Synthesis and structure of new tetracopper(II) complexes bridged by 2-{N′-[2-(dimethylamino)ethyl]oxamido}benzoate: DNA-binding and anticancer activity

Tetranuclear complexes constructed from asymmetrical N,N′-bis(substituted)oxamide have been synthesized and characterized by X-ray single-crystal diffraction. The cytotoxicities and reactivities towards DNA of the two complexes have been investigated. [Display omitted] ► Two tetranuclear complexes h...

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Published inJournal of photochemistry and photobiology. B, Biology Vol. 114; pp. 27 - 37
Main Authors Zheng, Yong-Jun, Li, Xiao-Wen, Li, Yan-Tuan, Wu, Zhi-Yong, Yan, Cui-Wei
Format Journal Article
LanguageEnglish
Published Switzerland Elsevier B.V 03.09.2012
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Online AccessGet full text
ISSN1011-1344
1873-2682
1873-2682
DOI10.1016/j.jphotobiol.2012.05.004

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Abstract Tetranuclear complexes constructed from asymmetrical N,N′-bis(substituted)oxamide have been synthesized and characterized by X-ray single-crystal diffraction. The cytotoxicities and reactivities towards DNA of the two complexes have been investigated. [Display omitted] ► Two tetranuclear complexes have been synthesized and characterized. ► The two complexes exhibit cytotoxicities against SMMC-7721 and A549 cell lines. ► The DNA-binding abilities are consistent with cytotoxicities in the order 2>1. ► The terminal ligands are very important in the DNA-binding and cytotoxic properties. Two new circular tetranuclear copper(II) complexes, [Cu4(dmoxba)2(bpy)2(CH3OH)2](pic)2·2H2O (1) and [Cu4(dmoxba)2(phen)2](pic)2·2CH3OH (2), where dmoxba, pic, bpy and phen stand for the anion of 2-{N′-[2-(dimethylamino)ethyl]oxamido}benzoate, picrate, 2,2′-bipyridine and 1,10-phenanthroline, respectively, have been synthesized and structurally characterized by X-ray single-crystal diffraction. Both the complexes have embedded inversion centers and similar complex cations assembled by the oxamide-bridges and carboxylate-bridges of two cis-dmoxba3− ligands. The Cu⋯Cu separations through the oxamide-bridge and the carboxylato-bridge are 5.1991(4) and 5.4674(4)Å in 1 and 5.1843(5) and 5.2138(5)Å in 2, respectively. Both copper(II) ions are in square-pyramidal environments in 1. While in complex 2, the inner and exo copper(II) ions have square-planar and square-pyramidal coordination geometries, respectively. In both the crystals, three-dimensional supramolecular structures are formed by hydrogen bonds and π–π stacking interactions. The DNA-binding properties and anticancer activities of the two complexes were investigated. The results suggest that the two complexes interact with HS-DNA in the mode of intercalation with the intrinsic binding constants 5.0×104M−1 (1) and 6.7×104M−1 (2). The influence of structural variation of the terminal ligands in the tetranuclear complexes on DNA-binding properties is preliminarily discussed.
AbstractList Two new circular tetranuclear copper(II) complexes, [Cu₄(dmoxba)₂(bpy)₂(CH₃OH)₂](pic)₂·2H₂O (1) and [Cu₄(dmoxba)₂(phen)₂](pic)₂·2CH₃OH (2), where dmoxba, pic, bpy and phen stand for the anion of 2-{N′-[2-(dimethylamino)ethyl]oxamido}benzoate, picrate, 2,2′-bipyridine and 1,10-phenanthroline, respectively, have been synthesized and structurally characterized by X-ray single-crystal diffraction. Both the complexes have embedded inversion centers and similar complex cations assembled by the oxamide-bridges and carboxylate-bridges of two cis-dmoxba³⁻ ligands. The Cu⋯Cu separations through the oxamide-bridge and the carboxylato-bridge are 5.1991(4) and 5.4674(4)Å in 1 and 5.1843(5) and 5.2138(5)Å in 2, respectively. Both copper(II) ions are in square-pyramidal environments in 1. While in complex 2, the inner and exo copper(II) ions have square-planar and square-pyramidal coordination geometries, respectively. In both the crystals, three-dimensional supramolecular structures are formed by hydrogen bonds and π–π stacking interactions. The DNA-binding properties and anticancer activities of the two complexes were investigated. The results suggest that the two complexes interact with HS-DNA in the mode of intercalation with the intrinsic binding constants 5.0×10⁴M⁻¹ (1) and 6.7×10⁴M⁻¹ (2). The influence of structural variation of the terminal ligands in the tetranuclear complexes on DNA-binding properties is preliminarily discussed.
Two new circular tetranuclear copper(II) complexes, [Cu(4)(dmoxba)(2)(bpy)(2)(CH(3)OH)(2)](pic)(2)·2H(2)O (1) and [Cu(4)(dmoxba)(2)(phen)(2)](pic)(2)·2CH(3)OH (2), where dmoxba, pic, bpy and phen stand for the anion of 2-{N'-[2-(dimethylamino)ethyl]oxamido}benzoate, picrate, 2,2'-bipyridine and 1,10-phenanthroline, respectively, have been synthesized and structurally characterized by X-ray single-crystal diffraction. Both the complexes have embedded inversion centers and similar complex cations assembled by the oxamide-bridges and carboxylate-bridges of two cis-dmoxba(3-) ligands. The Cu···Cu separations through the oxamide-bridge and the carboxylato-bridge are 5.1991(4) and 5.4674(4) Å in 1 and 5.1843(5) and 5.2138(5) Å in 2, respectively. Both copper(II) ions are in square-pyramidal environments in 1. While in complex 2, the inner and exo copper(II) ions have square-planar and square-pyramidal coordination geometries, respectively. In both the crystals, three-dimensional supramolecular structures are formed by hydrogen bonds and π-π stacking interactions. The DNA-binding properties and anticancer activities of the two complexes were investigated. The results suggest that the two complexes interact with HS-DNA in the mode of intercalation with the intrinsic binding constants 5.0×10(4) M(-1) (1) and 6.7×10(4) M(-1) (2). The influence of structural variation of the terminal ligands in the tetranuclear complexes on DNA-binding properties is preliminarily discussed.
Tetranuclear complexes constructed from asymmetrical N,N′-bis(substituted)oxamide have been synthesized and characterized by X-ray single-crystal diffraction. The cytotoxicities and reactivities towards DNA of the two complexes have been investigated. [Display omitted] ► Two tetranuclear complexes have been synthesized and characterized. ► The two complexes exhibit cytotoxicities against SMMC-7721 and A549 cell lines. ► The DNA-binding abilities are consistent with cytotoxicities in the order 2>1. ► The terminal ligands are very important in the DNA-binding and cytotoxic properties. Two new circular tetranuclear copper(II) complexes, [Cu4(dmoxba)2(bpy)2(CH3OH)2](pic)2·2H2O (1) and [Cu4(dmoxba)2(phen)2](pic)2·2CH3OH (2), where dmoxba, pic, bpy and phen stand for the anion of 2-{N′-[2-(dimethylamino)ethyl]oxamido}benzoate, picrate, 2,2′-bipyridine and 1,10-phenanthroline, respectively, have been synthesized and structurally characterized by X-ray single-crystal diffraction. Both the complexes have embedded inversion centers and similar complex cations assembled by the oxamide-bridges and carboxylate-bridges of two cis-dmoxba3− ligands. The Cu⋯Cu separations through the oxamide-bridge and the carboxylato-bridge are 5.1991(4) and 5.4674(4)Å in 1 and 5.1843(5) and 5.2138(5)Å in 2, respectively. Both copper(II) ions are in square-pyramidal environments in 1. While in complex 2, the inner and exo copper(II) ions have square-planar and square-pyramidal coordination geometries, respectively. In both the crystals, three-dimensional supramolecular structures are formed by hydrogen bonds and π–π stacking interactions. The DNA-binding properties and anticancer activities of the two complexes were investigated. The results suggest that the two complexes interact with HS-DNA in the mode of intercalation with the intrinsic binding constants 5.0×104M−1 (1) and 6.7×104M−1 (2). The influence of structural variation of the terminal ligands in the tetranuclear complexes on DNA-binding properties is preliminarily discussed.
Two new circular tetranuclear copper(II) complexes, [Cu(4)(dmoxba)(2)(bpy)(2)(CH(3)OH)(2)](pic)(2)·2H(2)O (1) and [Cu(4)(dmoxba)(2)(phen)(2)](pic)(2)·2CH(3)OH (2), where dmoxba, pic, bpy and phen stand for the anion of 2-{N'-[2-(dimethylamino)ethyl]oxamido}benzoate, picrate, 2,2'-bipyridine and 1,10-phenanthroline, respectively, have been synthesized and structurally characterized by X-ray single-crystal diffraction. Both the complexes have embedded inversion centers and similar complex cations assembled by the oxamide-bridges and carboxylate-bridges of two cis-dmoxba(3-) ligands. The Cu···Cu separations through the oxamide-bridge and the carboxylato-bridge are 5.1991(4) and 5.4674(4) Å in 1 and 5.1843(5) and 5.2138(5) Å in 2, respectively. Both copper(II) ions are in square-pyramidal environments in 1. While in complex 2, the inner and exo copper(II) ions have square-planar and square-pyramidal coordination geometries, respectively. In both the crystals, three-dimensional supramolecular structures are formed by hydrogen bonds and π-π stacking interactions. The DNA-binding properties and anticancer activities of the two complexes were investigated. The results suggest that the two complexes interact with HS-DNA in the mode of intercalation with the intrinsic binding constants 5.0×10(4) M(-1) (1) and 6.7×10(4) M(-1) (2). The influence of structural variation of the terminal ligands in the tetranuclear complexes on DNA-binding properties is preliminarily discussed.Two new circular tetranuclear copper(II) complexes, [Cu(4)(dmoxba)(2)(bpy)(2)(CH(3)OH)(2)](pic)(2)·2H(2)O (1) and [Cu(4)(dmoxba)(2)(phen)(2)](pic)(2)·2CH(3)OH (2), where dmoxba, pic, bpy and phen stand for the anion of 2-{N'-[2-(dimethylamino)ethyl]oxamido}benzoate, picrate, 2,2'-bipyridine and 1,10-phenanthroline, respectively, have been synthesized and structurally characterized by X-ray single-crystal diffraction. Both the complexes have embedded inversion centers and similar complex cations assembled by the oxamide-bridges and carboxylate-bridges of two cis-dmoxba(3-) ligands. The Cu···Cu separations through the oxamide-bridge and the carboxylato-bridge are 5.1991(4) and 5.4674(4) Å in 1 and 5.1843(5) and 5.2138(5) Å in 2, respectively. Both copper(II) ions are in square-pyramidal environments in 1. While in complex 2, the inner and exo copper(II) ions have square-planar and square-pyramidal coordination geometries, respectively. In both the crystals, three-dimensional supramolecular structures are formed by hydrogen bonds and π-π stacking interactions. The DNA-binding properties and anticancer activities of the two complexes were investigated. The results suggest that the two complexes interact with HS-DNA in the mode of intercalation with the intrinsic binding constants 5.0×10(4) M(-1) (1) and 6.7×10(4) M(-1) (2). The influence of structural variation of the terminal ligands in the tetranuclear complexes on DNA-binding properties is preliminarily discussed.
Two new circular tetranuclear copper(II) complexes, [Cu4(dmoxba)2(bpy)2(CH3OH)2](pic)2ADT2H2O (1) and [Cu4(dmoxba)2(phen)2](pic)2ADT2CH3OH (2), where dmoxba, pic, bpy and phen stand for the anion of 2-{Na2-[2-(dimethylamino)ethyl]oxamido}benzoate, picrate, 2,2a2-bipyridine and 1,10-phenanthroline, respectively, have been synthesized and structurally characterized by X-ray single-crystal diffraction. Both the complexes have embedded inversion centers and similar complex cations assembled by the oxamide-bridges and carboxylate-bridges of two cis-dmoxba3a ligands. The Cua=Cu separations through the oxamide-bridge and the carboxylato-bridge are 5.1991(4) and 5.4674(4) Aa in 1 and 5.1843(5) and 5.2138(5) Aa in 2, respectively. Both copper(II) ions are in square-pyramidal environments in 1. While in complex 2, the inner and exo copper(II) ions have square-planar and square-pyramidal coordination geometries, respectively. In both the crystals, three-dimensional supramolecular structures are formed by hydrogen bonds and I-I stacking interactions. The DNA-binding properties and anticancer activities of the two complexes were investigated. The results suggest that the two complexes interact with HS-DNA in the mode of intercalation with the intrinsic binding constants 5.0 X 104 Ma1 (1) and 6.7 X 104 Ma1 (2). The influence of structural variation of the terminal ligands in the tetranuclear complexes on DNA-binding properties is preliminarily discussed.
Author Yan, Cui-Wei
Li, Yan-Tuan
Li, Xiao-Wen
Wu, Zhi-Yong
Zheng, Yong-Jun
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Keywords Carboxylate-bridge
Antitumor activity
Oxamidato-bridge
Tetracopper(II) complex
DNA-binding
Crystal structure
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Snippet Tetranuclear complexes constructed from asymmetrical N,N′-bis(substituted)oxamide have been synthesized and characterized by X-ray single-crystal diffraction....
Two new circular tetranuclear copper(II) complexes, [Cu₄(dmoxba)₂(bpy)₂(CH₃OH)₂](pic)₂·2H₂O (1) and [Cu₄(dmoxba)₂(phen)₂](pic)₂·2CH₃OH (2), where dmoxba, pic,...
Two new circular tetranuclear copper(II) complexes, [Cu(4)(dmoxba)(2)(bpy)(2)(CH(3)OH)(2)](pic)(2)·2H(2)O (1) and [Cu(4)(dmoxba)(2)(phen)(2)](pic)(2)·2CH(3)OH...
Two new circular tetranuclear copper(II) complexes, [Cu4(dmoxba)2(bpy)2(CH3OH)2](pic)2ADT2H2O (1) and [Cu4(dmoxba)2(phen)2](pic)2ADT2CH3OH (2), where dmoxba,...
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SubjectTerms Anions
antineoplastic agents
Antineoplastic Agents - chemical synthesis
Antineoplastic Agents - chemistry
Antineoplastic Agents - toxicity
Antitumor activity
Apoptosis - drug effects
Benzoates - chemistry
Carboxylate-bridge
cations
Cell Line, Tumor
Coordination Complexes - chemical synthesis
Coordination Complexes - chemistry
Coordination Complexes - toxicity
copper
Copper - chemistry
Crystal structure
Crystallography, X-Ray
crystals
DNA - metabolism
DNA-binding
Humans
Hydrogen Bonding
ligands
Molecular Conformation
Oxamidato-bridge
Phenanthrolines - chemistry
photobiology
photochemistry
Spectrophotometry, Ultraviolet
Tetracopper(II) complex
X-radiation
Title Synthesis and structure of new tetracopper(II) complexes bridged by 2-{N′-[2-(dimethylamino)ethyl]oxamido}benzoate: DNA-binding and anticancer activity
URI https://dx.doi.org/10.1016/j.jphotobiol.2012.05.004
https://www.ncbi.nlm.nih.gov/pubmed/22704662
https://www.proquest.com/docview/1027834129
https://www.proquest.com/docview/1038611447
https://www.proquest.com/docview/2000031821
Volume 114
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