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螺吡喃作为分子开关和偶联体的构筑单元的合成。

Synthesis of spiropyrans as building blocks for molecular switches and dyads.

机构信息

University of Regensburg, Institute for Organic Chemistry, 93053 Regensburg, Germany.

出版信息

J Org Chem. 2010 Apr 16;75(8):2752-5. doi: 10.1021/jo100309r.

Abstract

The synthesis of spiropyrans was improved significantly with use of ultrasonic radiation. To show the broad applicability of this methodology a range of spiropyrans were prepared which are equipped with iodo, hydroxyl, ethinyl, or azido groups as potential building blocks for conjugation to functional pi-systems or biopolymers. Representatively, the conjugation chemistry was demonstrated for the preparation of spiropyran conjugates with pyrene, perylene, and nile red via the "click"-type cycloaddition. These molecular dyads were characterized by optical spectroscopy.

摘要

超声辐射显著改善了螺吡喃的合成。为了展示这种方法的广泛适用性,制备了一系列带有碘、羟基、乙炔基或叠氮基的螺吡喃,这些基团可以作为与功能π体系或生物聚合物进行共轭的潜在构建块。代表性的是,通过“点击”型环加成反应,展示了螺吡喃与芘、苝和尼罗红的共轭化学。这些分子偶联物通过光谱光学特性进行了表征。

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