Department of Chemistry and Biochemistry, Graduate School of Engineering, Kyushu University, 744 Moto-oka, Nishi-ku, Fukuoka 819-0395, Japan.
Inorg Chem. 2013 Aug 19;52(16):9613-9. doi: 10.1021/ic401314a. Epub 2013 Aug 5.
Three possible isomers of N-fused tetraphenylporphyrin ruthenium complexes, Ru(NFTPp)Cl(CO)2 (2a-c), were isolated and fully characterized by NMR, IR, CV, UV-vis-NIR absorption, and X-ray crystallographic analyses. Each isomer was stable at ambient conditions and isomerization among 2a-c occurred at elevated temperature both in solution and in a solid state, through the intramolecular rotational pathways. Electronic structures of 2a-c were analyzed in detail by DFT study to reveal appreciable differences in the interaction between the NFTPp ligand and the Ru-Cl moiety.
三种可能的 N-稠合四苯基卟啉钌配合物异构体 Ru(NFTPp)Cl(CO)2 (2a-c) 被分离并通过 NMR、IR、CV、UV-vis-NIR 吸收和 X 射线晶体学分析进行了全面表征。每种异构体在环境条件下都是稳定的,2a-c 之间的异构化在溶液中和固态中均在升高的温度下通过分子内旋转途径发生。通过 DFT 研究详细分析了 2a-c 的电子结构,以揭示 NFTPp 配体与 Ru-Cl 部分之间相互作用的显著差异。