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将自旋和氧化还原不稳定的金属中心组织成 Langmuir 和 Langmuir-Blodgett 膜。

Organization of spin- and redox-labile metal centers into Langmuir and Langmuir-Blodgett films.

机构信息

Department of Chemistry, University of Fribourg, Chemin du Musee 9, CH-1700, Fribourg, Switzerland.

出版信息

Dalton Trans. 2010 May 21;39(19):4508-16. doi: 10.1039/b926023d.

Abstract

New sal₂(trien) ligands that contain alkoxy substituents of various length in meta position of the phenolate entities were coordinated to electronically and magnetically active iron(III) and cobalt(III) centers. The electrochemical and spectroscopic properties of these amphiphilic complexes are virtually unaffected upon alteration of the alkoxy substituents, thus providing a system in which the physical behavior and the metal-centered chemical activity can be tailored independently. The amphiphilic character has been exploited for preparing Langmuir monolayers at the air-water interface and for constructing Langmuir-Blodgett films, hence allowing for hierarchical assembling of electronically and magnetically active systems. While Langmuir films were stable, transfer onto solid supports was limited, which restricted the magnetic analysis of the Langmuir-Blodgett assemblies.

摘要

新型 sal₂(trien)配体,在邻位酚盐单元中具有不同长度的烷氧基取代基,与具有电子和磁活性的铁(III)和钴(III)中心配位。这些两亲性配合物的电化学和光谱性质几乎不受烷氧基取代基变化的影响,从而提供了一个可以独立调整物理行为和金属中心化学活性的体系。两亲性特征已被用于在气-水界面制备 Langmuir 单分子层和构建 Langmuir-Blodgett 膜,从而允许电子和磁活性系统的分级组装。虽然 Langmuir 膜是稳定的,但转移到固体载体上是有限的,这限制了 Langmuir-Blodgett 组装体的磁性分析。

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