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For: Kargar H, Fallah-mehrjardi M, Behjatmanesh-ardakani R, Bahadori M, Moghadam M, Ashfaq M, Munawar KS, Tahir MN. Pd(II) and Ni(II) complexes containing ONNO tetradentate Schiff base ligand: Synthesis, crystal structure, spectral characterization, theoretical studies, and use of PdL as an efficient homogeneous catalyst for Suzuki–Miyaura cross-coupling reaction. Polyhedron 2022;213:115622. [DOI: 10.1016/j.poly.2021.115622] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Kargar H, Ashfaq M, Fallah-mehrjardi M, Behjatmanesh-ardakani R, Munawar KS, Tahir MN. Unsymmetrical Ni(II) Schiff base complex: Synthesis, spectral characterization, crystal structure analysis, Hirshfeld surface investigation, theoretical studies, and antibacterial activity. Journal of Molecular Structure 2022;1265:133381. [DOI: 10.1016/j.molstruc.2022.133381] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
2 Kargar H, Ashfaq M, Fallah-mehrjardi M, Behjatmanesh-ardakani R, Munawar KS, Tahir MN. Theoretical studies, Hirshfeld surface analysis, and crystal structure determination of a newly synthesized benzothiazole copper(II) complex. Journal of Molecular Structure 2022;1261:132905. [DOI: 10.1016/j.molstruc.2022.132905] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
3 Balakrishnan N, Haribabu J, Eshaghi Malekshah R, Swaminathan S, Balachandran C, Bhuvanesh N, Aoki S, Karvembu R. Effect of N-benzyl group in indole scaffold of thiosemicarbazones on the biological activity of their Pd(II) complexes: DFT, biomolecular interactions, in silico docking, ADME and cytotoxicity studies. Inorganica Chimica Acta 2022;534:120805. [DOI: 10.1016/j.ica.2022.120805] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
4 Gorjian H, Khaligh NG. 4,4′-Trimethylenedipiperidine, a safe and greener alternative for piperidine, catalyzed the synthesis of N-methyl imines. Res Chem Intermed. [DOI: 10.1007/s11164-022-04680-2] [Reference Citation Analysis]