journal article·2026-05-26

Asymmetric Double-Spiro Mechanophore in Single-Network and Double-Network Elastomers

Huan Hu, Yongjie Li, Shichao Lian, Qinyao Zhuang, Zheng Gao, Bingjian Zhang, Zhimin Ma, Zhijian Wang, Zhiyong Ma

Chemistry of Materials· Volume 38· Issue 10
Publisher page

Abstract

Asymmetric spiro systems hold promise for eliciting richer stimulus-specific responses, warranting further investigation. In this study, we reported an asymmetric double-spiro mechanophore (named as Fluo-Rh) with the fusion combination of rhodamine and fluorescein. Theoretically, Fluo-Rh has four states of closed–closed (Fluo c -Rh c ), open–closed (Fluo o -Rh c ), closed–open (Fluo c -Rh o ), and open–open (Fluo o -Rh o ) due to its asymmetry. The mechanophore Fluo-Rh was covalently linked into single-network and double-network elastomers with the help of two hydroxyls, and their mechanochromic and photochromic properties were studied. Interestingly, Fluo-Rh underwent ring opening of the fluorescein spiro ring under force but suffered sequential ring opening of both spiro rings (fluorescein spiro ring first) under UV irradiation in the single-network PU. The Fluo o -Rh c state featured the fluorescence band at 562 nm and the absorption bands at 500 and 530 nm. The photoinduced sequential ring opening of Fluo-Rh was reflected by the fluorescence band shift from 555 to 581 nm and the appearance of the absorption band at 432 nm. Only the fluorescein part of the closed ring during heating. However, in the polyurethane-polymethacrylate interpenetrating network (IPN) polymer, only the fluorescein spiro ring can be opened under compression; under UV irradiation, only the rhodamine spiro ring can be opened, showing that the second network inhibits photoinduced ring opening of the fluorescein spiro ring owing to low free volume in IPN. The CoGEF simulation further supported force-induced single ring opening of the fluorescein ring. Compared with the symmetric double-spiro mechanophore, the asymmetric double-spiro mechanophore Fluo-Rh manifested a totally different ring-opening mechanism upon force or UV irradiation. We believe that this work gives deep insight into the double-spiro mechanophore and expands the scope of polymer mechanochemistry.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Force Microscopy Techniques and Applications · Mechanical and Optical Resonators · Advanced Materials and Mechanics

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory of Organic−Inorganic Composites, College of Chemical Engineering

Beijing University of Chemical Technology

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, Center for Soft Matter Science and Engineering, College of Chemistry and Molecular Engineering

Peking University

College of Engineering

Key Laboratory of Aerospace Advanced Materials and Performance, Ministry of Education, School of Materials Science and Engineering

Beihang University

State Key Laboratory of Molecular Engineering of Polymers

Fudan University

Funding

Beijing University of Chemical Technology · Natural Science Foundation of Beijing Municipality · Fundamental Research Funds for the Central Universities · National Natural Science Foundation of China

References (46)

Show source-provided references
1. 10.1021/acs.accounts.5b0018410.1021/acs.accounts.5b00184 ↗
2. 10.1016/j.cej.2025.16151110.1016/j.cej.2025.161511 ↗
3. 10.1002/anie.20251386610.1002/anie.202513866 ↗
4. 10.1021/jacs.4c1565510.1021/jacs.4c15655 ↗
5. 10.1021/jacs.4c1479610.1021/jacs.4c14796 ↗
6. 10.1021/acs.chemrev.5c0078910.1021/acs.chemrev.5c00789 ↗
7. 10.1002/adma.20240376610.1002/adma.202403766 ↗
8. 10.34133/research.039210.34133/research.0392 ↗
9. 10.1039/D0QM00435A10.1039/D0QM00435A ↗
10. 10.1021/jacs.5c1555310.1021/jacs.5c15553 ↗
11. 10.1002/advs.20220532510.1002/advs.202205325 ↗
12. 10.1021/acsami.2c1912110.1021/acsami.2c19121 ↗
13. 10.1126/science.124849410.1126/science.1248494 ↗
14. 10.1021/acs.macromol.4c0229310.1021/acs.macromol.4c02293 ↗
15. 10.1002/adma.20170548310.1002/adma.201705483 ↗
16. 10.1002/adfm.20230536410.1002/adfm.202305364 ↗
17. 10.1002/adma.20180392410.1002/adma.201803924 ↗
18. 10.1002/adfm.20200010510.1002/adfm.202000105 ↗
19. 10.1002/anie.20251328310.1002/anie.202513283 ↗
20. 10.1021/jacs.2c0305610.1021/jacs.2c03056 ↗
21. 10.1002/anie.20250785210.1002/anie.202507852 ↗
22. 10.1016/j.compositesb.2021.10943410.1016/j.compositesb.2021.109434 ↗
23. 10.1002/adma.20251928110.1002/adma.202519281 ↗
24. 10.1016/j.cej.2025.17240410.1016/j.cej.2025.172404 ↗
25. 10.1002/adma.20230216310.1002/adma.202302163 ↗
26. 10.1038/nature0797010.1038/nature07970 ↗
27. 10.1016/j.chempr.2021.02.01410.1016/j.chempr.2021.02.014 ↗
28. 10.1002/anie.20151017110.1002/anie.201510171 ↗
29. 10.1021/jacs.6b0761010.1021/jacs.6b07610 ↗
30. 10.1021/jacs.9b0528010.1021/jacs.9b05280 ↗
31. 10.1021/acsami.7b0017610.1021/acsami.7b00176 ↗
32. 10.1002/adma.20150342410.1002/adma.201503424 ↗
33. 10.1021/acsmacrolett.3c0074910.1021/acsmacrolett.3c00749 ↗
34. 10.1039/c2cp43503a10.1039/c2cp43503a ↗
35. 10.31635/ccschem.023.20230329710.31635/ccschem.023.202303297 ↗
36. 10.1021/acs.macromol.5c0066210.1021/acs.macromol.5c00662 ↗
37. 10.1039/D2PY00728B10.1039/D2PY00728B ↗
38. 10.1021/jacs.2c0701510.1021/jacs.2c07015 ↗
39. 10.1002/anie.20241162910.1002/anie.202411629 ↗
40. 10.1002/anie.20221878510.1002/anie.202218785 ↗
41. 10.1021/acs.macromol.5c0060310.1021/acs.macromol.5c00603 ↗
42. 10.1039/D5SC05757D10.1039/D5SC05757D ↗
43. 10.1039/D3SC03729K10.1039/D3SC03729K ↗
44. 10.1039/D3CC01900D10.1039/D3CC01900D ↗
45. 10.1021/acs.inorgchem.5b0214710.1021/acs.inorgchem.5b02147 ↗
46. 10.1021/jacs.0c0686810.1021/jacs.0c06868 ↗