Determination of double decker sandwich structured la-substituted chlorophyll a by EXAFS
Document Type
Article
Publication Date
12-1-2000
Abstract
Double decker sandwich lanthanoid porphyrins have been synthesized and characterized systematically. Chlorophyll is a representative of natural porphyrin derivatives. It is therefore interesting to study the chemical form of lanthanide in chlorophyll. We synthesized Lanthanum (III) Chlorophyll a derivatives, whose UV-vis and IR spectra confirm the coordination of La(III) to the porphyrin rings. MCD spectra show the special bands in Soret band region, which indicate a transition from sandwich structure porphyrin complexes. By extended X-ray absorption fine structure (EXAFS) method, it is found that the molecular structure of synthesized La-Chla can be well fitted by the double decker sandwich structure model that La is surrounded by eight nitrogen atoms from two porphyrin rings. The MCD and EXAFS results indicate that the La in chlorophyll a exist as a sandwich shaped complexes with an average La-N bond length of 0.261nm. To our best knowledge, this is the first example of La-Chla with a double decker sandwich molecular structure.
Publication Source (Journal or Book title)
Acta Chimica Sinica
First Page
559
Last Page
562
Recommended Citation
Wei, Z., Hong, F., Zhao, G., Tao, Y., Hu, T., Liu, T., Xie, Y., Yin, M., Li, B., & Yang, J. (2000). Determination of double decker sandwich structured la-substituted chlorophyll a by EXAFS. Acta Chimica Sinica, 58 (5), 559-562. Retrieved from https://repository.lsu.edu/ag_exst_pubs/1084