Studies on Zn(II) monohydroxyphenyl mesoporphyrinic complexes. Synthesis and characterization

被引:17
作者
Boscencu, Rica [1 ]
Socoteanu, Radu [2 ]
Oliveira, Anabela S. [3 ]
Ferreira, Luis Filipe Vieira [3 ]
机构
[1] Carol Davila Univ Med & Pharm, Fac Pharm, Dept Inorgan Chem, Bucharest, Romania
[2] Acad Romana, Inst Phys Chem IG Murgulescu, Bucharest 77208, Romania
[3] Univ Tecn Lisboa, Inst Super Tecn, Ctr Quim Fis Mol, P-1049001 Lisbon, Portugal
关键词
asymmetric porphyrins; Zn(II) porphyrin complexes; sensitizers for photodynamic therapy; molecular absorption coefficients; NMR spectroscopy;
D O I
10.2298/JSC0807713B
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of four Zn(II) complexes with asymmetrical porphyrinic ligands were synthesized: [5-(4-hydroxyphenyl)-10,15,20-triphenyl-21H,23H-porphinato]Zn(II) (Zn(II)TPPOHP), [5-(3-hydroxyphenyl)-10,15,20-triphenyl-21H,23H-porphinato]Zn(II) (Zn(II)TPPOHM), [5-(2-hydroxyphenyl)-10,15,20-triphenyl-21H,23H-Zn(II)-porphinato]Zn(II) (Zn(II)TPPOHO) and the well-known (5,10,15,20-tetraphenyl-21H,23H-porphinato]Zn(II) (Zn(II)TPP) as reference, in a 1:1 mole ratio. In all cases, the free-base porphyrin served as a tetradentate ligand through the four pyrrole nitrogen atoms. The complexes were characterized by elemental analysis, FTIR and UV-Vis spectroscopy, which fully confirmed the structure of the complexes. UV-Vis showed that the spectral absorption of the four complexes was blue-shifted by at least 50 nm compared to that of the free ligands. Also important structural data were obtained from several different NMR experiments (including H-1-NMR, C-13-NMR, DEPT, COSY, HMBC and HMQC). Influences of external substituents on the porphyrin ring were observed.
引用
收藏
页码:713 / 726
页数:14
相关论文
共 43 条
[1]   Photosensitizers in clinical PDT [J].
Allison, Ron R. ;
Downie, Gordon H. ;
Cuenca, Rosa ;
Hu, Xin-Hua ;
Childs, Carter J. H. ;
Sibata, Claudio H. .
PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY, 2004, 1 (01) :27-42
[2]   Singlet oxygen generation using iodinated squaraine and squaraine-rotaxane dyes [J].
Arunkumar, Easwaran ;
Sudeep, Pallikkara K. ;
Kamat, Prashant V. ;
Noll, Bruce C. ;
Smith, Bradley D. .
NEW JOURNAL OF CHEMISTRY, 2007, 31 (05) :677-683
[3]  
Bonnett Alastair., 2000, ANTIRACISM
[4]  
Boscencu R, 2008, POL J CHEM, V82, P509
[5]  
Boscencu R, 2003, REV CHIM-BUCHAREST, V54, P256
[6]  
Boscencu R, 2002, REV CHIM-BUCHAREST, V53, P619
[7]  
Boscencu R, 2007, REV CHIM-BUCHAREST, V58, P498
[8]   Structure and biodistribution relationships of photodynamic sensitizers [J].
Boyle, RW ;
Dolphin, D .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1996, 64 (03) :469-485
[9]  
Buchler J.W., 1975, PORPHYRINS METALLOPO, P157
[10]   Photodynamic therapy [J].
Dougherty, TJ ;
Gomer, CJ ;
Henderson, BW ;
Jori, G ;
Kessel, D ;
Korbelik, M ;
Moan, J ;
Peng, Q .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (12) :889-905