Electronic investigation of light-induced reversible coordination of Co(II)/spiropyran complex

被引:25
作者
Miguez, Flavio B. [1 ]
Reis, Izadora F. [1 ]
Dutra, Lucas P. [2 ]
Silva, Igor M. S. [3 ]
Verano-Brag, Thiago [3 ]
Lopes, Juliana Fedoce [2 ]
De Sousa, Frederico B. [1 ]
机构
[1] Univ Fed Itajuba UNIFEI, Inst Fis & Quim, LSPS, BR-37500903 Itajuba, MG, Brazil
[2] Univ Fed Itajuba UNIFEI, Inst Fis & Quim, Lab Quim Computac LaQC, BR-37500903 Itajuba, MG, Brazil
[3] Univ Fed Minas Gerais, Dept Fisiol & Biofis, Inst Ciencias Biol, BR-31270901 Belo Horizonte, MG, Brazil
关键词
Spiropyran; Coordination complex; Chromism; Density functional theory; Electronic structure; SPIROPYRAN; PHOTO; LIGANDS; BINDING;
D O I
10.1016/j.dyepig.2019.107757
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Herein, synthesis and characterization of a cobalt (II) complex using a spiropyran as its ligand was described. Solid complex (CoMC) was obtained using a novel ultraviolet radiation-induced precipitation technique, FTIR-ATR spectroscopy demonstrated the binding sites involved in the coordination. Computational calculations were crucial to understand the experimental results, demonstrating the frontiers orbitals in tetrahydrofuran. Moreover, mass spectrometry revealed a 1:2 Co(II)ligand stoichiometry. By means of UV-vis absorption spectroscopy, complexation was confirmed and photochromic and the solvatochromic characteristics of the complex and the free ligand were studied. These results showed that the complex did not present a would be expected pattern regarding its solvatochromic properties, while the free ligand did. Reversibility experiments exposed a high resistance to photodegradation of the complex in isopropanol, comparing to the other solvents tested.
引用
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页数:7
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