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Rationalization of Supramolecular Chirality in a Bisporphyrin System

机译:双卟啉体系中超分子手性的合理化

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摘要

Supramolecular chirality is a growing multidisciplinary field of modern research and attracts much attention from the scientific community because of its vital importance for various natural processes and for its attractive possibilities for new smart technologies.Of the vast number of host-guest and self-associated systems,supramolecular assemblies based on porphyrin chromophores are of particular interest for in-depth investigation and potential application as a consequence of them having specific and well-suited physicochem-ical and spectroscopic properties.However,it is apparent that effective control of any functional system rests upon the comprehensive understanding of the detailed operative mechanisms and the corresponding driving forces.In the case of porphyrin-based supramolecular chiral assemblies (particularly,containing two or more porphyrins) there are two major factors which make such studies an arduous task:the dynamic nature of noncovalent assemblies and the complex electronic structure of these pigments as a consequence of the existence of several differently oriented electronic transitions.
机译:超分子手性是现代研究的一个多学科领域,由于其对于各种自然过程的重要意义以及对新智能技术的诱人可能性,因此引起了科学界的广泛关注。在众多主机和自相关系统中,基于卟啉发色团的超分子组装,由于它们具有特定且非常适合的物理化学和光谱性质,因此对于深入研究和潜在应用特别感兴趣。但是,显然,对任何功能系统的有效控制都取决于在全面了解详细的操作机理和相应的驱动力之后。对于以卟啉为基础的超分子手性组装体(特别是包含两种或更多种卟啉),有两个主要因素使这类研究成为一项艰巨的任务:动态性共价装配体和复杂元素这些颜料的电子结构是由于存在几种不同取向的电子跃迁而导致的。

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