Non‐Buckling Stacks of Nanocarbon Molecules

ABSTRACT An octagon‐centered nanocarbon molecule, phenine dehydrogenated tetramethano‐ o ‐tetraphene (phenine dH‐ToT), is reported. The synthesis employed machine‐learning‐augmented concentration‐dependent yield analysis (ML+CYAN) to optimize a tetrameric macrocyclization while simultaneously extracting kinetic information. Crystallographic analysis revealed a unique molecular structure featuring a flattened octagon center surrounded by alternating pentagon and hexagon rims with slight buckling. In the crystal, two molecules were azimuthally offset to form an S 8 ‐symmetric dimer stack with a pentagon‐over‐hexagon arrangement. Detailed variable‐temperature NMR studies revealed that the S 8 ‐dimer was assembled in an entropy‐driven manner and remains frozen without buckling dynamics in solution, in contrast to the rapid buckling dynamics observed for saddle‐shaped phenine [ n ]circulene dimers. Upon dissociation into monomers, phenine dH‐ToT was liberated to undergo buckling dynamics and was observed as a time‐averaged D 4h ‐symmetric species. These results demonstrate the key role of polygonal arrangements in controlling buckling dynamics in nanocarbon bilayer stacks.

Authors

Institutions

Publication Details

Journal
Angewandte Chemie International Edition
Published
2026-10-28
DOI
https://doi.org/10.1002/anie.1589029
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Non‐Buckling Stacks of Nanocarbon Molecules

礼二郎 山本, T. Fukunaga, Shunji Takemura, Hiroyuki Isobe et al.
Angewandte Chemie International Edition
Synthesis and Properties of Aromatic Compounds
article

Non‐Buckling Stacks of Nanocarbon Molecules

礼二郎 山本, T. Fukunaga, Shunji Takemura, Hiroyuki Isobe, Koki Ikemoto, Renki Sakai, Xinyi Xiao, Yuzuka Shoji, Elisa Nobre
article en

Abstract

ABSTRACT An octagon‐centered nanocarbon molecule, phenine dehydrogenated tetramethano‐ o ‐tetraphene (phenine dH‐ToT), is reported. The synthesis employed machine‐learning‐augmented concentration‐dependent yield analysis (ML+CYAN) to optimize a tetrameric macrocyclization while simultaneously extracting kinetic information. Crystallographic analysis revealed a unique molecular structure featuring a flattened octagon center surrounded by alternating pentagon and hexagon rims with slight buckling. In the crystal, two molecules were azimuthally offset to form an S 8 ‐symmetric dimer stack with a pentagon‐over‐hexagon arrangement. Detailed variable‐temperature NMR studies revealed that the S 8 ‐dimer was assembled in an entropy‐driven manner and remains frozen without buckling dynamics in solution, in contrast to the rapid buckling dynamics observed for saddle‐shaped phenine [ n ]circulene dimers. Upon dissociation into monomers, phenine dH‐ToT was liberated to undergo buckling dynamics and was observed as a time‐averaged D 4h ‐symmetric species. These results demonstrate the key role of polygonal arrangements in controlling buckling dynamics in nanocarbon bilayer stacks.

Angewandte Chemie International Edition
The University of Tokyo (JP)
Openalex Percentile: Top 25%
Synthesis and Properties of Aromatic Compounds
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon
Non‐Buckling Stacks of Nanocarbon Molecules — 礼二郎 山本, T. Fukunaga, et al. · Angewandte Chemie International Edition (2026) | TGRS Research Map | TGRS