Dhar, Shanta Nethaji, Munirathinam Chakravarty, Akhil R. Steric Protection of a Photosensitizer in a <i>N,N</i>-Bis[2-(2-pyridyl)ethyl]-2-phenylethylamine-copper(II) Bowl that Enhances Red Light-Induced DNA Cleavage Activity Ternary copper(II) complexes [Cu(py<sub>2</sub>phe)B](ClO<sub>4</sub>)<sub>2</sub> (<b>1</b>−<b>3</b>), where py<sub>2</sub>phe is a tripodal ligand <i>N</i>,<i>N</i>-bis[2-(2-pyridyl)ethyl]-2-phenylethylamine and B is a heterocyclic base (viz., 1,10-phenanthroline (phen, <b>1</b>), dipyrido[3,2-d:2‘,3‘-f]quinoxaline (dpq, <b>2</b>), or dipyrido[3,2-a:2‘,3‘-c]phenazine (dppz, <b>3</b>)), are prepared and their DNA-binding and photoinduced DNA-cleavage activities are studied. Complex <b>1</b> has been structurally characterized by single crystal X-ray crystallography. The molecular structure shows an axially elongated square-pyramidal (4 + 1) coordination geometry in which the phen ligand binds at the basal plane. The tripodal ligand py<sub>2</sub>phe displays an axial−equatorial binding mode with the amine nitrogen bonded at the axial site. A chemically significant CH−π interaction involving the CH moiety of the phenyl group of the tripodal ligand and the aromatic ring of phen is observed. The complexes display good binding propensity to calf thymus DNA giving a relative order of <b>3</b> (dppz) > <b>2</b> (dpq) > <b>1 </b>(phen). The DNA binding constants (<i>K</i><sub>b</sub>) for <b>1</b>−<b>3</b>, determined from absorption spectral studies, are 6.2 × 10<sup>3</sup>, 1.0 × 10<sup>4</sup>, and 5.7 × 10<sup>4</sup> M<sup>-1</sup>, respectively. The complexes show chemical nuclease activity in the presence of 3-mercaptopropionic acid as a reducing agent forming hydroxyl radicals as the cleavage active species. The photoinduced DNA-cleavage activity of the complexes has been studied using UV radiation of 365 nm and red light of 632.8 and 694 nm. The phen complex in absence of any photosensitizing moiety does not show any DNA cleavage upon photoirradiation. The dpq and dppz ligands with their photoactive quinoxaline and phenazine moieties display significant photoinduced DNA-cleavage activity. The dppz complex is more active than its dpq analogue because of the better steric protection of the DNA-bound photosensitizing dppz ligand from the solvent molecules. Control experiments reveal the formation of singlet oxygen in the light-induced DNA-cleavage reactions. The observed efficient photoinduced DNA-cleavage activity of <b>2</b> and <b>3</b> is akin to the “light switch” effect known for the tris-chelates of ruthenium(II). complexes show chemical nuclease activity;CH moiety;UV radiation;py 2 phe;Steric Protection;365 nm;694 nm;dpq analogue;hydroxyl radicals;heterocyclic base;phen ligand;tripodal ligand py 2 phe displays;amine nitrogen;Complex 1;complexes display;K b;DNA cleavage;calf thymus DNA;tripodal ligand N;singlet oxygen;phenazine moieties display;DNA binding constants;basal plane;control experiments;dppz ligands;tripodal ligand;photoactive quinoxaline;photoinduced;steric protection;phenyl group;binding propensity;photosensitizing moiety 2005-11-28
    https://acs.figshare.com/articles/journal_contribution/Steric_Protection_of_a_Photosensitizer_in_a_i_N_N_i_Bis_2_2_pyridyl_ethyl_2_phenylethylamine_copper_II_Bowl_that_Enhances_Red_Light_Induced_DNA_Cleavage_Activity/3254590
10.1021/ic0505246.s002