Pasa, Salih; Gürler, Nedim; Temel, Hamdi; Rafikova, Khadichakhan; Aydemir, Murat

Boron complexes BL1 and BL2 were prepared from O-donor ligands, 2,2′-(1E,1′E)-(ethane-1,2-diylbis(azan-1-yl-1-ylidene))bis(methane-1-yl-1-ylidene)diphenol (L1) and 2,2′-(propane-1,3-diylbis(azan-1-yl-1-ylidene))bis(methane-1-yl-1-ylidene)diphenol (L2). The complexes were fully characterized by 1H and 13C NMR, LC-MS/MS, TGA/DTA, UV-Vis, elemental analysis, SEM, and FTIR. The transfer hydrogenation of acetophenone derivatives was investigated by the boron complexes in the presence of isoPrOH, as the hydrogen source, under basic condition with NaOH. The results showed that the boron complexes were promising catalytic precursors for transfer hydrogenation of aromatic ketones in 0.1 M isoPrOH solution (up to 99%). Both steric and electronic factors of this class of molecules had a significant impact on the catalytic properties.

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Korkmaz, S. Aslan; Karadag, A.; Korkmaz, N.; Andaç, O.; Gürbüz, N.; Özdemir, I.; Topkaya, R.

Five cyanide complexes, [Ni(N-bishydeten)Pd(CN)(4)] (1), [Cu(N-bishydeten)Pd(-CN)(2)(CN)(2)](n) (2), [Cu(N-bishydeten)(2)][Pd(CN)(4)] (3), [Zn(N-bishydeten)Pd(CN)(4)] (4), and [Cd(N-bishydeten)(2)][Pd(CN)(4)] (5) (N-bishydeten = N,N-bis(2-hydroxyethyl)-ethylenediamine), have been synthesized and characterized using various techniques. Different structures were formed when the M:L ratio was varied in copper complexes. The single-crystal X-ray diffraction analysis reveals that 2, a 1-D cyanide-bridged complex with 2,2-CT-type zigzag chain, was obtained by using 1:1M:L ratio whereas 3 was formed as a complex salt in a molar ratio of 1:2. The thermal stabilities determined from DTG(max) values of the first decomposition stages change in the order 1>5>4>3>2. Although an EPR signal was not observed for 1, the g parameters obtained from the EPR spectra of 2 and 3 indicate that Cu-II ions are located in tetragonally distorted octahedral sites (D-4h), and the ground state of the unpaired electron is (B-2(1g)). The magnetic behavior indicates a very small antiferromagnetic interaction below 10K for 1-3. In 3, there is a temperature-independent paramagnetism () due to the orbital moments of the d electrons. 1-3 were tested as catalysts in Suzuki and Heck coupling reactions.

AtıfWoS16·OpenAlex15

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Karadag, A.; Korkmaz, S. Aslan; Andaç, O.; Yerli, Y.; Topcu, Y.

Four cyano complexes, [Ni(N-bishydeten)Ni(CN)(4)](n) (c1), [Cu(N-bishydeten)(2)][Ni(CN)(4)] (c2), [Zn-2(N-bishydeten)(2)Ni(CN)(4)](n) (c3), and [Cd(N-bishydeten)(2)][Ni(CN)(4)] (c4), have been synthesized and characterized by FT-IR, elemental, and thermal analyses. The structures of c2 and c4 were determined by single-crystal X-ray diffraction studies; both structures contain isolated cations and anions. The c2 consists of [Cu(N-bishydeten)(2)](2+) with octahedrally coordinated Cu-II and diamagnetic [Ni(CN)(4)](2-), but c4 consists of [Cd(N-bishydeten)(2)](2+), in which Cd-II is eight coordinate with two tetradentate N-bishydeten and diamagnetic [Ni(CN)(4)](2-). The value of the shape measure S (degrees) indicates that the coordination geometry around Cd-II lies along D-2d [dodecahedron; (dd)], C-2v [bicapped trigonal prism; (btp)], and D-4d [square antiprism; (sap)] but close to D-2d and D-4d. Variable temperature magnetic susceptibility measurements of c1 and c2 show the presence of little antiferromagnetic interaction below 20 K. Thermal analyses reveal that first neutral N-bishydeten and then cyano ligands were liberated from the complexes.

AtıfWoS19·OpenAlex16

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