SDS of cas: 91-02-1. Authors Pischedda, S; Stoccoro, S; Zucca, A; Sciortino, G; Ortu, F; Clarkson, GJ in ROYAL SOC CHEMISTRY published article about in [Pischedda, Sara; Stoccoro, Sergio; Zucca, Antonio] Univ Sassari, Dipartimento Chim & Farm, Via Vienna 2, I-07100 Sassari, Italy; [Pischedda, Sara; Stoccoro, Sergio; Zucca, Antonio] Consorzio Interuniv Reatt Chim & Catalisi CIRCC, Bari, Italy; [Sciortino, Giuseppe] Inst Chem Res Catalonia ICIQ, Av Paisos Catalans 16, Tarragona 43007, Spain; [Ortu, Fabrizio] Univ Leicester, Sch Chem, Univ Rd, Leicester LE1 7RH, Leics, England; [Ortu, Fabrizio] Univ Manchester, Dept Chem, Oxford Rd, Manchester M13 9PL, Lancs, England; [Clarkson, Guy J.] Univ Warwick, Dept Chem, Gibbet Hill Rd, Coventry CV4 7AL, W Midlands, England in 2021.0, Cited 77.0. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1
Several palladium(ii) and platinum(ii) complexes (1-20) of general formula [M(L-n)(X)(Y)] [M = Pd, X = Y = Cl (1-Cl-4-Cl), X = Y = OAc (1-OAc-4-OAc); M = Pt: X = Y = Cl (5-8); M = Pd, X = Cl, Y = CH3 (9-12); M = Pt, X = Cl, Y = CH3 (13-16) or X = Y = CH3 (17-20); n = 1-4] have been synthesized by reaction of different Pd(ii) and Pt(ii) derivatives with various 3-substituted 1-(2-pyridyl)-imidazo[1,5-a]pyridines; i.e.L-n = 1-(2-pyridyl)-3-arylimidazo[1,5-a]pyridine (aryl = Phenyl, L-1; 2-o-Tolyl, L-2; Mesityl, L-3) and 1-(2-pyridyl)-3-benzylimidazo[1,5-a]pyridine (L-4). Detailed spectroscopic investigation (including IR, mono- and bi-dimensional H-1 NMR) and elemental analysis has been performed for all these species, allowing their complete characterization. L-n act as N,N-bidentate ligands and coordinate the metal centers in a chelate fashion through the pyridyl (N-py) and the pyridine-like nitrogen atom of the imidazo[1,5-a]pyridine group (N-im). The X-ray structural analysis performed on two of Pd(ii) and three Pt(ii) complexes, namely [Pd(L-2)(CH3)Cl] (10), [Pd(L-3)(CH3)Cl] (11) and [Pt(L-1)Cl-2] (5), [Pt(L-4)Cl-2] (8), [Pt(L-2)(CH3)Cl] (14) confirmed the spectroscopic and analytical data. Finally DFT studies unveiled the structural reasons behind the inertia of the synthesised compounds toward metalation, identified as the higher angle steric strain in comparison with the analogous bipyridine complexes.
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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem