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首页> 外文期刊>Journal of Organometallic Chemistry >Cationic olefin Pd(II) complexes bearing alpha-iminoketone N,O-ligands: synthesis, intramolecular and interionic characterization and reactivity with olefins and alkynes
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Cationic olefin Pd(II) complexes bearing alpha-iminoketone N,O-ligands: synthesis, intramolecular and interionic characterization and reactivity with olefins and alkynes

机译:带有α-亚氨基酮N,O-配体的阳离子烯烃Pd(II)配合物:合成,分子内和离子间的表征以及与烯烃和炔烃的反应性

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Complexes [Pd(eta(1), eta(2)-5-OMe-(CH12)-H-8)(N,O)]BF4 (N,O = 2,6-(i-Pr)(2)(C6H3)N=C(Ph)-C(Ph)=O, 1; 2,6-(i-Pr)(2)(C6H3)N=C(Me)C(Ph)=O, 2; 2-benzoylpyridine, 3) were synthesized by the reactions of [Pd(eta(1),eta(2)-5-OMe-C8H12)Cl]2 with the suitable N,O-ligand. They were tested as catalysts for olefin or alkyne polymerizations. During such reactions 1-3 quantitatively transformed into their eta(1),eta(2)-1-OMe-C8H12 isomers (1a-3a). The same isomerization occurred in methylene chloride, even in the absence of olefins or alkynes, with a much slower rate. All complexes were fully characterized in solution by multinuclear and multidimensional low temperature NMR spectroscopy. The solid state structures of complexes 1 and la were investigated by X-ray single crystal studies. F-19,H-1-HOESY NMR experiments carried out in methylene chloride-d(2) at 217 K indicated that the anion prefers to locate on the side of N,O-ligand shifted toward the O-arm in 1-1a and 2-2a while it approaches the N-arm in 3 and 3a compounds. (C) 2003 Elsevier B.V. All rights reserved. [References: 55]
机译:配合物[Pd(eta(1),eta(2)-5-OMe-(CH12)-H-8)(N,O)] BF4(N,O = 2,6-(i-Pr)(2) (C6H3)N = C(Ph)-C(Ph)= O,1; 2,6-(i-Pr)(2)(C6H3)N = C(Me)C(Ph)= O,2; 2通过[Pd(eta(1),eta(2)-5-OMe-C8H12)Cl] 2与合适的N,O-配体反应合成-苯甲酰基吡啶3)。他们被测试为烯烃或炔烃聚合的催化剂。在此类反应过程中,1-3定量地转化为它们的eta(1),eta(2)-1-OMe-C8H12异构体(1a-3a)。即使在不存在烯烃或炔烃的情况下,在二氯甲烷中也发生了相同的异构化,其速率要慢得多。通过多核和多维低温NMR光谱在溶液中充分表征了所有络合物。通过X射线单晶研究研究了配合物1和1a的固态结构。在217 K的二氯甲烷-d(2)中进行的F-19,H-1-HOESY NMR实验表明,该阴离子更喜欢位于N,O-配体侧向1-1a中的O-臂侧移2-2a接近3和3a化合物中的N臂。 (C)2003 Elsevier B.V.保留所有权利。 [参考:55]

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