4.3 Article

Organoruthenium(II) compounds with pyridyl benzoxazole/benzthiazole moiety: studies on DNA/protein binding and enzyme mimetic activities

Journal

JOURNAL OF COORDINATION CHEMISTRY
Volume 70, Issue 10, Pages 1645-1666

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/00958972.2017.1309649

Keywords

Ruthenium(II) compound; X-ray structure; DNA/BSA binding; enzyme kinetic studies

Funding

  1. Department of Science and Technology, Ministry of Science and Technology [140098]
  2. University Grants Commission [540/20/DRS-I/2016(SAP-I)]
  3. Grants-in-Aid for Scientific Research [15K05548] Funding Source: KAKEN

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We report herein synthesis and characterization of four new organoruthenium(II) complexes of the type [RuH(CO)(PPh3)(2)(L-1,L-2)]Cl (1, 3) and [Ru(CO)(Cl)(2)(AsPh3)(L-1,L-2)] (2, 4) derived from the reaction of [RuHCl(CO)(EPh3)(3)] (E = P or As) with 2-(pyridine-2yl)benzoxazole (L-1) and 2-(pyridine-2yl)benzthiazole (L-2). Single-crystal X-ray diffraction data of 2 proved octahedral geometry of the complexes with a 1:1 ratio between the metal and the coordinated ligands. The binding affinities of 1-4 toward calf-thymus DNA (CT-DNA) and BSA were thoroughly studied by various spectroscopic techniques. Furthermore, the coordination compounds exhibit catecholase-like activities in the aerial oxidation of 3,5-di-tert-butylcatechol to the corresponding o-quinone and phosphatase-like activities in the hydrolysis of 4-nitrophenyl phosphate to 4-nitrophenolate ion. The kinetic parameters have been determined using Michaelis-Menten approach. The highest k(cat) values suggested that coordination compounds exhibit higher rates of catalytic efficacy.

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