4.6 Article

Oxalato bridged coordination polymer of manganese(iii) involving unconventional OMIDLINE HORIZONTAL ELLIPSISπ-hole(nitrile) and antiparallel nitrileMIDLINE HORIZONTAL ELLIPSISnitrile contacts: antiproliferative evaluation and theoretical studies

Journal

NEW JOURNAL OF CHEMISTRY
Volume 44, Issue 46, Pages 20021-20038

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0nj03712e

Keywords

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Funding

  1. University Grants Commission (UGC), New Delhi [42-377/2013]
  2. ASTEC, DST, Govt. of Assam [ASTEC/S&T/206/2015-16/015]
  3. MICIU/AEI of Spain [CTQ2017-85821-R]

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A new oxalato bridged polymeric Mn(iii) coordination compound, {[Mn-2(eta(2)-C2O4)(H2O)(2)Cl-4] 2(4-CNpy)}(n) (1) (C2O4 = oxalate, 4-CNpy = 4-cyanopyridine), has been synthesized and characterized using elemental analysis, and spectroscopic (IR, electronic, XPS) and single crystal X-ray diffraction techniques. Electronic and XPS analyses of the compound justify the presence of a Mn(iii) center that is charge compensated by the two chlorido ligands and the oxygen atom of the bridged oxalate. 4-CNpy molecules in the lattice form unconventional H-bonded supramolecular dimers in the solid state assisted by antiparallel CNMIDLINE HORIZONTAL ELLIPSISCN dipoleMIDLINE HORIZONTAL ELLIPSISdipole interactions, which has been confirmed using QTAIM and NCI plot analysis and supported by MEP surface analysis. Remarkably, this dimer concurrently establishes a weak anion-pi interaction with the coordinated chlorido ligand. Unexpectedly, QTAIM analysis reveals the existence of an interesting OMIDLINE HORIZONTAL ELLIPSIS pi-hole(nitrile) contact involving the coordinated water molecule and the nitrile moiety that also contributes to the stabilization of the dimer in the crystal structure. To the best of our knowledge, the existence of such pi-hole interaction involving nitrile derivatives has not been reported before. Compound 1 has been further screened for anticancer activity in the malignant Dalton's lymphoma (DL) cell line and the results were confirmed by molecular docking and pharmacophore features. Our findings indicated that the cytotoxicity of compound 1 is initially increased in a dose dependent manner (0.01-1 mu M) and then decreased (5-10 mu M), which is also affected by the reactive oxygen species (ROS) in the cells. Interestingly, very low cytotoxicity (5-14%) was observed in the case of healthy cells (PBMC) for similar experimental conditions.

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