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含9-丁基咔唑基二炔/聚炔汞及二炔金配合物的合成与性质

柳利1,2; 陈祖兴1; 柳士忠1; 黄维扬2   

  1. 1. 湖北大学化学化工学院,有机功能分子合成与应用教育部重点实验室, 武汉 430062;
    2. 香港浸会大学化学系, 香港
  • 收稿日期:2005-10-18 修回日期:1900-01-01 出版日期:2006-07-10 发布日期:2006-07-10
  • 通讯作者: 黄维扬

Synthesis and Properties of Hg Diyne/Poly-yne and Au Diyne
Complexes Containing 9-Butylcarbazole Unit

LIU Li1,2; CHEN Zu-Xing1; LIU Shi-Zhong1; WONG Wai-Yeung2*   

  1. 1. Key Laboratory for the Synthesis and Application of Organic Function Moleculs,
    Ministry of Education, Faculty of Chemistry and Chemical Engineering, Hubei
    University, Wuhan 430062, China;
    2. Department of Chemistry, Hong Kong Baptist University, Hong Kong, China
  • Received:2005-10-18 Revised:1900-01-01 Online:2006-07-10 Published:2006-07-10
  • Contact: HUANG Wei-Yang

摘要: 合成了9-丁基咔唑基聚炔汞聚合物[—HgC≡CRC≡C—]n及其二聚体[MeHgC≡CRC≡CHgMe]和金的二聚体[(PPh3)AuC≡CRC≡CAu(PPh3)](R=9-丁基咔唑基). 用 1H NMR, 13C NMR, 31P NMR, FTIR, FAB-MS, UV-Vis, Fluorescence及Phosphorescence 光谱对其进行了表征. 结果表明, 体系中金和汞产生的重原子效应可以促进单线激发态S1与三线激发态T1的系间跃迁, 使标题化合物产生有机三线态发光.

关键词: 9-丁基咔唑基聚炔汞, 二炔金配合物, 合成, 荧光, 磷光

Abstract: Three new d10 Hg and Au poly-yne and its diyne containing 9-butylcarbazole unit were synthesized by dehydrohalogenation reactions and characterized by 1H NMR, 13C NMR, 31P NMR, FTIR, FAB-MS, UV-Vis, fluorescence and phosphorescence spectroscopies. All the compounds were analytically and spectroscopically characterized to possess a well-defined size and structure. The materials are organic\|soluble and solution-processable. The results show that the organic triplet emission can be harvested by the heavy-atom effect induced by Au and Hg which can efficiently promote the intersystem transition from the S1 singlet excited state to the T1 triplet excited state. The relationship between the T1 energy state and the intersystem transition for the system was discussed. It is envisioned that a structure\|property\|function relationship can be established and valuable insight into the photophysical nature of conjugated materials can be subsequently derived.

Key words: 9-Butylcarbazole polyyne, Gold diyne complex, Synthesis, Fluorescence, Phosphorescence

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