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Dinuclear Bridged Biphosphinic and Mononuclear Cyclopalladated Complexes of Benzylamines: Synthesis, Structural Characterization and Antitumor Activity Publisher



Karami K1 ; Kharat MH1 ; Sadeghialiabadi H2 ; Lipkowski J3 ; Mirian M2
Authors
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Authors Affiliations
  1. 1. Department of Chemistry, Isfahan University of Technology, Isfahan 84156/83111, Iran
  2. 2. Department of Pharmaceutical Chemistry, Faculty of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Institute of Physical Chemistry, Polish Academy of Sciences, 01-224 Warsaw, Kasprzaka 44/52, Poland

Source: Polyhedron Published:2013


Abstract

Reaction of chloro-bridged dinuclear palladacycles, [Pd2{(C,N)- C6H4CH2NH(R)}2(μ-Cl) 2] (R = Et (1a); R = t-Bu (1b)) with pyridine and PPh3 in the 1:2 M ratio at room temperature was used to prepare the mononuclear complexes, [Pd(C,N)-C6H4CH2NH(R)Cl(L)] (R = Et and L = Py (2a); R = t-Bu and L = PPh3 (2b)). Bridged biphosphinic palladacycle, [Pd2(C,N-dmba)2(μ-dppe)(Cl)2] (2c), (where dmba = N,N-dimethylbenzylamine and dppe = 1,2- bis(diphenylphosphino)ethane) has been also synthesized. The complexes were fully characterized by elemental analysis, IR and NMR spectroscopies. In addition, the solid structures of palladacycles 2a and 2c were studied by single-crystal X-ray crystallography. In vitro cytotoxicity assays of the cyclopalladated complexes, (2a-2c) and cisplatin were evaluated against the Hela (human cervix carcinoma), HT-29 (colon cancer cell line), K562 (leukemia cancer cell line) and MDA-MB-468 (human breast carcinoma). The complexes 2a-2c display IC50 values in a μM range better than that of the antitumor drug cisplatin. © 2012 Elsevier Ltd. All rights reserved.