Evidence map›Paper›PMID 41466131›Full record

ArticleCommunications chemistry2025

Time-evolving photoreconfigurable self-assembly for integrated fluorochromic cellulosic emitter.

Fengfan Zhu, Xiao-Fang Hou, Hongyang Zhang, Juping Wang, Naixu Li, Bo Fu, Jiancheng Zhou, Xu-Man Chen

Abstract read
In one paragraph

Article in Communications chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Fengfan ZhuSchool of Chemistry and Chemical Engineering, Southeast University, Nanjing, China.ORCID http://orcid.org/0000-0001-6519-8140
Xiao-Fang HouSchool of Chemistry and Chemical Engineering, Southeast University, Nanjing, China.
Hongyang ZhangSchool of Chemistry and Chemical Engineering, Southeast University, Nanjing, China.
Juping WangSchool of Chemistry and Chemical Engineering, Southeast University, Nanjing, China.
Naixu LiSchool of Chemistry and Chemical Engineering, Southeast University, Nanjing, China.ORCID http://orcid.org/0000-0002-0524-5475
Bo FuJiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, College of Chemical Engineering, Nanjing Forestry University, Nanjing, China.
Jiancheng ZhouSchool of Chemistry and Chemical Engineering, Southeast University, Nanjing, China. jczhou@seu.edu.cn.ORCID http://orcid.org/0000-0002-5551-782X
Xu-Man ChenSchool of Chemistry and Chemical Engineering, Southeast University, Nanjing, China. chenxm@seu.edu.cn.ORCID http://orcid.org/0000-0002-3077-5806

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Light-driven dissipative self-assembly has garnered substantial attention due to its precise spatiotemporal controllability. However, achieving synergistic integration of spatial manipulation fidelity, architectural programmability, and dynamic reconfigurability within a free-standing platform remains a formidable challenge. Herein, we report a light-driven hierarchical dissipative self-assembly paradigm with temporally programmable fluorochromism, achieved through molecular-engineered coordination of dynamic macrocyclic host-guest interactions within sustainable cellulose matrices. Protonated vinylpyridium-derived merocyanine is designed and synthesized to construct light-controlled differential binding architectures with cucurbiturils. This system demonstrates quantitatively reversible interconversion between spiropyran and merocyanine states through alternating photoactivation (475 nm) and thermal relaxation. Structural modulation of host-guest stoichiometry between 1:2 and 1:1 induces nanoscale morphological switching between spherical and cuboid assemblies, accompanied by time-resolved fluorescence chromism. Leveraging the inherent affinity between cucurbiturils and cellulose nanofibrils, we engineered light-fueled hierarchical architectures into freestanding cellulosic papers, exhibiting self-erasing transient photowriting and multilevel anti-counterfeiting functions. The non-covalent host-guest architecture and reprocessable cellulose matrix synergistically enable material recyclability. This spatiotemporally programmed dissipative self-assembly system pioneers sustainable cellulose platforms for adaptive optoelectronics and smart sensing.

Identifiers

PMID41466131
PMCPMC12864956

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.