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Cited by 596

The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.

The Strong Light‐Emission Materials in the Aggregated State: What Happens from a Single Molecule to the Collective Group

Open access
Li, Qianqian, Li, Zhen·2017·Advanced Science

Abstract

The strong light emission of organic luminogens in the aggregated state is essential to their applications as optoelectronic materials with good performance. In this review, with respect to the aggregation‐induced emission and room‐temperature phosphorescence luminogens, the important role of molecular packing modes is highlighted. As demonstrated in the selected examples, the molecular packing status in the aggregate state is affected by many factors, including the molecular configurations, the inherent electronic properties, the special functional groups, and so on. With the consideration of all these parameters, the strong fluorescence and phosphorescence in the aggregated state could be achieved in the rationally designed organic luminogens, providing some guidance for the further development.

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Crossref · 10.1002/advs.201600484

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Metadata

Authors
Li, Q., & Li, Z.
Venue
Advanced Science
Publisher
Wiley
Published
2017-02-21
Volume
4
Issue
7
Pages
1600484-1600484
ISSN
2198-3844 (ISSN-L)
OpenAlex
W2590866645
Cited by
596
References
7
FWCI
30.26
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: The Strong Light‐Emission Materials in the Aggregated State: What Happens from a Single Molecule to the Collective Group. https://app.cochat.ai/papers/10.1002/advs.201600484
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Li, Q., & Li, Z. (2017). The Strong Light‐Emission Materials in the Aggregated State: What Happens from a Single Molecule to the Collective Group. Advanced Science. https://doi.org/10.1002/advs.201600484

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.