Stereodefined tetraarylethylenes: Synthesis and applications
Luminescent materials with efficient aggregate‐state emissions are of growing interest due to their widespread applications in chemo‐/biosensing and optoelectronic devices. Aggregation‐induced emission (AIE) opens a new avenue for the applications of aggregate‐state luminescent materials. Among the...
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Published in: | Aggregate (Hoboken) 2021-08, Vol.2 (4), p.n/a |
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Main Authors: | , |
Format: | Article |
Language: | eng |
Subjects: | |
Online Access: | Get full text |
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Summary: | Luminescent materials with efficient aggregate‐state emissions are of growing interest due to their widespread applications in chemo‐/biosensing and optoelectronic devices. Aggregation‐induced emission (AIE) opens a new avenue for the applications of aggregate‐state luminescent materials. Among the AIE luminogens (AIEgens), tetraarylethylenes (TAEs) are typical AIEgens with a simple molecule scaffold and could be utilized as a framework for further elaboration, enabling structure‐property‐function relationship studies and multi‐functional applications. Since the existing approaches for the preparation of tetraarylethenes (TAEs) typically produce stereoisomeric mixtures, stereoselective synthesis of tetraarylethenes with desired geometry is a great challenge. In this review, we systematically compile the synthetic methodologies for the construction of TAEs in excellent regio‐ and stereoselectivities. The virtues and limitations of each methodology are discussed in detail as well. Meanwhile, the applications and the differences of properties between TAEs stereoisomers are introduced.
Among various luminogens, tetraarylethylenes attract considerable attentions due to their widespread applications in chemo‐/biosensing and optoelectronic devices. The structural diversity of tetraarylethylenes constructs a powerful platform for exploring their distinguished high‐tech applications. A variety of synthetic protocols for the preparation of stereodefined tetraarylethylenes are summarized, and differences in properties and applications of TAEs stereoisomers are also discussed. |
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ISSN: | 2692-4560 2692-4560 |