Complexation of Zn Arylporphyrinates with Leucine Methyl Ester
摘要:
Extra coordination of L-leucine methyl ester with seventeen different Zn arylporphyrinates is studied by spectrophotometric titration and capability of Zn porphyrinates with the active OH groups to recognize LeiOCH(3) in toluene at 20degreesC is determined. The formation of associates of the composition amino acid etherporphyrinate depending on the substituent positions in a macrocycle is studied by the H-1 NMR method. The most strong donor-acceptor bonds between Zn porphyrinate and LeiOCH(3) are observed in the case of pyridine-substituted porphyrins and porphyrins with phenyl rings containing electron-donor substituents in the m-position. The best recognizing capabilities with respect to leucine are shown by Zn porphyrinates with di- and tetra-4-OH-phenyl substitution in the meso-positions of a macrocycle.