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首页> 外文期刊>Journal of Organometallic Chemistry >Palladium selenolates via oxidative addition of organylselenenyl halides to palladium(0) precursor and via cleavage reaction of diselenides: Synthesis, structure and spectroscopic investigation
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Palladium selenolates via oxidative addition of organylselenenyl halides to palladium(0) precursor and via cleavage reaction of diselenides: Synthesis, structure and spectroscopic investigation

机译:通过将有机基硒基卤化物氧化加成到钯(0)前体以及通过二硒化物的裂解反应,硒化钯:合成,结构和光谱研究

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摘要

Oxidative addition of bis[2-(4,4-dimethyl-2-oxazolinyl)phenyl] diselenide to Pd(PPh3)4 provided two different mononuclear palladium selenolato complexes, Pd(Se∩N)(PPh3)Cl (4) [Se∩N = chelating 2-(4,4-dimethyl-2-oxazolinyl)phenylselenolate] and Pd(Se∩N)(Se∩N*) (PPh3) (5) [Se∩N = chelating, Se∩N* = non-chelating 2-(4,4-dimethyl-2-oxazolinyl)phenylselenolato ligand] in dicholoromethane and toluene respectively. Complex 4 has also been synthesized by the oxidative addition of 2-(4,4-dimethyl-2-oxazolinyl)phenylselenenyl chloride to Pd(PPh 3)4. The bromo and iodo analogs of 4 (9 and 10) were similarly synthesized by the oxidative addition of 2-(4,4-dimethyl-2-oxazolinyl) phenylselenenyl bromide and iodide, respectively to Pd(PPh3) 4. The oxidative addition of 2-(N,N-dimethylaminomethyl) phenylselenenyl bromide and iodide to Pd(PPh3)4 afforded mononuclear palladium selenolate complexes, Pd(Se∩N)(PPh3)X (13 and 14) [Se∩N = chelating 2-(N,N-dimethylaminomethyl)phenylselenolate, X = Br: 13, X = I: 14]. The reactions of bis[2-(4,4-dimethyl-2-oxazolinyl)phenyl] diselenide and bis[2-(N,N-dimethylaminomethyl)phenyl] diselenide with Pd(COD)Cl2 provided dinuclear selenolato-bridged complexes [PdCl(Se∩N)]2 (15) [Se∩N = chelating 2-(4,4-dimethyl-2- oxazolinyl)phenylselenolate] and [PdCl(Se∩N)]2 (19) [Se∩N = chelating 2-(N,N-dimethylaminomethyl)phenylselenolate] respectively. The complexes were characterized by elemental analysis and NMR (~1H and 77Se) spectroscopy. Complexes 4 and 5 were also characterized by mass spectrometry. Molecular structures of 4, 5, 9, 14 and 15 have been established by single crystal X-ray diffraction analysis. Complexes 4 and 9 are isomorphous and crystallize in the space group P2_1/c of the monoclinic system where the selenolato and halo ligands are trans to each other. Complex 5 crystallizes in the space group P21 of the monoclinic system where one chelating and one non-chelating selenolato ligands are trans to each other. Mononuclear complex 14 and binuclear centrosymmetric complex 15 crystallize in the P1 space group of the triclinic system.
机译:将双[2-(4,4-二甲基-2-恶唑啉基)苯基]二硒化物氧化添加到Pd(PPh3)4中可提供两种不同的单核硒硒化钯配合物Pd(Se∩N)(PPh3)Cl(4)[Se ∩N=螯合2-(4,4-二甲基-2-恶唑啉基)苯基硒酸酯]和Pd(Se∩N)(Se∩N*)(PPh3)(5)[Se∩N=螯合,Se∩N* =非螯合的2-(4,4-二甲基-2-恶唑啉基)苯基硒烯基配体]在二氯甲烷中和甲苯中。还通过将2-(4,4-二甲基-2-恶唑啉基)苯基硒烯基氯氧化加成到Pd(PPh 3)4中来合成配合物4。通过分别将2-(4,4-二甲基-2-恶唑啉基)苯基硒烯基溴化物和碘化物氧化添加到Pd(PPh3)4中,类似地合成4(9和10)的溴代和碘代类似物。 2-(N,N-二甲基氨基甲基)苯基硒基溴化物和碘化物与Pd(PPh3)4生成单核硒化​​钯钯络合物Pd(Se∩N)(PPh3)X(13和14)[Se∩N=螯合2-(N ,N-二甲基氨基甲基)苯基硒酸酯,X = Br:13,X = I:14]。双[2-(4,4-二甲基-2-恶唑啉基)苯基]二硒化物和双[2-(N,N-二甲基氨基甲基)苯基]二硒化物与Pd(COD)Cl2的反应提供了双核硒代桥联络合物[PdCl (Se∩N)] 2(15)[Se∩N=螯合2-(4,4-二甲基-2-恶唑啉基)苯基硒酸酯]和[PdCl(Se∩N)] 2(19)[Se∩N=螯合2-(N,N-二甲基氨基甲基)苯基硒酸酯]。通过元素分析和NMR(〜1H和77Se)光谱对复合物进行表征。配合物4和5也通过质谱表征。通过单晶X射线衍射分析已经确定了4、5、9、14和15的分子结构。配合物4和9是同晶的,并且在单斜晶系的空间群P2_1 / c中结晶,在该空间群中硒代和卤素配体彼此反型。配合物5在单斜晶系的空间群P21 / n中结晶,在该空间群中,一种螯合硒原子和一种非螯合硒原子配体彼此反式。单核复合物14和双核中心对称复合物15在三斜晶系的P1空间群中结晶。

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