Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Nature Communications
  • View all journals
  • Search
  • My Account Login
  • Content Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • RSS feed
  1. nature
  2. nature communications
  3. articles
  4. article
Topology-controlled dynamic conjugated oligomers from tetra-arylsubstituted alkene building blocks
Download PDF
Download PDF
  • Article
  • Open access
  • Published: 28 February 2026

Topology-controlled dynamic conjugated oligomers from tetra-arylsubstituted alkene building blocks

  • Qilong Bian1,2,
  • Ying Zhao1,2,
  • Chunhua Zhang3,
  • Yang Zhang1,2,
  • Yang Zhang4,
  • Zebing Zeng  ORCID: orcid.org/0000-0002-6246-39111,2,
  • Ben Zhong Tang  ORCID: orcid.org/0000-0002-0293-964X5 &
  • …
  • Sheng Xie  ORCID: orcid.org/0009-0007-9728-64961,2 

Nature Communications , Article number:  (2026) Cite this article

  • 2003 Accesses

  • Metrics details

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Conjugated polymers
  • Polymer synthesis
  • Self-assembly

Abstract

Topology plays an important role in polymeric materials. Herein, we present an iterative, modular approach for creating tetra-arylsubstituted alkene (TAA)-based dynamic conjugated oligomers with diverse topologies, using boronate-protected Suzuki-Miyaura coupling chemistry. The TAA building blocks involving spontaneous alkene isomerization are found to induce conformational dynamics in the conjugated backbones, exhibiting steric-controlled transitions. These transitions occur from a twisted backbone rich in cis-alkenes in the linear PL9 oligomer, to a stretched backbone with a trans-alkene center and multiple cis-alkene end in the three-armed planar PY12 oligomer and the four-armed 3D PX16 oligomer. Consequently, these topological oligomers exhibit distinct photoluminescence and photochemical properties depending on their physical state. Experimental characterization and molecular dynamics simulations (MD) reveal a topology-dependent adaptive self-assembly of helices: linear PL9 forms long flexible helical fibers with a pitch of 28 nm; planar Y-type PY12 oligomers often occur in neural-like networks, connected by nanofibers and cell-like central aggregates; and stereo X-type PX16 adopts short helical rod-like morphology with a mesoscopic pitch of 86 nm in crystalline phases. This work may inspire concepts and the practical construction of helical and neural-like fiber materials by altering unit topology in dynamic conjugated oligomers.

Similar content being viewed by others

Electro-mechanically switchable hydrocarbons based on [8]annulenes

Article Open access 14 February 2022

Controlling the helicity of π-conjugated oligomers by tuning the aromatic backbone twist

Article Open access 21 January 2022

Photocatalytic Stereoselective Editing of Alkynes to 3D Molecules via Hydrogen Atom Transfer-Mediated Dynamic Epimerization

Article Open access 09 February 2026

Data availability

The data supplementary the findings of this study are available in the article. All data are available from the corresponding author upon request. Source Data are provided with this manuscript. The data in this manuscript do not include clinical data or third-party data; all data originate from the authors’ experimental work. The experimental characterization and computational data generated in this paper are provided in the supplementary information. Source data are provided with this paper.

References

  1. Hemminger, J. et al. From quanta to the continuum: opportunities for mesoscale science. U.S. Department of Energy, 3-11 (Argonne National Laboratory, United States, (2012).

  2. Hughes, J., Tran, C. & Rappporteurs, J. A. Mesoscale chemistry: a workshop summary. National Academies Press, 2–8 (Washington, DC, 2015).

  3. Tu, Y., Zhao, Z., Lam, J. W. Y. & Tang, B. Z. Aggregate science: much to explore in the meso world. Matter 4, 338–349 (2021).

    Google Scholar 

  4. Zhang, B., Watuthanthrige, N. D. A., Wanasinghe, S. V., Averick, S. & Konkolewicz, D. Complementary dynamic chemistries for multifunctional polymeric materials. Adv. Funct. Mater. 32, 2108431 (2022).

    Google Scholar 

  5. Ni, Z. et al. Mesopolymer synthesis by ligand-modulated direct arylation polycondensation towards n-type and ambipolar conjugated systems. Nat. Chem. 11, 271–277 (2019).

    Google Scholar 

  6. Genabeek, B. V. et al. Properties and applications of precision oligomer materials; where organic and polymer chemistry join forces. J. Polym. Sci. 59, 373–403 (2021).

    Google Scholar 

  7. Shi, Q., Deng, Z., Hou, M., Hu, X. & Liu, S. Engineering precise sequence-defined polymers for advanced functions. Prog. Polym. Sci. 141, 101677 (2023).

    Google Scholar 

  8. Murphy, E. A., Zhang, C., Bates, C. M. & Hawker, C. J. Chromatographic separation: a versatile strategy to prepare discrete and well-defined polymer libraries. Acc. Chem. Res. 57, 1202–1213 (2024).

    Google Scholar 

  9. Pasgrimaud, C. et al. Synthesis of electron-deficient BisAzaCoroneneDiimide-conjugated polymers by light-locking dynamic covalent bonds. J. Am. Chem. Soc. 147, 12218–12227 (2025).

    Google Scholar 

  10. Anderson, P. W. More is different. Science 177, 393–396 (1972).

    Google Scholar 

  11. Barua, H., Svärd, M., Rasmuson, ÅC., Hudson, S. P. & Cookman, J. Mesoscale clusters in the crystallisation of organic molecules. Angew. Chem. Int. Ed. 63, e202312100 (2024).

    Google Scholar 

  12. Zhang, Y., Xie, S., Zeng, Z. & Tang, B. Z. Functional scaffolds from AIE building blocks. Matter 3, 1862–1892 (2020).

    Google Scholar 

  13. Xu, G. et al. -Cyano triaryl[3]radialene: unsymmetrical stereo-configuration, clustering-enhanced excimer emission, and radical-involved multimodal information switching. Angew. Chem. Int. Ed. 62, e202305011 (2023).

    Google Scholar 

  14. Wang, X. et al. Photoelectromagnetic responsive adaptive porous frameworks through dynamic covalent chemistry of tetraarylethylene-backboned aryldicyanomethyl radicals. Angew. Chem. Int. Ed. 62, e202301719 (2023).

    Google Scholar 

  15. Liu, H. et al. A photoelectromagnetic 3D metal-organic framework from flexible tetraarylethylene-backboned ligand and dynamic copper-based coordination chemistry. Small 20, 2306956 (2024).

    Google Scholar 

  16. Meng, S. et al. Anisotropic flexibility and rigidification in a TPE-based Zr-MOFs with scutopology. Nat. Commun. 14, 5347 (2023).

    Google Scholar 

  17. Wang, S., Zhang, Q., Wang, Z., Guan, S. & Zhang, X. Tetraphenylethylene-based hydrogen-bonded organic frameworks (HOFs) with brilliant fluorescence. Angew. Chem. Int. Ed. 62, e202315382 (2023).

    Google Scholar 

  18. Li, C., Zhao, W., He, J. & Zhang, Y. Topology controlled all- (meth) acrylic thermoplastic elastomers by multi-functional Lewis pairs-mediated polymerization. Angew. Chem. Int. Ed. 63, e202401265 (2024).

    Google Scholar 

  19. Irie, M., Fukaminato, T., Matsuda, K. & Kobatake, S. Photochromism of diarylethene molecules and crystals: memories, switches, and actuators. Chem. Rev. 114, 12174–12277 (2014).

    Google Scholar 

  20. Zhou, Z. et al. Spiro-functionalized diphenylethenes: suppression of a reversible photocyclization contributes to the aggregation-induced emission effect. J. Am. Chem. Soc. 141, 9803–9807 (2019).

    Google Scholar 

  21. Xie, Y. & Li, Z. Recent advances in the Z/E isomers of tetraphenylethene derivatives: stereoselective synthesis, AIE mechanism, photophysical properties, and application as chemical probes. Chem. Asian J. 14, 2524–2541 (2019).

    Google Scholar 

  22. Huang, Y. et al. Tuning proapoptotic activity of a phosphoric-acid-tethered tetraphenylethene by visible-light-triggered isomerization and switchable protein interactions for cancer therapy. Angew. Chem. Int. Ed. 61, e202208378 (2022).

    Google Scholar 

  23. Huang, Y., Zhang, G., Zhao, R. & Zhang, D. Tetraphenylethene-based cis/trans isomers for targeted fluorescence sensing and biomedical applications. Chem. Eur. J. 29, e202300539 (2023).

    Google Scholar 

  24. Liu, X., Li, Y., Li, X. & Hahn, F. E. Photoinduced E to Z isomerization of tetraphenylethylene derivatives within organometallic supramolecular assemblies. Sci. China Chem. 64, 1709–1715 (2021).

    Google Scholar 

  25. Yu, X. Trans/cis-stereoisomers of triterpenoid-substituted tetraphenylethene: aggregation-induced emission, aggregate morphology, and mechano-chromism. Nanoscale 13, 15257–15266 (2021).

    Google Scholar 

  26. Nie, X. et al. Kinetic and thermodynamic control of tetraphenylethene aggregation-induced emission behaviors. Aggregate 3, e165 (2022).

    Google Scholar 

  27. Bian, Q. et al. Iterative synthesis of dynamic conjugated oligomers displaying length-dependent configuration metastability, state-dependent properties, and helix emergence. Angew. Chem. Int. Ed. 64, e202505703 (2025).

    Google Scholar 

  28. Xia, Q. et al. Direct visualization of chiral ampli fication of chiral aggregation induced emission molecules in nematic liquid crystals. ACS Nano 15, 4956–4966 (2021).

    Google Scholar 

  29. Li, Z. et al. Visual β-sheet-to-β-turn transition in luminescent polymeric vesicles for color-reporting drug delivery. Angew. Chem. Int. Ed. 64, e202503875 (2025).

    Google Scholar 

  30. Wu, Z. et al. Dynamic cross-linked topological network reconciles the longstanding contradictory properties of polymers. Sci. Adv. 11, e0825 (2025).

    Google Scholar 

  31. Webber, M. J. & Tibbitt, M. W. Dynamic and reconfigurable materials from reversible network interactions. Nat. Rev. Mater. 7, 541–556 (2022).

    Google Scholar 

  32. Fang, Z. et al. 3D printing of dynamic covalent polymer network with on-demand geometric and mechanical reprogrammability. Nat. Commun. 14, 1313 (2023).

    Google Scholar 

  33. Reith, M. A. et al. Sequence-dezined mikto-arm star-shaped macromolecules. J. Am. Chem. Soc. 144, 7236–7244 (2022).

    Google Scholar 

  34. Reilly, L. T., Kottage, D., Cavallo, L., Falivene, L. & Chen, E. Y. Entropy-regulated selective synthesis of cyclic polymers and polycatenanes by Lewis pair polymerization. J. Am. Chem. Soc. 147, 31689–31703 (2025).

    Google Scholar 

  35. Weil, T. & Chen, C. Cyclic polymers: synthesis, characteristics, and emerging applications. Nanoscale Horiz. 7, 1121–1135 (2022).

    Google Scholar 

  36. Xu, C. et al. Regio- and sequence-controlled conjugated topological oligomers and polymers via boronate-tag assisted solution-phase strategy. Nat. Commun. 12, 5853 (2021).

    Google Scholar 

  37. Yin, J., Choi, S., Pyle, D., Guest, J. R. & Dong, G. Backbone engineering of monodisperse conjugated polymers via integrated iterative binomial synthesis. J. Am. Chem. Soc. 145, 19120–19128 (2023).

    Google Scholar 

  38. Mills, H. A. et al. Sequence-defined conjugated oligomers in donor-acceptor dyads. J. Am. Chem. Soc. 145, 23519–23526 (2023).

    Google Scholar 

  39. Li, Z. & Tang, Y. Stair-like narrow N-doped nanographene with unusual diradical character at the topological interface. Chem 9, 1–14 (2023).

    Google Scholar 

  40. Kim, M. P. et al. Iterative SuFEx approach for sequence-regulated oligosulfates and its extension to periodic copolymers. Nat. Commun. 15, 3381 (2024).

    Google Scholar 

  41. Lai, Y. et al. Modulating ligand-exchange dynamics on metal-organic polyhedra for reversible sorting and hybridization of miktoarm star polymers. Angew. Chem. Int. Ed. 62, e202311954 (2023).

    Google Scholar 

  42. Gkolfi, E. & Harmandaris, V. Soft character of star-like polymer melts: from linear-like chains to impenetrable nanoparticles. Nano Lett. 23, 1608–1614 (2023).

    Google Scholar 

  43. Hu, R., Leung, N. L. C. & Tang, B. Z. AIE macromolecules: syntheses, structures and functionalities. Chem. Soc. Rev. 43, 4494–4562 (2014).

    Google Scholar 

  44. Aida, T., Meijer, E. W. & Stupp, S. I. Functional supramolecular polymers. Science 335, 813–817 (2012).

    Google Scholar 

  45. Zhang, G., Cheng, X., Wang, Y. & Zhang, W. Supramolecular chiral polymeric aggregates: construction and applications. Aggregate 4, e262 (2023).

    Google Scholar 

  46. Wang, W. et al. Rapid automated iterative small-molecule synthesis. Nat. Synth. 3, 1031–1038 (2024).

    Google Scholar 

  47. Xu, C., Dong, J., He, C., Yun, J. & Pan, X. Precise control of conjugated polymer synthesis from step-growth polymerization to iterative synthesis. Giant 14, 100154 (2023).

    Google Scholar 

  48. Blair, D. J. et al. Automated iterative Csp3-C bond formation. Nature 604, 92–97 (2022).

    Google Scholar 

  49. Lehmann, J. W., Blair, D. J. & Burke, M. D. Towards the generalized iterative. Nat. Rev. Chem. 2, 0115 (2018).

    Google Scholar 

Download references

Acknowledgements

This work was supported by the National Natural Science Foundation of China (52525306 and 22375059), Shenzhen Science and Technology Innovation Program (JCYJ20220530160403008), and Natural Science Foundation of Hunan Province (2023JJ50002 and 2024RC1027). Thanks to the Analytical Instrumentation Center of Hunan University, and the AIE institute (www.aietech.org.cn) for providing technical assistance.

Author information

Authors and Affiliations

  1. State Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, Hunan University, Changsha, China

    Qilong Bian, Ying Zhao, Yang Zhang, Zebing Zeng & Sheng Xie

  2. Shenzhen Research Institute of Hunan University, Nanshan District, Shenzhen, China

    Qilong Bian, Ying Zhao, Yang Zhang, Zebing Zeng & Sheng Xie

  3. School of Physics and Telecommunications Engineering, Zhoukou Normal University, Zhoukou, China

    Chunhua Zhang

  4. Analytical Instrumentation Center of Hunan University, Hunan University, Changsha, China

    Yang Zhang

  5. Guangdong Basic Research Center of Excellence for Aggregate Science, School of Science and Engineering, The Chinese University of Hong Kong, Shenzhen, China

    Ben Zhong Tang

Authors
  1. Qilong Bian
    View author publications

    Search author on:PubMed Google Scholar

  2. Ying Zhao
    View author publications

    Search author on:PubMed Google Scholar

  3. Chunhua Zhang
    View author publications

    Search author on:PubMed Google Scholar

  4. Yang Zhang
    View author publications

    Search author on:PubMed Google Scholar

  5. Yang Zhang
    View author publications

    Search author on:PubMed Google Scholar

  6. Zebing Zeng
    View author publications

    Search author on:PubMed Google Scholar

  7. Ben Zhong Tang
    View author publications

    Search author on:PubMed Google Scholar

  8. Sheng Xie
    View author publications

    Search author on:PubMed Google Scholar

Contributions

S.X., Z.Z., and B.Z.T. designed the research. Q.B., Ying Zhao, C.Z., Y.Z. ‘affiliation 1’, and Y.Z. ‘affiliation 3’ performed the research. Q.B. and S.X. conducted the analyses. S.X., Z.Z., and B.Z.T. supervised the research. Q.B. and S.X. wrote the paper. All authors substantially revised and edited the manuscript.

Corresponding authors

Correspondence to Zebing Zeng, Ben Zhong Tang or Sheng Xie.

Ethics declarations

Competing interests

The authors declare no competing interests.

Peer review

Peer review information

Nature Communications thanks Anna Mielańczyk and the other anonymous reviewers for their contribution to the peer review of this work. A peer review file is available.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Supplementary Information (download PDF )

Description of Additional Supplementary Files (download PDF )

Supplementary Data 1 (download TXT )

Supplementary Data 2 (download TXT )

Supplementary Data 3 (download TXT )

Transparent Peer Review file (download PDF )

Source data

Source Data (download XLSX )

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Bian, Q., Zhao, Y., Zhang, C. et al. Topology-controlled dynamic conjugated oligomers from tetra-arylsubstituted alkene building blocks. Nat Commun (2026). https://doi.org/10.1038/s41467-026-70106-x

Download citation

  • Received: 09 October 2025

  • Accepted: 18 February 2026

  • Published: 28 February 2026

  • DOI: https://doi.org/10.1038/s41467-026-70106-x

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

Download PDF

Advertisement

Explore content

  • Research articles
  • Reviews & Analysis
  • News & Comment
  • Videos
  • Collections
  • Subjects
  • Follow us on Facebook
  • Follow us on X
  • Sign up for alerts
  • RSS feed

About the journal

  • Aims & Scope
  • Editors
  • Journal Information
  • Open Access Fees and Funding
  • Calls for Papers
  • Editorial Values Statement
  • Journal Metrics
  • Editors' Highlights
  • Contact
  • Editorial policies
  • Top Articles

Publish with us

  • For authors
  • For Reviewers
  • Language editing services
  • Open access funding
  • Submit manuscript

Search

Advanced search

Quick links

  • Explore articles by subject
  • Find a job
  • Guide to authors
  • Editorial policies

Nature Communications (Nat Commun)

ISSN 2041-1723 (online)

nature.com footer links

About Nature Portfolio

  • About us
  • Press releases
  • Press office
  • Contact us

Discover content

  • Journals A-Z
  • Articles by subject
  • protocols.io
  • Nature Index

Publishing policies

  • Nature portfolio policies
  • Open access

Author & Researcher services

  • Reprints & permissions
  • Research data
  • Language editing
  • Scientific editing
  • Nature Masterclasses
  • Research Solutions

Libraries & institutions

  • Librarian service & tools
  • Librarian portal
  • Open research
  • Recommend to library

Advertising & partnerships

  • Advertising
  • Partnerships & Services
  • Media kits
  • Branded content

Professional development

  • Nature Awards
  • Nature Careers
  • Nature Conferences

Regional websites

  • Nature Africa
  • Nature China
  • Nature India
  • Nature Japan
  • Nature Middle East
  • Privacy Policy
  • Use of cookies
  • Legal notice
  • Accessibility statement
  • Terms & Conditions
  • Your US state privacy rights
Springer Nature

© 2026 Springer Nature Limited

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing