PEPPSI type complexes: Synthesis, x-ray structures, spectral studies, molecular docking and theoretical investigations


SERDAROĞLU G., ŞAHİN N., Ustun E., Tahir M. N., Arici C., GÜRBÜZ N., ...Daha Fazla

POLYHEDRON, cilt.204, 2021 (SCI-Expanded) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 204
  • Basım Tarihi: 2021
  • Doi Numarası: 10.1016/j.poly.2021.115281
  • Dergi Adı: POLYHEDRON
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Chemical Abstracts Core
  • Anahtar Kelimeler: N-heterocyclic carbenes, PEPPSI, Aromatic substituent effect, Quantum chemical calculations, Molecular docking, CARBENE-PALLADIUM COMPLEXES, N-HETEROCYCLIC CARBENES, AB-INITIO, ELECTRONIC-PROPERTIES, SILVER(I) COMPLEXES, FT-IR, ANGIOGENESIS, SUZUKI, ELECTROPHILICITY, PRECATALYST
  • İnönü Üniversitesi Adresli: Evet

Özet

In this work, three novel potent benzimidazolium-derived PEPPSI type palladium complexes, namely dichloro[1-allyl-3-benzylbenzimidazole-2-ylidene]pyridine palladium(II) (1), dichloro[1-allyl-3-(1-naphthylmethyl)benzimidazole-2-ylidene]pyridine palladium(II) (2) and dichloro[1-allyl-3-(9-anthrylmethyl)benzimidazole-2-ylidene]pyridine palladium(II) (3), were synthesized and characterized by single X-ray crystallography, FT-IR and NMR spectroscopy. The results were compared with the relevant calculated data. After structural and spectroscopic determination, the performance of the global reactivity behavior of these derivatives was evaluated by quantum chemical parameters (QCP) obtained from DFT/B3LYP and HF methods utilized with the 6-311 g**/LANL2DZ basis set. Next, NBO analyses were conducted to enlighten the possible interactions that occur for each derivative and this revealed that the main role in the lowering of the stabilization energies of all the derivatives was sourced from n -> pi* and pi -> pi* interactions. Finally, all the complexes were analyzed for their anticancer potential by the molecular docking method with VEGFR (vascular endothelial growth factor receptor), thioredoxin reductase, breast cancer and the dodecamer structure of DNA. (C) 2021 Elsevier Ltd. All rights reserved.