高等学校化学学报2024,Vol.45Issue(1) :160-165.DOI:10.7503/cjcu20230432

一锅法合成可印刷室温磷光二氟化硼衍生物

One-pot Synthesis of Room Temperature Phosphorescent Boron-difluoride Derivative for Printing

张兴红 耿鹏 向娟娟 晏佳莹 毛妙付 肖述章
高等学校化学学报2024,Vol.45Issue(1) :160-165.DOI:10.7503/cjcu20230432

一锅法合成可印刷室温磷光二氟化硼衍生物

One-pot Synthesis of Room Temperature Phosphorescent Boron-difluoride Derivative for Printing

张兴红 1耿鹏 1向娟娟 1晏佳莹 1毛妙付 1肖述章1
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作者信息

  • 1. 三峡大学材料与化工学院,宜昌 443002
  • 折叠

摘要

纯有机室温磷光(RTP)材料因其潜在的应用价值而备受关注.迄今,多数已报道的有机RTP材料在晶态下发射出较强的RTP,但在溶液加工过程中易生成无定形态,从而失去RTP性能.本文通过一锅法两步反应,合成了含有多个甲氧基的二氟化硼衍生物(BF2-tPMO).晶体结构分析表明,多个甲氧基的存在构建了有效的分子间非共价相互作用.这些非共价键作用可抑制分子运动,保持较高的发光效率.此外,这些非共价键作用能够使其在溶剂处理后依然保持晶态性质,进而保持RTP性能.实验结果表明,BF2-tPMO可溶解在不同溶剂中且在溶剂蒸发后仍能保持相同的RTP特性,为易加工型RTP材料的设计提供了有效的策略.

Abstract

Pure organic room-temperature phosphorescent(RTP)materials have been under wide investigation due to their various potential applications.Till now,most reported organic RTP materials emit robust RTP in crystalline state,but lose RTP properties during the solution processing.Here,a boron-difluoride derivative bearing multiple methoxy group(BF2-tPMO)was synthesized through a one-pot two-step reaction.The existence of multiple methoxy groups helped to construct effective intermolecular non-covalent interactions,as revealed by X-ray single crystal structure.These intermolecular non-covalent interactions might help to alleviate molecular motions to increase emission efficiency,and also help to maintain its crystalline nature during the evaporation of organic solutions to keep its RTP character.Our experimental results indicate that BF2-tPMO maintained its RTP properties after solution processing,providing an effective strategy for designing RTP materials with convenient manipulation.

关键词

二氟化硼/室温磷光/一锅法合成/分子间相互作用

Key words

Boron-difluoride/Room temperature phosphorescence/One-pot synthesis/Intermolecular interaction

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基金项目

国家自然科学基金(22171163)

三峡大学高等学校学科创新引智计划(111引智计划)(D20015)

宜昌市自然科学基金(A23-2-025)

出版年

2024
高等学校化学学报
中华人民共和国教育部委托 吉林大学和南开大学

高等学校化学学报

CSTPCDCSCD北大核心
影响因子:1.067
ISSN:0251-0790
参考文献量35
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