Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2017:2017:6426747.
doi: 10.1155/2017/6426747. Epub 2017 Feb 7.

Synthesis Characterization and Biological Activities of Coordination Compounds of 4-Hydroxy-3-nitro-2 H-chromen-2-one and Its Aminoethanoic Acid and Pyrrolidine-2-carboxylic Acid Mixed Ligand Complexes

Affiliations

Synthesis Characterization and Biological Activities of Coordination Compounds of 4-Hydroxy-3-nitro-2 H-chromen-2-one and Its Aminoethanoic Acid and Pyrrolidine-2-carboxylic Acid Mixed Ligand Complexes

Temitayo Aiyelabola et al. Bioinorg Chem Appl. 2017.

Abstract

Coordination compounds of 4-hydroxy-3-nitro-2H-chromen-2-one and their mixed ligand complexes with aminoethanoic acid and pyrrolidine-2-carboxylic acid were synthesized by the reaction of Cu(II) and Zn(II) salts in molar ratio 1 : 2 for the coumarin complexes and 1 : 1 : 1 for the mixed ligand complexes, in basic media. The compounds formed were characterized using infrared, Uv-vis spectrophotometric analyses, mass spectrometry, magnetic susceptibility measurements, and EDX analyses. It was concluded that 4-hydroxy-3-nitro-2H-chromen-2-one coordinated as a monobasic ligand for all the complexes; it also coordinated via the carbonyl moiety in the case of the Cu(II) mixed ligand complexes. Similarly it was proposed that the amino acids also coordinated in a bidentate fashion via their amino nitrogen and carboxylate oxygen atoms. The synthesized compounds were screened for their antimicrobial and cytotoxic activities. The complexes exhibited marginal antimicrobial activity but good cytotoxic activity.

PubMed Disclaimer

Conflict of interest statement

The authors declare that there are no competing interests regarding the publication of this paper.

Figures

Figure 1
Figure 1
Structures of the ligands.
Figure 2
Figure 2
Proposed structure for compounds 1 and 2.
Figure 3
Figure 3
Proposed structure for compounds 3 and 5. R=–H, compound 3, and –C4H8, compound 5.
Figure 4
Figure 4
Proposed structure for compounds 4 and 6. R=–H, compound 4, and –C4H8, compound 6.

References

    1. Bahekar S. S., Shinde D. B. Samarium(III) catalyzed one-pot construction of coumarins. Tetrahedron Letters. 2004;45(43):7999–8001. doi: 10.1016/j.tetlet.2004.09.013. - DOI
    1. Emmanuel-Giota A. A., Fylaktakidou K. C. Synthesis and biological evaluation of several 3-(coumarin-4-yl)tetrahydroisoxazole and 3-(coumarin-4-yl)dihydropyrazole derivatives. Journal of Heterocyclic Chemistry. 2001;38(3):717–722. doi: 10.1002/jhet.5570380329. - DOI
    1. El-Sayed A. M., Abd Allah O. A. Synthetic and biological studies on coumarin hydrazone derivatives. Phosphorus, Sulfur and Silicon and Related Elements. 2001;170:75–86. doi: 10.1080/10426500108040586. - DOI
    1. Raev L. D., Voinova E., Ivanov I. C., Popov D. Antitumor activity of some coumarin derivatives. Pharmazie. 1990;45(9):p. 696. - PubMed
    1. Karaliota A., Kretsi O., Tzougraki C. Synthesis and characterization of a binuclear coumarin-3-carboxylate copper(II) complex. Journal of Inorganic Biochemistry. 2001;84(1-2):33–37. doi: 10.1016/S0162-0134(00)00214-2. - DOI - PubMed

LinkOut - more resources