“…In the 1 H NMR spectra of ligands ( S ) ‐L 1 H and ( S ) ‐L 2 H , a singlet for the phenolic (OH) proton appeared at δ , 13.88 and 10.85 ppm, respectively. This OH proton was highly deshielded in ( S ) ‐L 1 H owing to the presence of strong OH⋯N intramolecular hydrogen bonding as observed generally in the Schiff bases of 2‐hydroxy aldehydes or ketones 39 . The peak for phenolic proton disappeared from the spectra of their respective complexes ( S ) ‐1 and ( S ) ‐2 , which confirmed the coordination of deprotonated ligands [( S ) ‐L 1 and ( S ) ‐L 2 ] through the phenolate (PhO − ) ion to the central Pd (II) ion.…”
A novel selenated Schiff base (S)‐L1H has been synthesized from (2S)‐1‐(benzylselanyl)‐3‐phenylpropan‐2‐amine which upon reduction formed a reduced Schiff base (S)‐L2H. Palladium (II) complexes (S)‐1 and (S)‐2 of ligands (S)‐L1H and (S)‐L2H respectively were successfully synthesized. The structures of all four compounds were thoroughly identified by analytical and various spectroscopic techniques. The absolute molecular structures of the above two complexes were further confirmed by single crystal X‐ray diffraction. Both (S)‐L1H and (S)‐L2H coordinated as monobasic ((S)‐L1–2), chelating, tridentate (Se,N,O−) ligands resulting in the complexes of composition (S)‐[PdCl(L1/2)] [(S)‐1/2]. In the crystals of complexes (S)‐1 and (S)‐2, there were moderate to strong Se⋯O, CH⋯Cl and CH⋯O types of intermolecular secondary interactions. CT‐DNA binding activity of these selenium‐containing ligands and their palladium complexes bearing a Pd–Se bond have been evaluated for the first time by performing electronic absorption titration and fluorescence emission quenching using CT‐DNA‐EB and viscometric experiments. These ligands and complexes exhibited remarkable DNA binding activity as shown by their intrinsic DNA binding constants (Kb) and Stern–Volmer constants (Ksv) in the ranges 5.2–9.9 × 104 and 3.6–4.7 × 104, respectively. The viscosity of CT‐DNA decreases with increasing concentration of these compounds. The results of the DNA‐binding studies revealed that all of the compounds interact with DNA at a minor groove which was further confirmed by molecular docking studies.
“…In the 1 H NMR spectra of ligands ( S ) ‐L 1 H and ( S ) ‐L 2 H , a singlet for the phenolic (OH) proton appeared at δ , 13.88 and 10.85 ppm, respectively. This OH proton was highly deshielded in ( S ) ‐L 1 H owing to the presence of strong OH⋯N intramolecular hydrogen bonding as observed generally in the Schiff bases of 2‐hydroxy aldehydes or ketones 39 . The peak for phenolic proton disappeared from the spectra of their respective complexes ( S ) ‐1 and ( S ) ‐2 , which confirmed the coordination of deprotonated ligands [( S ) ‐L 1 and ( S ) ‐L 2 ] through the phenolate (PhO − ) ion to the central Pd (II) ion.…”
A novel selenated Schiff base (S)‐L1H has been synthesized from (2S)‐1‐(benzylselanyl)‐3‐phenylpropan‐2‐amine which upon reduction formed a reduced Schiff base (S)‐L2H. Palladium (II) complexes (S)‐1 and (S)‐2 of ligands (S)‐L1H and (S)‐L2H respectively were successfully synthesized. The structures of all four compounds were thoroughly identified by analytical and various spectroscopic techniques. The absolute molecular structures of the above two complexes were further confirmed by single crystal X‐ray diffraction. Both (S)‐L1H and (S)‐L2H coordinated as monobasic ((S)‐L1–2), chelating, tridentate (Se,N,O−) ligands resulting in the complexes of composition (S)‐[PdCl(L1/2)] [(S)‐1/2]. In the crystals of complexes (S)‐1 and (S)‐2, there were moderate to strong Se⋯O, CH⋯Cl and CH⋯O types of intermolecular secondary interactions. CT‐DNA binding activity of these selenium‐containing ligands and their palladium complexes bearing a Pd–Se bond have been evaluated for the first time by performing electronic absorption titration and fluorescence emission quenching using CT‐DNA‐EB and viscometric experiments. These ligands and complexes exhibited remarkable DNA binding activity as shown by their intrinsic DNA binding constants (Kb) and Stern–Volmer constants (Ksv) in the ranges 5.2–9.9 × 104 and 3.6–4.7 × 104, respectively. The viscosity of CT‐DNA decreases with increasing concentration of these compounds. The results of the DNA‐binding studies revealed that all of the compounds interact with DNA at a minor groove which was further confirmed by molecular docking studies.
“…Various primary amines were produced with up to >99% ee and excellent yields upon using both aromatic and aliphatic sulfinylimines with 2-PrOH as the hydrogen source (Scheme ) . A new half-sandwich ruthenium compound readily prepared from [RuCl 2 ( p -cymene)] 2 with the Schiff base scaffold 78 was examined as catalyst in the TH of ketones, and up to 1260 h –1 TOF was obtained . Following the development of thio- ligand in ruthenium-catalyzed TH, a new cationic half-sandwich complex of the type [(η 6 -cymene)Ru(PPh 3 )(L)] + was synthesized as an air-stable salt.…”
Section: Recent Advances and Trends
In Th Using Transition-metal
Cata...mentioning
confidence: 99%
“…356 A new half-sandwich ruthenium compound readily prepared from [RuCl 2 (p-cymene)] 2 with the Schiff base scaffold 78 was examined as catalyst in the TH of ketones, and up to 1260 h −1 TOF was obtained. 357 Following the development of thio-ligand in rutheniumcatalyzed TH, 358 a new cationic half-sandwich complex of the type [(η 6 -cymene)Ru(PPh 3 )(L)] + was synthesized as an air-stable salt. This complex contains a thioamide ligand 79 that is coordinated to Ru as a bidentate O, S donor with a typical piano-stool geometry.…”
“…Selected IR data (KBr, cm −1 ); 3425(s),3056(w), 2931(w), 2847(w), 1607(s), 1535(m), 1463(s), 1385(m), 1311(w), 1221(w), 1186(w), 858(w), 742(m). λmax (nm) (ɛ(M − 1 cm −1 )): 245 (73,723), 313 (7204), 349 (4359) and 429 (17,146)…”
Section: Hydrav-ermentioning
confidence: 99%
“…Lanthanide(III) ions are the best ions with the largest size that are able to form stable complexes with high coordination numbers [11]. In between, lanthanide (III) complexes containing Schiff base provide a highly organized class of compounds with interesting properties such as antifungal [12], antibacterial [13], anticancer [14], catalytic [15], electroluminescence and fluorescence, sensing [16][17][18] biological activities [19], and unique magnetic properties [20].…”
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