首页> 外文期刊>Chemistry: A European journal >Preparation and Crystal Structures of Manganese, Iron, and Cobalt Complexes of the Bis[di(2-pyridyl)methyl] amine (bdpma) Ligand and Its Oxidative Degradation Product 1, 3, 3-Tris (2-pyridyl)-3H-imidazo [1, 5-a]-pyridin-4-ium (tpip); Origin of the bd
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Preparation and Crystal Structures of Manganese, Iron, and Cobalt Complexes of the Bis[di(2-pyridyl)methyl] amine (bdpma) Ligand and Its Oxidative Degradation Product 1, 3, 3-Tris (2-pyridyl)-3H-imidazo [1, 5-a]-pyridin-4-ium (tpip); Origin of the bd

机译:双[二(2-吡啶基)甲基]胺(bdpma)配体及其氧化降解产物1、3、3-三(2-吡啶基)-3H-咪唑的锰,铁和钴配合物的制备和晶体结构[1,5-a]-吡啶-4-鎓(tpip);公元的起源

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摘要

The synthesis and structural characterization of manganese, iron, and cobalt complexes of bis [di(2-pyridyl)methyl] amine (bdpma) were investigated. The bdpma ligand can give rise to mono- or dimeric complexes. Moreover, bdpma can undergo oxidative degradation leading to 1, 3, 3-tris (2-pyridyl)-3H-imidazo [1, 5-a]pyridin-4-ium (tpip) or to starting materials used for the preparation of bdpma. During attempts to prepare manganese, iron, or cobalt complexes of the tpip ligand, two classes of compounds were obtained. The first class corresponded to the tpip cation with a simple exchange of counterion and the second class led to a new type of complex, which involved a modification of tpip and contained the N-(di(2-pyridyl) methoxymethyl) (di(2-pyridyl) imine) (dpmmdpi) ligand. This work has allowed us to understand the fragility of the bdpma ligand, which is due to the easily activated benzylic C-H bonds in the #alpha# position to the heteroatom.
机译:研究了双[二(2-吡啶基)甲基]胺(bdpma)的锰,铁和钴配合物的合成和结构表征。 bdpma配体可产生单或二聚体复合物。而且,bdpma可能会发生氧化降解,从而导致1,3,3-三(2-吡啶基)-3H-咪唑并[1,5-a]吡啶-4-鎓(tpip)或用于制备bdpma的原料。在尝试制备tpip配体的锰,铁或钴配合物期间,获得了两类化合物。第一类对应于tpip阳离子,具有简单的抗衡离子交换,第二类对应于新型的络合物,其中涉及tpip的修饰,并包含N-(二(2-吡啶基)甲氧基甲基)(di(2 -吡啶基)亚胺)(dpmmdpi)配体。这项工作使我们能够了解bdpma配体的脆弱性,这是由于杂原子在#alpha#位置的易活化苄基C-H键所致。

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