCID (National Institute for Materials Science) ; Shigeki Kawai SAMURAI ORCID (National Institute for Materials Science)

コレクション

引用
Yuji Isshiki, Donglin Li, Saranyan Vijayaraghavan, Kewei Sun, Huynh Thien Ngo, Luiza Buimaga-Iarinca, Yoshitaka Matsushita, Edward A. Neal, Cristian Morari, Jonathan P. Hill, Shigeki Kawai. On-Surface Synthesis of Azobenzene-Linked Porphyrin Derivatives. The Journal of Physical Chemistry Letters. 2025, 16 (45), 11833-11841. https://doi.org/10.1021/acs.jpclett.5c03174

説明:

(abstract)

On-surface synthesis has become an attractive strategy to obtain functionalized carbon nanostructures from small precursor molecules using a bottom-up approach. Although various on-surface reactions have been developed, it is still unclear how the chirality of self-assembled structures prior to reaction affects the coupling process. Here, we investigate homocoupling of nitro-phenyl groups in Pt-porphyrin derivatives on Au(111) surfaces using low-temperature scanning tunneling microscopy. Two different self-assembled structures composed either of linear oligomer of molecules of opposing chirality or of discrete trimers of molecules having the same chirality (i.e., homochiral) were respectively obtained by using differently substituted phenyl and 3,5-di-tert-butylphenyl groups porphyrin cores. A machine-learning-assisted protocol was used for large-scale statistical analysis revealing the distinct difference in reaction yields of azobenzene formation between two different self-assembled structures. Since the azobenzene (dimer) products are composed of two molecules with opposing chirality (i.e., they are heterochiral), the molecules in the homochiral assembly must first be disassembled, which is one of the reasons for the low reaction yield. This study highlights the significant role of porphyrin chirality in the azo coupling reaction process on surface.

権利情報:

キーワード: On-surface synthesis, scanning tunneling microscopy, chirality, porphyrin derivatives, azobenzene, molecular structure, pyrroles

刊行年月日: 2025-11-13

出版者: American Chemical Society (ACS)

掲載誌:

  • The Journal of Physical Chemistry Letters (ISSN: 19487185) vol. 16 issue. 45 p. 11833-11841

研究助成金:

  • Japan Society for the Promotion of Science 24KF0269
  • Japan Society for the Promotion of Science 25H00422
  • Ministerul Cercetarii, Inovarii si Digitalizarii PN23 24 01 04
  • Japan Society for the Promotion of Science 24K21721

原稿種別: 出版者版 (Version of record)

MDR DOI:

公開URL: https://doi.org/10.1021/acs.jpclett.5c03174

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更新時刻: 2025-11-20 12:30:19 +0900

MDRでの公開時刻: 2025-11-20 12:24:30 +0900

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