Volume 57, Issue 21
Communication

Tunable Multicolor Phosphorescence of Crystalline Polymeric Complex Salts with Metallophilic Backbones

Qi Liu

Technical Institute of Physics and Chemistry & University of, Chinese Academy of Sciences, Beijing, 100190 P. R. China

Department of Chemistry, South University of Science and Technology of China, Shenzhen, Guangdong, 518055 P. R. China

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Dr. Mo Xie

Department of Chemistry, South University of Science and Technology of China, Shenzhen, Guangdong, 518055 P. R. China

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Dr. Xiaoyong Chang

Department of Chemistry, South University of Science and Technology of China, Shenzhen, Guangdong, 518055 P. R. China

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Dr. Shuang Cao

Technical Institute of Physics and Chemistry & University of, Chinese Academy of Sciences, Beijing, 100190 P. R. China

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Dr. Chao Zou

Department of Chemistry, South University of Science and Technology of China, Shenzhen, Guangdong, 518055 P. R. China

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Prof. Dr. Wen‐Fu Fu

Technical Institute of Physics and Chemistry & University of, Chinese Academy of Sciences, Beijing, 100190 P. R. China

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Prof. Dr. Chi‐Ming Che

State Key Laboratory of Synthetic Chemistry and Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, P. R. China

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Prof. Dr. Yong Chen

Corresponding Author

E-mail address: chenyong@mail.ipc.ac.cn

Technical Institute of Physics and Chemistry & University of, Chinese Academy of Sciences, Beijing, 100190 P. R. China

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Prof. Dr. Wei Lu

Corresponding Author

E-mail address: luw@sustc.edu.cn

Department of Chemistry, South University of Science and Technology of China, Shenzhen, Guangdong, 518055 P. R. China

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First published: 14 April 2018
Citations: 17

Abstract

A total of 35 [Au(NHC)2][MX2] (NHC=N‐heterocyclic carbene; M=Au or Cu; X=halide, cyanide or arylacetylide) complex salts were synthesized by co‐precipitation of [Au(NHC)2]+ cations and [MX2] anions. These salts contain crystallographically determined polymeric Au⋅⋅⋅Au or Au⋅⋅⋅Cu interactions and are highly phosphorescent with quantum yields up to unity and emission color tunable in the entire visible regions. The nature of the emissive excited states is generally assigned to ligand (anion)‐to‐ligand (cation) charge‐transfer transitions assisted by d10⋅⋅⋅d10 metallophilicity. The emission properties can be further tuned by controlled triple‐component co‐crystallization or by epitaxial growth. Correct recipes for white light‐emitting phosphors with quantum yields higher than 70 % have been achieved by screening the combinatorial pool.

Number of times cited according to CrossRef: 17

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