Development of Functional Molecules Based on Ring-Fusion Strategy

基于环融合策略的功能分子开发

• 批准号: 21750047
• 负责人: TOGANOH Motoki
• 金额: $ 2.91万
• 依托单位: Kyushu University
• 依托单位国家: 日本
• 项目类别: Grant-in-Aid for Young Scientists (B)
• 财政年份: 2009
• 资助国家: 日本
• 起止时间: 2009 至 2011
• 项目状态: 已结题
• 来源: https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-21750047/
• 关键词: ポルフィリン; 近赤外線素子; マンガン錯体; 異性体; フェロセン; コロール; 有機近赤外素子; 近赤外色素; 遷移金属錯体; π共役系; DFT計算

A variety of N-fused porphyrin derivatives were synthesized by the ring-fusion strategy and their photophysical properties were investigated. Observed near infrared fluorescence would be derived from excited-state intramolecular proton transfer. In addition, larger two-photon absorption cross sections were observed in the N-fused porphyrin derivatives. Meanwhile, double-decker iron(II) complex of N-fused porphyrinato was successfully synthesized, having unique three-dimensional d-Π conjugated system. These results clearly illustrated the effectiveness of ring-fusion strategy in study of near infrared dyes.

采用环融合策略合成了多种n -熔融卟啉衍生物，并对其光物理性质进行了研究。观察到的近红外荧光来源于激发态的分子内质子转移。此外，在n -熔融卟啉衍生物中观察到较大的双光子吸收截面。同时，成功合成了双层n -熔融卟啉铁（II）配合物，具有独特的三维d-Π共轭体系。这些结果清楚地说明了环融合策略在近红外染料研究中的有效性。