Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan.
J Am Chem Soc. 2015 Apr 29;137(16):5610-7. doi: 10.1021/jacs.5b02617. Epub 2015 Apr 16.
Photocontrolled organocatalyzed living radical polymerization was conducted over a wide range of irradiation wavelengths (350-750 nm). The polymerization was induced and controlled at the desired wavelengths by exploiting suitable organic catalysts. This system was finely responsive to the irradiation wavelength; the polymerization was instantly switched on and off, and the polymerization rate was sensitively modulated by altering the irradiation wavelength. The polymer molecular weight and its distribution (M(w)/M(n) = 1.1-1.4) were well controlled for methacrylate monomers up to fairly high conversions in many cases. The monomer scope encompassed various functional methacrylates, and their block copolymers were obtained. The feasibility of such a wide range of wavelengths and the fine response to the wavelength are unprecedented features. As a unique application of the wavelength-responsive nature of this system, we demonstrated "one-pot" selective regulation of living radical polymerization and another type of polymerization (ring opening polymerization), where the regulation was achieved by simply altering the irradiation wavelength. Facile operation and applicability to a wide range of polymer designs are advantages of this polymerization.
在较宽的辐射波长范围(350-750nm)内进行了光控有机催化的活性自由基聚合。通过利用合适的有机催化剂,在所需的波长下诱导和控制聚合。该体系对辐射波长有很好的响应;通过改变辐射波长,可以快速开启和关闭聚合,并且聚合速率可以被灵敏地调节。在许多情况下,对于甲基丙烯酸酯单体,聚合物的分子量及其分布(M(w)/M(n)=1.1-1.4)可以得到很好的控制,直到达到相当高的转化率。单体范围包括各种功能甲基丙烯酸酯单体,并获得了它们的嵌段共聚物。这种宽波长范围的可行性和对波长的精细响应是前所未有的特点。作为该体系波长响应特性的一个独特应用,我们演示了“一锅法”选择性调节活性自由基聚合和另一种聚合(开环聚合),通过简单地改变辐射波长即可实现调节。这种聚合的优点是操作简单,适用于广泛的聚合物设计。