Hypervalent Phosphorus(V) Porphyrins with meso-Methoxyphenyl Substituents: Significance of the Number and Position of Methoxy Groups in Promoting Intramolecular Charge Transfer

• Published in: Inorganic chemistry 2022-10, Vol.61 (42), p.16573-16585
• Main Authors: Sharma, Jatan K., Bayard, Brandon J., Zosel, Nick, Ali, Syeda S., Holzer, Noah, Nesterov, Vladimir N., Karr, Paul A., D’Souza, Francis, Poddutoori, Prashanth K.
• Format: Article
• Language: English
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.2c01648

To study the photophysical and redox properties as a function of meso-aryl units, a series of hypervalent phosphorus­(V) porphyrins, PP­(OMe)2·PF6, PMP­(OMe)2·PF6, PDMP­(OMe)2·PF6, P345TMP­(OMe)2·PF6, and P246TMP­(OMe)2·PF6, with phenyl (P), 4-methoxyphenyl (MP), 3,5-dimethoxyphenyl (DMP), 3,4,5-trimethoxyphenyl (345TMP), and 2,4,6-trimethoxyphenyl (246TMP) units, respectively, have been synthesized. The P­(+5) in the cavity makes the porphyrin ring electron-poor, whereas the methoxy groups make the meso-phenyl rings electron-rich. The presence of electron-rich and electron-poor portions within the porphyrin molecule promoted an intramolecular charge transfer (ICT). Also, the study suggests that the ICT depends on the number and position of the methoxy groups. The ICT is more prominent in m-methoxy-substituted phosphorus­(V) porphyrins (PDMP­(OMe)2.PF6, P345TMP­(OMe)2·PF6) and almost no ICT was found in no-methoxy, o-methoxy, and/or p-methoxy phosphorus­(V) porphyrins (PP­(OMe)2·PF6, PMP­(OMe)2·PF6, P246TMP­(OMe)2·PF6). Transient absorption studies indicate that the ICT takes place on the picosecond time scale. The most striking results come from P246TMP­(OMe)2·PF6, where each phenyl ring carries three methoxy units, like the P345TMP­(OMe)2·PF6, but it failed to induce the ICT process. Electrochemical studies and time-dependent density functional theory (TD-DFT) calculations were used to support the experimental results. This study extensively explores why and how slight variations in meso-aryl substitutions lead to intricate changes in the photophysical and redox properties of phosphorus­(V) porphyrins.