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April 10, 2026Russian Journal of Inorganic Chemistry0 citations

Synthesis, Structural Features, and Antiproliferative Activity of Heteroligand Palladium(II) Complex Containing an Acyclic Diaminocarbene Ligand

MKM. V. KashinaMKM. A. Kinzhalov

Key Points

  • The research aims to synthesize and investigate the structure and biological activity of a palladium(II) heteroligand complex.
  • Synthesis of trans-[PdCl(CNXyl)2(C{CN(H)Xyl}2)]Cl complex
  • Structural analysis using X-ray diffraction and NMR spectroscopy
  • Investigation of antiproliferative activity against MDA-MB-231 cell line
  • Complex shows significant antiproliferative activity with an IC50 of 5.55 ± 0.45 µM
  • Activity is four times greater than that of cisplatin
  • Stabilization through N–H···Cl– hydrogen bonds confirmed by structural analysis

Abstract

This article presents the synthesis and detailed structural investigation of a new palladium (II) heteroligand complex trans-PdCl (CNXyl) 2 (CCN (H) Xyl2) Cl, containing an acyclic diaminocarbene ligand and two isocyanide ligands. X-ray diffraction and NMR spectroscopy revealed that complex is stabilized both in the crystal and in solution by a system of N–H···Cl– hydrogen bonds formed between one chloride anion and two N–H groups of the diaminocarbene ligand (N–H···Cl–···H–N), with calculated energies of 3. 8–5. 4 kcal/mol. A Cambridge Structural Database search identified 22 other palladium (II) acyclic diaminocarbene complexes with similar N–H···X···H–N (X = Cl–, Br–, O=C<, O=S<, etc. ) hydrogen-bonded systems. The complex demonstrated significant antiproliferative activity against the triple-negative breast cancer cell line MDA-MB-231, with an IC50 value of 5. 55 ± 0. 45 µM, which is four times higher than that of cisplatin.

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Cite This Study

Kashina et al. (2026) studied this question.

synapsesocial.com/papers/69d895486c1944d70ce063dchttps://doi.org/10.1134/s0036023625603356
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