¹H NMR and HPLC studies of tetraarylporphyrin atropisomers

• Main Author: Shi, Yunqing Nancy
• Format: Others
• Published: Scholarly Commons 1993
• Subjects: Porphyrins; Chemical tests and reagents; High performance liquid chromatography; Lanthanide shift reagents; Physical Sciences and Mathematics
• Online Access: https://scholarlycommons.pacific.edu/uop_etds/2250; https://scholarlycommons.pacific.edu/cgi/viewcontent.cgi?article=3249&context=uop_etds

This thesis includes NMR studies of free base meso-tetra(otolyl) porphyrin (TTP) and meso -tetraphenylporphyrin (TPP) and their dications protonated by trifluoroacetic acid (TFA). The chemical shift changes of the -NH resonance are very unusual and have never been reported. At the beginning of the titration, the N-H resonances broaden considerably but do not shift; when the ratio of [TFA]/[TTP] or [TFA]/[TPPf are over 2, the N-H resonances shift markedly to lower field by as much as 1.6 ppm. At acid levels well above the equivalence point, the NH resonances moves back to higher field. Moreover upon protonation the NH line of TTP becomes a complex multiplet which changes as a function of [TFA]/[TTP]. The NH line of TPP remains a singlet at all acid levels. We also report here a way of isolating atropisomers of mesotetra( o -tolyl)porphyrin through HPLC by using an analytical C-18 bond pack reverse phase column eluted by a 1 %THF + 99%Me0H solvent combination. A preliminary study by HPLC was also carried out on ZnTTP(II) with aliquots of 2,6-dimethylpyridine, and the retention time of the separation decreased markedly, but this study needs to be repeated and improved. TTP and TPP dications at two different acid levels were studied by VT-NMR, and the downfield shift of -NH resonance of TTP dications was more pronounced at higher temperatures than those of TPP dications.