Photosensitizer in a molecular bowl and its effect on the DNA-binding and -cleavage activity of 3d-metal scorpionates

Sovan Roy, Ashis K. Patra, Shanta Dhar, Akhil R. Chakravarty

Research output: Contribution to journalArticle

42 Citations (Scopus)

Abstract

Ternary 3d-metal complexes [M(TpPh)(B)](ClO4) (1-8), where M is Co(II), Ni(II), Cu(II) and Zn(II), TpPh is anionic tris(3-phenylpyrazolyl)borate, and B is N,N-donor heterocyclic base, namely, 1,10-phenanthroline (phen, 1-4) and dipyrido[3,2-d:2′,3′-f] quinoxaline (dpq, 5-8), were prepared from a reaction of the perchlorate salt of the metal with KTpPh and B in CH2Cl2. The complexes were characterized by various physicochemical methods. 4-6 and 8 were structurally characterized by single-crystal X-ray crystallography. The crystal structures of the complexes show the presence of discrete cationic complexes having a square-pyramidal (4 + 1) coordination geometry in which two nitrogen atoms of the phenanthroline base (B) and two nitrogen atoms of the Tp Ph ligand occupy the basal plane and one nitrogen of the Tp Ph ligand binds at the axial site. The phenyl groups of the Tp Ph form a bowl-shaped structure that essentially encloses the {M(phen/dpq)} moiety. DNA-binding studies were carried out using various spectral techniques and from viscosity measurements. The complexes show moderate binding propensity to calf thymus DNA at the minor groove, giving binding constant values (Kb) of ∼104 M-1. The complexes exhibit poor DNA-cleavage activity in the dark in the presence of 3-mercaptopropionic acid (MPA) or hydrogen peroxide (H2O 2). The photoinduced DNA-cleavage activity of the complexes was investigated using UV-A radiation of 365 nm and visible light of two different wavelengths with a tunable multicolor Ar-Kr mixed gas ion laser source. The dpq complexes show efficient photoinduced DNA-cleavage activity via a metal-assisted photoexcitation process involving the formation of singlet oxygen as the cleavage active species in a type-II pathway. The paramagnetic d 7-Co(II)-dpq and d9-Cu(II)-dpq complexes exhibit efficient DNA-cleavage activity in visible light. The paramagnetic d8-Ni(II)- dpq complex displays only minor DNA-cleavage activity in visible light. Diamagnetic d10-Zn(II)-dpq complex shows only UV-A light-induced DNA cleavage but no apparent DNA-cleavage activity in visible light. Steric protection of the photoactive quinoxaline moiety of the dpq ligand inside the hydrophobic {M(TpPh)} molecular bowl has a positive effect on the photoinduced DNA-cleavage activity.

Original languageEnglish (US)
Pages (from-to)5625-5633
Number of pages9
JournalInorganic Chemistry
Volume47
Issue number13
DOIs
StatePublished - Jul 7 2008
Externally publishedYes

Fingerprint

Photosensitizing Agents
cleavage
deoxyribonucleic acid
Metals
DNA
metals
Quinoxalines
Nitrogen
quinoxalines
Ligands
nitrogen atoms
ligands
3-Mercaptopropionic Acid
Atoms
Singlet Oxygen
Borates
Phenanthrolines
Photoexcitation
X ray crystallography
Coordination Complexes

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Inorganic Chemistry

Cite this

Photosensitizer in a molecular bowl and its effect on the DNA-binding and -cleavage activity of 3d-metal scorpionates. / Roy, Sovan; Patra, Ashis K.; Dhar, Shanta; Chakravarty, Akhil R.

In: Inorganic Chemistry, Vol. 47, No. 13, 07.07.2008, p. 5625-5633.

Research output: Contribution to journalArticle

Roy, Sovan ; Patra, Ashis K. ; Dhar, Shanta ; Chakravarty, Akhil R. / Photosensitizer in a molecular bowl and its effect on the DNA-binding and -cleavage activity of 3d-metal scorpionates. In: Inorganic Chemistry. 2008 ; Vol. 47, No. 13. pp. 5625-5633.
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abstract = "Ternary 3d-metal complexes [M(TpPh)(B)](ClO4) (1-8), where M is Co(II), Ni(II), Cu(II) and Zn(II), TpPh is anionic tris(3-phenylpyrazolyl)borate, and B is N,N-donor heterocyclic base, namely, 1,10-phenanthroline (phen, 1-4) and dipyrido[3,2-d:2′,3′-f] quinoxaline (dpq, 5-8), were prepared from a reaction of the perchlorate salt of the metal with KTpPh and B in CH2Cl2. The complexes were characterized by various physicochemical methods. 4-6 and 8 were structurally characterized by single-crystal X-ray crystallography. The crystal structures of the complexes show the presence of discrete cationic complexes having a square-pyramidal (4 + 1) coordination geometry in which two nitrogen atoms of the phenanthroline base (B) and two nitrogen atoms of the Tp Ph ligand occupy the basal plane and one nitrogen of the Tp Ph ligand binds at the axial site. The phenyl groups of the Tp Ph form a bowl-shaped structure that essentially encloses the {M(phen/dpq)} moiety. DNA-binding studies were carried out using various spectral techniques and from viscosity measurements. The complexes show moderate binding propensity to calf thymus DNA at the minor groove, giving binding constant values (Kb) of ∼104 M-1. The complexes exhibit poor DNA-cleavage activity in the dark in the presence of 3-mercaptopropionic acid (MPA) or hydrogen peroxide (H2O 2). The photoinduced DNA-cleavage activity of the complexes was investigated using UV-A radiation of 365 nm and visible light of two different wavelengths with a tunable multicolor Ar-Kr mixed gas ion laser source. The dpq complexes show efficient photoinduced DNA-cleavage activity via a metal-assisted photoexcitation process involving the formation of singlet oxygen as the cleavage active species in a type-II pathway. The paramagnetic d 7-Co(II)-dpq and d9-Cu(II)-dpq complexes exhibit efficient DNA-cleavage activity in visible light. The paramagnetic d8-Ni(II)- dpq complex displays only minor DNA-cleavage activity in visible light. Diamagnetic d10-Zn(II)-dpq complex shows only UV-A light-induced DNA cleavage but no apparent DNA-cleavage activity in visible light. Steric protection of the photoactive quinoxaline moiety of the dpq ligand inside the hydrophobic {M(TpPh)} molecular bowl has a positive effect on the photoinduced DNA-cleavage activity.",
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N2 - Ternary 3d-metal complexes [M(TpPh)(B)](ClO4) (1-8), where M is Co(II), Ni(II), Cu(II) and Zn(II), TpPh is anionic tris(3-phenylpyrazolyl)borate, and B is N,N-donor heterocyclic base, namely, 1,10-phenanthroline (phen, 1-4) and dipyrido[3,2-d:2′,3′-f] quinoxaline (dpq, 5-8), were prepared from a reaction of the perchlorate salt of the metal with KTpPh and B in CH2Cl2. The complexes were characterized by various physicochemical methods. 4-6 and 8 were structurally characterized by single-crystal X-ray crystallography. The crystal structures of the complexes show the presence of discrete cationic complexes having a square-pyramidal (4 + 1) coordination geometry in which two nitrogen atoms of the phenanthroline base (B) and two nitrogen atoms of the Tp Ph ligand occupy the basal plane and one nitrogen of the Tp Ph ligand binds at the axial site. The phenyl groups of the Tp Ph form a bowl-shaped structure that essentially encloses the {M(phen/dpq)} moiety. DNA-binding studies were carried out using various spectral techniques and from viscosity measurements. The complexes show moderate binding propensity to calf thymus DNA at the minor groove, giving binding constant values (Kb) of ∼104 M-1. The complexes exhibit poor DNA-cleavage activity in the dark in the presence of 3-mercaptopropionic acid (MPA) or hydrogen peroxide (H2O 2). The photoinduced DNA-cleavage activity of the complexes was investigated using UV-A radiation of 365 nm and visible light of two different wavelengths with a tunable multicolor Ar-Kr mixed gas ion laser source. The dpq complexes show efficient photoinduced DNA-cleavage activity via a metal-assisted photoexcitation process involving the formation of singlet oxygen as the cleavage active species in a type-II pathway. The paramagnetic d 7-Co(II)-dpq and d9-Cu(II)-dpq complexes exhibit efficient DNA-cleavage activity in visible light. The paramagnetic d8-Ni(II)- dpq complex displays only minor DNA-cleavage activity in visible light. Diamagnetic d10-Zn(II)-dpq complex shows only UV-A light-induced DNA cleavage but no apparent DNA-cleavage activity in visible light. Steric protection of the photoactive quinoxaline moiety of the dpq ligand inside the hydrophobic {M(TpPh)} molecular bowl has a positive effect on the photoinduced DNA-cleavage activity.

AB - Ternary 3d-metal complexes [M(TpPh)(B)](ClO4) (1-8), where M is Co(II), Ni(II), Cu(II) and Zn(II), TpPh is anionic tris(3-phenylpyrazolyl)borate, and B is N,N-donor heterocyclic base, namely, 1,10-phenanthroline (phen, 1-4) and dipyrido[3,2-d:2′,3′-f] quinoxaline (dpq, 5-8), were prepared from a reaction of the perchlorate salt of the metal with KTpPh and B in CH2Cl2. The complexes were characterized by various physicochemical methods. 4-6 and 8 were structurally characterized by single-crystal X-ray crystallography. The crystal structures of the complexes show the presence of discrete cationic complexes having a square-pyramidal (4 + 1) coordination geometry in which two nitrogen atoms of the phenanthroline base (B) and two nitrogen atoms of the Tp Ph ligand occupy the basal plane and one nitrogen of the Tp Ph ligand binds at the axial site. The phenyl groups of the Tp Ph form a bowl-shaped structure that essentially encloses the {M(phen/dpq)} moiety. DNA-binding studies were carried out using various spectral techniques and from viscosity measurements. The complexes show moderate binding propensity to calf thymus DNA at the minor groove, giving binding constant values (Kb) of ∼104 M-1. The complexes exhibit poor DNA-cleavage activity in the dark in the presence of 3-mercaptopropionic acid (MPA) or hydrogen peroxide (H2O 2). The photoinduced DNA-cleavage activity of the complexes was investigated using UV-A radiation of 365 nm and visible light of two different wavelengths with a tunable multicolor Ar-Kr mixed gas ion laser source. The dpq complexes show efficient photoinduced DNA-cleavage activity via a metal-assisted photoexcitation process involving the formation of singlet oxygen as the cleavage active species in a type-II pathway. The paramagnetic d 7-Co(II)-dpq and d9-Cu(II)-dpq complexes exhibit efficient DNA-cleavage activity in visible light. The paramagnetic d8-Ni(II)- dpq complex displays only minor DNA-cleavage activity in visible light. Diamagnetic d10-Zn(II)-dpq complex shows only UV-A light-induced DNA cleavage but no apparent DNA-cleavage activity in visible light. Steric protection of the photoactive quinoxaline moiety of the dpq ligand inside the hydrophobic {M(TpPh)} molecular bowl has a positive effect on the photoinduced DNA-cleavage activity.

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