首页> 外文期刊>Journal of Organometallic Chemistry >Synthesis, characterization and low temperature self assembling of (η~3-allyl)palladium complexes with 2-pyridyl-1,2,3-triazole bidentate ligands. Study of the catalytic activity in Suzuki-Miyaura reaction
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Synthesis, characterization and low temperature self assembling of (η~3-allyl)palladium complexes with 2-pyridyl-1,2,3-triazole bidentate ligands. Study of the catalytic activity in Suzuki-Miyaura reaction

机译:具有2-吡啶基-1,2,3-三唑二齿配体的(η〜3-烯丙基)钯配合物的合成,表征和低温自组装。铃木-宫浦反应的催化活性研究

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摘要

The cationic complexes [Pd(η 3-C 3H 5)(2-((4-propyl-1H-1,2,3-triazol-1-yl)methyl)pyridine)](X) (2: X = BF 4 -, 3: X = ClO 4 -), and [Pd(η 3-2-CH 3-C 3H 4)(2-((4-propyl- 1H-1,2,3-triazol-1-yl)methyl)-pyridine)](BF 4 -) (4) have been synthesized by reacting the appropriate palladium-allyl precursor with 2-((4-propyl-1H-1,2,3-triazol-1-yl)methyl)pyridine in the presence of AgBF 4 or AgClO 4. The solid-state structure of 2 has been determined by single-crystal X-ray diffraction analysis. According to 1H NMR spectroscopy the allyl protons undergo syn-syn, anti-anti exchange. 1H NMR spectroscopy reveals that in acetone at temperatures lower than 223 K these complexes form aggregates the stability of which is attributed to solvophobic interactions. Complex 2 is an active catalyst for the S-M coupling of aryl bromides with phenylboronic acid; good reaction rates are obtained only with activated substrates, whereas with deactivated substrates catalyst decomposition to palladium black occurs.
机译:阳离子络合物[Pd(η3-C 3H 5)(2-((4-丙基-1H-1,2,3-三唑-1-基)甲基)吡啶)](X)(2:X = BF 4-,3:X = ClO 4-)和[Pd(η3-2-CH 3-C 3H 4)(2-((4-丙基-1H-1,2,3-三唑-1-基)甲基)-吡啶)](BF 4-)(4)已通过使合适的钯-烯丙基前体与2-((4-丙基-1H-1,2,3-三唑-1-基)甲基AgBF 4或AgClO 4的存在下,吡啶基)的吡啶。2的固态结构已通过单晶X射线衍射分析确定。根据1H NMR光谱,烯丙基质子经历顺-反,抗-反交换。 1H NMR光谱表明,在丙酮中,温度低于223 K,这些配合物形成聚集体,其稳定性归因于疏溶剂相互作用。络合物2是芳基溴化物与苯基硼酸的S-M偶联的活性催化剂。仅在活化的底物上才能获得良好的反应速率,而在失活的底物上会发生催化剂分解为钯黑的现象。

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