The binding interaction of surfactant cobalt(III) complex, cis-[Co(bpy)(HA)](ClO), in which bpy is 2,2-bipyridine and HA is hexadecylamine or cetylamnine with DNA was through intercalative mode via the long aliphatic chains present in the ligands. The binding was investigated by various techniques, electronic absorption, fluorescence spectroscopy, circular dichroism (CD), cyclic voltametry (CV) and viscosimetry measurements. The spectroscopic studies together with cyclic voltammetry and viscosity experiments support that the surfactant cobalt(III) complex binds to calf thymus DNA by intercalation through the aliphatic chain present in the complex into the base pairs of DNA. The presence of bipyridine ligand with larger π-frame work may also enhance intercalation. UV-vis., spectrum showed 4 nm bathochromic shift of the absorption band at 352 nm along with significant hypochromicity for the absorption band of the complex. The intrinsic binding constants(at below and above CMC are K = 2.41 × 10M, K = 3.12 × 10M respectively) is more in keeping with intercalators and suggests this binding mode. The viscosity measurements showed that the surfactant cobalt(III) complex-DNA interaction can be hydrophobic and confirm intercalation. Moreover, the complex induced detectable changes in the CD spectrum of CT-DNA. Competitive binding study with ethidium bromide (EB) shows that the surfactant complex exhibits the ability to displace the DNA-bound EB indicating that the complex binds to DNA in strong competition with EB for the intercalative binding site. Also, CV results confirm this mode because, with increasing the CT-DNA concentration, shift to higher potential was observed. Besides the effect of binding of surfactant cobalt(III) complex to DNA in presence of β-cyclodextrin has also studied. This binding of the surfactant cobalt(III) complex in presence of β-cyclodextrin medium has been prevented (at below and above CMC are K = 5.45 × 10M, K = 6.92 × 10M respectively) due to the incorporation of the aliphatic chains into the cavity of β-cyclodextrin. In presence of β-cyclodextrin the binding occur through surface and (or) groove binding can be attributed to the inclusion of the long aliphatic chain that is present in one of the ligands into cyclodextrin.
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http://dx.doi.org/10.1016/j.saa.2022.122015 | DOI Listing |
Spectrochim Acta A Mol Biomol Spectrosc
February 2023
Battery Research Center for Green Energy, Ming Chi University of Technology, New Taipei City 24301, Taiwan.
The binding interaction of surfactant cobalt(III) complex, cis-[Co(bpy)(HA)](ClO), in which bpy is 2,2-bipyridine and HA is hexadecylamine or cetylamnine with DNA was through intercalative mode via the long aliphatic chains present in the ligands. The binding was investigated by various techniques, electronic absorption, fluorescence spectroscopy, circular dichroism (CD), cyclic voltametry (CV) and viscosimetry measurements. The spectroscopic studies together with cyclic voltammetry and viscosity experiments support that the surfactant cobalt(III) complex binds to calf thymus DNA by intercalation through the aliphatic chain present in the complex into the base pairs of DNA.
View Article and Find Full Text PDFJ Environ Sci Health A Tox Hazard Subst Environ Eng
May 2016
b Institute of Chemistry , Faculty of Natural Sciences and Mathematics , Ss. Cyril and Methodius University, Skopje , Republic of Macedonia.
Two new methods for the determination of iron by atomic absorption spectrometry (AAS) are proposed for drinking water. The determination was made after flotation concentration of Fe by using of two new flotation collectors: lead(II) heptyldithiocarbamate, Pb(HpDTC)2 and cobalt(III) heptyldithiocarbamate Co(HpDTC)3. All important parameters for the two proposed procedures were optimised (pH, mass of Pb, mass of Co, amount of HpDTC(-), type of surfactant, induction time, etc.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
August 2015
School of Chemistry, Bharathidasan University, Trichirappalli 620024, Tamilnadu, India. Electronic address:
The interaction of two surfactant cobalt(III) complexes, cis-[Co(ip)₂(DA)₂](ClO₄)₃ 1 and cis-[Co(dpq)₂(DA)₂](ClO₄)₃ 2 where ip=imidazo[4,5-f][1,10]phenanthroline and dpq=dipyrido[3,2-d:2'-3'-f]quinoxaline with yeast tRNA have been explored by using electronic absorption, competitive binding, electrochemical studies and viscosity measurements. The results suggest that these complexes can bind to tRNA by intercalation. The presence of hydrophobic diimine ligand and the long aliphatic double chains of these complexes facilitate its intercalative interaction with the hydrophobic interior of the tRNA.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
May 2015
School of Chemistry, Bharathidasan University, Tiruchirapalli 620024, Tamil Nadu, India.
The kinetics of outer sphere electron transfer reaction of surfactant cobalt(III) complex ions, cis-[Co(en)2(C12H25NH2)2](3+) (1), cis-[Co(dp)2(C12H25NH2)2](3+) (2), cis-[Co(trien)(C12H25NH2)2](3+) (3), cis-[Co(bpy)2(C12H25NH2)2](3+) (4) and cis-[Co(phen)2(C12H25NH2)2](3+) (5) (en: ethylenediamine, dp: diaminopropane, trien : triethylenetetramine, bpy: 2,2'-bipyridyl, phen: 1,10-phenanthroline and C12H25NH2 : dodecylamine) have been interrogated by Fe(2+) ion in ionic liquid (1-butyl-3-methylimidazoliumbromide) medium at different temperatures (298, 303, 308, 313, 318 and 323K) by the spectrophotometry method under pseudo first order conditions using an excess of the reductant. Experimentally the reactions were found to be of second order and the electron transfer as outer sphere. The second order rate constant for the electron transfer reaction in ionic liquids was found to increase with increase in the concentration of all these surfactant cobalt(III) complexes.
View Article and Find Full Text PDFJ Fluoresc
November 2014
School of Chemistry, Bharathidasan University, Tiruchirapalli, 620024, Tamilnadu, India,
A new surfactant cobalt(III) complex, cis-[Co(dpqc)2(DA)2](ClO4)3, where dpqc = dipyrido[3,2-a:2',4'-c](6,7,8,9-tetrahydro)phenazine and DA = dodecylamine, has been synthesized and characterized by elemental analysis, UV-Visible, IR and NMR spectra. The critical micelle concentration (CMC) value of this surfactant cobalt(III) complex in aqueous solution was obtained from conductance measurements. The conductivity data (at 303, 308, 313, 318 and 323 K) were used for the evaluation of the temperature-dependent CMC and the thermodynamics of micellization (ΔG(0) m, ΔH(0) m and ΔS(0) m).
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