Affiliation:
1. College of Environment and Resources Engineering Research Center of Polymer Green Recycling of Ministry of Education Fujian Key Laboratory of Pollution Control &Resource Reuse Fujian Normal University Fuzhou 350007 China
2. Key Laboratory of Coal to Ethylene Glycol and Its Related Technology, State Key Laboratory of Structural Chemistry Center for Excellence in Molecular Synthesis, Fujian Institute of Research on the Structure of Matter Chinese Academy of Sciences Fuzhou 350002 China
3. College of Chemistry Fuzhou University Fuzhou 350108 China
Abstract
AbstractThe properties of polyethylene are highly dependent on the variety and quantity of substitutions. Generally, polyethylene can only be fully substituted with fluorine atoms, mainly e. g., polytetrafluoroethylene and nafion, because atomic radius of fluorine atom is small enough. The preparation of fully substituted polyethylene analogues (FSPEA) and their non‐traditional intrinsic luminescence (NTIL) are attractive, especially for substitutions with relatively larger atomic radii than a fluorine atom. Here, Barbier polymerization‐induced emission (PIE) is demonstrated as a universal method for the molecular design of NTIL type FSPEAs with intriguing aggregation‐induced emission (AIE) behaviors. Through Barbier polymerization of diphenyldichloromethane and different peroxyesters in the presence of Mg in one pot, a series of FSPEAs, including polytriphenylethanol (PTPE), polydiphenylfurylethanol (PDPFE), polydiphenylthiophenylethanol (PDPTE) and polydiphenylnaphthylethanol (PDPNE) have been successfully prepared. Further potential applications for explosive detection, artificial light‐harvesting system and white phosphor‐converted light‐emitting diode are investigated. Therefore, this work opens up a new approach for the molecular design of FSPEA with non‐conjugated luminescence, which may cause inspirations to different research fields like polyolefin and luminescent materials.
Funder
National Natural Science Foundation of China
Subject
General Chemistry,Catalysis,Organic Chemistry
Cited by
2 articles.
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