Synthesis, Characterization, Spectroelectrochemical, Photophysical and HSA-Binding Properties of Novel and Versatile meso-Tetra(4-pyridylvinylphenyl)porphyrins Coordinated to Ruthenium(II)-Polypyridyl Derivatives

被引:8
|
作者
Viecelli, Viviane [1 ]
Chaves, Otavio A. [2 ]
Araki, Koiti [3 ]
Martins, Paulo R. [4 ]
Iglesias, Bernardo A. [1 ]
机构
[1] Univ Fed Santa Maria, Lab Bioinorgan & Mat Porfirin, Dept Quim, Av Roraima 1000, BR-97105900 Santa Maria, RS, Brazil
[2] Inst SENAI Inovacao Quim Verde, Rua Morais & Silva 53, BR-20271030 Rio De Janeiro, RJ, Brazil
[3] Univ Sao Paulo, Inst Quim, Av Prof Lineu Prestes 748, BR-05508000 Sao Paulo, SP, Brazil
[4] Univ Fed Goias, Inst Quim, Av Esperanca S-N, BR-74690900 Goiania, Go, Brazil
基金
巴西圣保罗研究基金会;
关键词
porphyrins; ruthenium(II) complexes; electrocatalysis; singlet oxygen; HSA-binding; PORPHYRIN; DNA; METALLOPORPHYRINS; COMPLEXES;
D O I
10.21577/0103-5053.20200080
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The free-base meso-tetra(4-pyridylvinylphenyl)porphyrin (1a) and its zinc(II) complex were synthesized and then functionalized with [Ru(bpy)(2)Cl](+) units (2a and 2b) via conventional methods and evaluated in terms of photophysical, electrochemical and biological aspects. All porphyrins present moderate singlet oxygen production and fluorescence quantum yield, and did not show any aggregation process. The photo-oxidation ability of those porphyrins decreased in the order 2b > 1a > 2a. The electrochemical behavior of 2a and 2b modified electrodes was evaluated by electroanalytical methods. Also the 2b electrode showed a smaller charge transfer resistance (36.70 Omega) when compared to 2a electrode (45.17 Omega). In addition, even after 30 consecutive injections of nitrite solution (1.0 x 10(-4) mol L-1) using the flow injection analysis (FIA) system, the modified 2b electrode showed an relative standard deviation (RSD, n = 30) of 1.36% exhibiting a great potential as amperometric sensor for nitrite. Moreover, the biological evaluation towards human serum albumin (HSA) indicated spontaneous, weak and ground-state association in the IB subdomain (site III) and possibily a second site, changing the conventional interaction mode of porphyrins with biomolecules as consequence of the longer arms (porphyrin ring substituents at meso-positions) ending with a ruthenium polypyridyl complex, that may enhance the photodynamic therapy (PDT) efficiency of photogenerated reactive oxygen species (ROS) species.
引用
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页码:2282 / 2298
页数:17
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