首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Synthesis, characterization, X-ray crystallography analysis, and catalytic activity of bis(2-pyridylmethyl)amine copper complexes containing coupled pendent olefinic arms in atom transfer radical addition (ATRA) reactions
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Synthesis, characterization, X-ray crystallography analysis, and catalytic activity of bis(2-pyridylmethyl)amine copper complexes containing coupled pendent olefinic arms in atom transfer radical addition (ATRA) reactions

机译:含连接的侧链烯烃臂的双(2-吡啶甲基)胺铜配合物的合成,表征,X射线晶体学分析和催化活性在原子转移自由基加成(ATRA)反应中

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The synthesis, characterization, and catalytic activity of bis(2-pyridylmethyl)amine (BPMA) copper complexes incorporating olefinic pendent arms are reported. Four copper(I) and four copper(II) complexes were synthesized employing four different counterions [chloride (Cl-), perchlorate (ClO4-), trifluoromethanesulfonate (CF3SO3-), and tetraphenylborate (BPh4-)]. The counterions used ranged from coordinating (Cl-) to non-coordinating (BPh4-), producing different coordination modes in respective complexes. Solid state results obtained for the copper(I) complex incorporating the non-coordinating (BPh4-) counterion displayed an associative bond between the metal center and the C=C group in the olefinic arm of a neighboring complex. This interaction led to augmentation of the C=C bond due to back bonding from the metal center. Five solid state structures were obtained for the copper(II) complexes with two also displaying intermolecular associative bonding between olefinic pendent arms and the metal center. X-ray crystallography studies showed that the olefinic arm motifs incorporated were hemi-labile. Solution studies indicated that the copper complexes had some inherent reducing power and could be potential candidates for use as catalysts in atom transfer radical processes. However, only moderate conversions and yields were obtained in atom transfer radical addition (ATRA) reaction studies performed utilizing the copper complexes due to the presence of a competing reaction. (C) 2016 Elsevier Ltd. All rights reserved.
机译:报道了结合有烯烃侧链的双(2-吡啶基甲基)胺(BPMA)铜配合物的合成,表征和催化活性。使用四种不同的抗衡离子[氯化物(Cl-),高氯酸盐(ClO4-),三氟甲磺酸盐(CF3SO3-)和硼酸四苯酯(BPh4-)]合成了四种铜(I)和四种铜(II)配合物。使用的抗衡离子范围从配位(Cl-)到非配位(BPh4-),在各自的配合物中产生不同的配位模式。掺入非配位(BPh4-)抗衡离子的铜(I)配合物获得的固态结果显示,金属中心与相邻配合物的烯烃臂中的C = C基团之间具有缔合键。由于金属中心的反向键合,这种相互作用导致C = C键的增加。获得了铜(II)配合物的五个固态结构,其中两个还显示了烯烃垂臂和金属中心之间的分子间缔合键。 X射线晶体学研究表明,所结合的烯烃臂基序是半不稳定的。溶液研究表明,铜络合物具有一定的固有还原能力,可以作为原子转移自由基工艺中的催化剂。但是,由于存在竞争反应,在利用铜配合物进行的原子转移自由基加成(ATRA)反应研究中仅获得了中等的转化率和产率。 (C)2016 Elsevier Ltd.保留所有权利。

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