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3,5-双(三氟甲基)吡唑配体的铜和银加合物与有机铁化合物的络合特性。

Peculiarities of the complexation of copper and silver adducts of a 3,5-bis(trifluoromethyl)pyrazolate ligand with organoiron compounds.

机构信息

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Vavilov str. 28, 119991 Moscow, Russia.

出版信息

Inorg Chem. 2011 Apr 18;50(8):3325-31. doi: 10.1021/ic102132v. Epub 2011 Mar 15.

Abstract

Interaction of the copper, {[3,5-(CF(3))(2)Pz]Cu}(3), and silver, {[3,5-(CF(3))(2)Pz]Ag}(3), macrocycles [3,5-(CF(3))(2)Pz = 3,5-bis(trifluoromethyl)pyrazolate] with cyclooctatetraeneiron tricarbonyl, (cot)Fe(CO)(3), was investigated by IR and NMR spectroscopy for the first time. The formation of 1:1 complexes was observed at low temperatures in hexane. The composition of the complexes (1:1) and their thermodynamic characteristics in hexane and dichloromethane were determined. The π-electron system of (cot)Fe(CO)(3) was proven to be the sole site of coordination in solution and in the solid state. However, according to the single-crystal X-ray data, the complex has a different (2:1) composition featuring the sandwich structure. The complexes of ferrocene with copper and silver macrocycles have a columnar structure (X-ray data).

摘要

首次通过红外和核磁共振光谱法研究了铜、{[3,5-(CF(3))(2)Pz]Cu}(3)和银、{[3,5-(CF(3))(2)Pz]Ag}(3)大环与环辛四烯铁三羰基,(cot)Fe(CO)(3)的相互作用。在正己烷中,低温下观察到形成 1:1 配合物。在正己烷和二氯甲烷中确定了配合物(1:1)的组成及其热力学特性。证明(cot)Fe(CO)(3)的π-电子体系是溶液中和固态中配位的唯一位置。然而,根据单晶 X 射线数据,该配合物具有不同的(2:1)夹心结构组成。二茂铁与铜和银大环的配合物具有柱状结构(X 射线数据)。

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