Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/33768
Title: Synthesis of zinc porphyrins and effect of peripheral substituents on the coordination reaction
Authors: Wang, Shujun
Peng, Yuling
Zhang, Chenggen
Li, Yongbing
Liu, Chao
Keywords: Coordination chemistry;Theoretical chemistry;Porphyrins;Zinc porphyrins;UV-visible spectroscopy;Fluorescence quenching
Issue Date: Feb-2016
Publisher: NISCAIR-CSIR, India
Abstract: Three free-base porphyrins, modified with Boc-D-threonine and their zinc porphyrins have been synthesized using benzaldehyde, 4-chlorobenzaldehyde, and 4-methoxybenzaldehyde. The effects of peripheral substituents on the coordination reactions between zinc porphyrins and imidazole derivatives have been studied by UV-visible spectroscopy, fluorescence spectrometry, and theoretical calculations. The results show that the coordination reaction forms a Zn-N bond between zinc porphyrins involving different peripheral substituents and imidazole derivatives. The association coordination constants decrease (N-MeIm > Im) due to the change in enthalpy; the zinc porphyrin synthesized using 4-chlorobenzaldehyde and N-methylimidazole shows the largest association constant. Fluorescent quenching is observed during the coordination process with the zinc porphyrin synthesized using 4-methoxybenzaldehyde and N-methylimidazole showing the largest Stern-Volmer quenching rate constant. In addition, theoretical calculations have been used to investigate essential characteristics of the reaction, charges, bond lengths, and bond energies for each system.
Page(s): 145-152
URI: http://hdl.handle.net/123456789/33768
ISSN: 0975-0975(Online); 0376-4710(Print)
Appears in Collections:IJC-A Vol.55A(02) [February 2016]

Files in This Item:
File Description SizeFormat 
IJCA 55A(2) 145-152.pdf550.17 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.