M. Sugino

若手の会に参加された皆様、3日間お疲れ様でした！

始まりました！

Our new paper is out in Nat. Commun.! 🎉 “Skeletal transformation to chiral nanocarbon molecules” Skeletal transformation solves two challenges in chiral-nanocarbon synthesis. A remarkable achievement made possible by Jun’s enormous effort. 👏 doi.org/10.1038/s41467…

Delighted to share that our new paper has been published in Chem. Eur. J.! Part of this work was conducted during my research stay in the Stefan Hecht lab at Humboldt-Universität zu Berlin🇩🇪 I am deeply grateful for the generous support and guidance. …mistry-europe.onlinelibrary.wiley.com/doi/10.1002/ch…

【受賞】化学専攻の西村里桜さん（博士後期課程３年）が、日本化学会 第106回春季年会（2026）において、学生講演賞を受賞しました！詳細はこちら >> sci.osaka-u.ac.jp/ja/info/16759/

Our recent manuscript, “[3]Cyclo-2,9-peropyrenylene: Longitudinally Curved Peropyrene Nanohoops,” has just been uploaded to ChemRxiv! This project is entirely carried out by my graduate student, Masaya. chemrxiv.org/doi/full/10.26…

Happy to share our the latest paper! B-spiroBODIPYs as a fluorophore responsive to hydrogen bond donors - now published in Organic Chemistry Frontiers pubs.rsc.org/en/content/art…

We just released a press announcement for our recent work published in Angewandte Chemie @angew_chem!! Original paper: onlinelibrary.wiley.com/doi/10.1002/an… Press release (EN): tus.ac.jp/en/mediarelati… Press release (JP) (プレスリリース日本語): tus.ac.jp/today/archive/…

Excited to share our latest paper! We improved the synthesis of anti aromatic norcorroles simply by adding Mn powder! Synthesis of Antiaromatic Ni(II) Norcorroles by Mn Powder | Organic Letters pubs.acs.org/doi/10.1021/ac…

Our paper has been published in Chem. Lett.! We demonstrate that our figure-eight molecule, CBBC, exhibits unique reactivity, enabling the selective transformation. "Nucleophilic Addition to Cyclobisbiphenylenecarbonyl" doi.org/10.1093/chemle…

It is my greatest honor to receive the Chemical Society of Japan Award. I sincerely thank our group members and collaborators. 2025 Award Winners — The Chemical Society of Japan chemistry.or.jp/en/news/2025/2…

第78回日本化学会賞をいただけることになりました。これまで研究を頑張ってくれた学生さん、研究員、スタッフ、共同研究者の皆さんのおかげです。よい仲間に恵まれたことに感謝しています。支えてくれた家族にも感謝！ chemistry.or.jp/news/informati…

Antiaromatic Nanographenes via a BODIPY-Fusion Strategy (@J_A_C_S): pubs.acs.org/doi/10.1021/ja… (@borylation).

新作です。ナノグラフェンにBODIPYを２つ縮環させると反芳香族になるよという論文です。@J_A_C_S pubs.acs.org/doi/10.1021/ja…

Double BODIPY fusion converts the aromaticity of nanographenes into antiaromaticity.@J_A_C_S pubs.acs.org/doi/10.1021/ja…

Our latest manuscript has been uploaded to ChemRxiv! We report the synthesis of a precisely hexabromo-functionalized [9]CPP derivative that serves as a versatile platform for late-stage π-extension to chiral nanohoops with high chiroptical performance. chemrxiv.org/engage/chemrxi…

[Award Accounts] functional π-conjugated molecules, inner modification, molecular design Account by Dr. Norihito Fukui @FukuiNorihito @NagoyaUniv (Nagoya University) #OnTheCover #OpenAccess academic.oup.com/bcsj/article/9…

[3]CycloBODIPY: A Highly Strained Cyclic BODIPY Trimer with Effective Macrocyclic Conjugation (@HTakanoChem, @Borylation): onlinelibrary.wiley.com/doi/10.1002/an… (@angew_chem).

Special issue on π-Conjugated Molecules and Materials in OrgLett is out! pubs.acs.org/page/orlef7/vs…