Palladium(II) complexes incorporating phenylazo arylmethine ancillary ligands: Synthesis, spectral and antitumor activity

A series of azoimine palladium(II) complexes of the general type cis-[PdCl2L] (1–6) {L = PhNNC(COMe)NC6H4X, where X = H (L1), CH3 (L2), Cl (L3), Br (L4), naphthyl (L5) and OMe (L6)} have been prepared by the reaction of cis-[PdCl2(NCPh)2] and the ligands (L) in acetone at room temperature. These c...

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Main Authors: Mousa Al-Noaimi, Adnan S. Abu-Surrah, Lubna Tahtamouni
Format: Article
Language:English
Published: Elsevier 2016-11-01
Series:Arabian Journal of Chemistry
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S187853521200055X
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spelling doaj-b0a1e525310a4982a3a786c1d29fac432020-11-24T21:27:17ZengElsevierArabian Journal of Chemistry1878-53522016-11-019S2S1503S150910.1016/j.arabjc.2012.03.009Palladium(II) complexes incorporating phenylazo arylmethine ancillary ligands: Synthesis, spectral and antitumor activityMousa Al-Noaimi0Adnan S. Abu-Surrah1Lubna Tahtamouni2Department of Chemistry, Hashemite University, P.O. Box 150459, Zarqa 13115, JordanDepartment of Chemistry, Hashemite University, P.O. Box 150459, Zarqa 13115, JordanDepartment of Biology and Biotechnology, Hashemite University, Zarqa, JordanA series of azoimine palladium(II) complexes of the general type cis-[PdCl2L] (1–6) {L = PhNNC(COMe)NC6H4X, where X = H (L1), CH3 (L2), Cl (L3), Br (L4), naphthyl (L5) and OMe (L6)} have been prepared by the reaction of cis-[PdCl2(NCPh)2] and the ligands (L) in acetone at room temperature. These complexes have been characterized by spectroscopic (IR-, UV–Vis and NMR) and electrochemical techniques. In addition, their biological activity has been studied via MTT test and by detecting the inhibition of clonal growth in three tumor cell lines, namely T47D human ductal breast carcinoma, MTLn3 murine mammary adenocarcinoma and RAW 264.7 murine leukemic monocyte macrophage. All of the tested palladium(II) complexes showed a noticeable antitumor activity. Complexes 4 and 5 showed a higher cytotoxic activity against human T47D breast tumor cell line than cisplatin, while comparable activity was observed against murine mammary MTLn3 adenocarcinoma cell line.http://www.sciencedirect.com/science/article/pii/S187853521200055XPalladium(II) complexesAzoimine ligandsT47D breast carcinomaMurine mammary MTLn3 adenocarcinomaRAW 264.7 leukemia cell line
collection DOAJ
language English
format Article
sources DOAJ
author Mousa Al-Noaimi
Adnan S. Abu-Surrah
Lubna Tahtamouni
spellingShingle Mousa Al-Noaimi
Adnan S. Abu-Surrah
Lubna Tahtamouni
Palladium(II) complexes incorporating phenylazo arylmethine ancillary ligands: Synthesis, spectral and antitumor activity
Arabian Journal of Chemistry
Palladium(II) complexes
Azoimine ligands
T47D breast carcinoma
Murine mammary MTLn3 adenocarcinoma
RAW 264.7 leukemia cell line
author_facet Mousa Al-Noaimi
Adnan S. Abu-Surrah
Lubna Tahtamouni
author_sort Mousa Al-Noaimi
title Palladium(II) complexes incorporating phenylazo arylmethine ancillary ligands: Synthesis, spectral and antitumor activity
title_short Palladium(II) complexes incorporating phenylazo arylmethine ancillary ligands: Synthesis, spectral and antitumor activity
title_full Palladium(II) complexes incorporating phenylazo arylmethine ancillary ligands: Synthesis, spectral and antitumor activity
title_fullStr Palladium(II) complexes incorporating phenylazo arylmethine ancillary ligands: Synthesis, spectral and antitumor activity
title_full_unstemmed Palladium(II) complexes incorporating phenylazo arylmethine ancillary ligands: Synthesis, spectral and antitumor activity
title_sort palladium(ii) complexes incorporating phenylazo arylmethine ancillary ligands: synthesis, spectral and antitumor activity
publisher Elsevier
series Arabian Journal of Chemistry
issn 1878-5352
publishDate 2016-11-01
description A series of azoimine palladium(II) complexes of the general type cis-[PdCl2L] (1–6) {L = PhNNC(COMe)NC6H4X, where X = H (L1), CH3 (L2), Cl (L3), Br (L4), naphthyl (L5) and OMe (L6)} have been prepared by the reaction of cis-[PdCl2(NCPh)2] and the ligands (L) in acetone at room temperature. These complexes have been characterized by spectroscopic (IR-, UV–Vis and NMR) and electrochemical techniques. In addition, their biological activity has been studied via MTT test and by detecting the inhibition of clonal growth in three tumor cell lines, namely T47D human ductal breast carcinoma, MTLn3 murine mammary adenocarcinoma and RAW 264.7 murine leukemic monocyte macrophage. All of the tested palladium(II) complexes showed a noticeable antitumor activity. Complexes 4 and 5 showed a higher cytotoxic activity against human T47D breast tumor cell line than cisplatin, while comparable activity was observed against murine mammary MTLn3 adenocarcinoma cell line.
topic Palladium(II) complexes
Azoimine ligands
T47D breast carcinoma
Murine mammary MTLn3 adenocarcinoma
RAW 264.7 leukemia cell line
url http://www.sciencedirect.com/science/article/pii/S187853521200055X
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AT adnansabusurrah palladiumiicomplexesincorporatingphenylazoarylmethineancillaryligandssynthesisspectralandantitumoractivity
AT lubnatahtamouni palladiumiicomplexesincorporatingphenylazoarylmethineancillaryligandssynthesisspectralandantitumoractivity
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