Sidhaye Deepti S, Kashyap Sudhir, Sastry Murali, Hotha Srinivas, Prasad B L V
Nanoscience Group, Materials Chemistry Division, and Combi Chem-Bio Resource Center, Division of Organic Chemistry: Synthesis, National Chemical Laboratory, Pune 411 008, India.
Langmuir. 2005 Aug 16;21(17):7979-84. doi: 10.1021/la051125q.
Photoresponsive gold nanoparticle networks were prepared by functionalizing them with azobenzene derivatives. A network can be formed when a linker molecule constituting the azobenzene moiety suitably derivatized on either side with gold surface sensitive groups such as thiols and amines is added to the nanoparticle solution. It is shown that the interparticle spacing in the networks could be controlled by the reversible trans-cis isomerization of the azobenzene moiety induced by UV and visible light, respectively. The photoinduced variation in the interparticle spacings is inferred by the changes in the optical spectra of the gold nanoparticles which display a red or blue shift in the surface plasmon resonance peak depending on a decrease or increase in the interparticle spacing, respectively. Transmission electron microscopy images are in consonance with the evidence from the optical spectra.
通过用偶氮苯衍生物对光响应性金纳米颗粒网络进行功能化处理来制备它们。当将构成偶氮苯部分且在两侧用硫醇和胺等对金表面敏感的基团进行适当衍生化的连接分子添加到纳米颗粒溶液中时,可以形成网络。结果表明,网络中的颗粒间间距可分别通过紫外光和可见光诱导的偶氮苯部分的可逆反式-顺式异构化来控制。颗粒间间距的光致变化可通过金纳米颗粒光谱的变化来推断,根据颗粒间间距的减小或增大,表面等离子体共振峰分别出现红移或蓝移。透射电子显微镜图像与光谱证据一致。