Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.
ACS Nano. 2012 Jan 24;6(1):802-9. doi: 10.1021/nn2042797. Epub 2011 Dec 29.
Asymmetric assembly of nanomaterials has attracted broad interests because of their unique anisotropic properties that are different from those based on the more widely reported symmetric assemblies. Despite the potential advantages, programmable fabrication of asymmetric structure in nanoscale remains a challenge. We report here a DNA-directed approach for the assembly of asymmetric nanoclusters using Janus nanoparticles as building blocks. DNA-functionalized spherical gold nanoparticles (AuNSs) can be selectively attached onto two different hemispheres of DNA-functionalized Janus nanoparticle (JNP) through DNA hybridization. Complementary and invasive DNA strands have been used to control the degree and reversibility of the assembly process through programmable base-pairing interactions, resulting in a series of modular and asymmetric nanostructures that allow systematic study of the size-dependent assembly process. We have also shown that the attachment of the AuNSs onto the gold surface of the Janus nanoparticle results in red shifting of the UV-vis and plasmon resonance spectra.
由于具有不同于基于更广泛报道的对称组装的独特各向异性性质,纳米材料的不对称组装引起了广泛的关注。尽管具有潜在的优势,但在纳米尺度上可编程制造不对称结构仍然是一个挑战。我们在这里报道了一种使用 Janus 纳米粒子作为构建块组装不对称纳米簇的 DNA 导向方法。通过 DNA 杂交,DNA 功能化的球形金纳米粒子(AuNSs)可以选择性地附着在 DNA 功能化的 Janus 纳米粒子(JNP)的两个不同半球上。互补和侵入性 DNA 链已被用于通过可编程碱基配对相互作用控制组装过程的程度和可逆性,从而形成一系列模块化和不对称的纳米结构,允许对尺寸依赖性组装过程进行系统研究。我们还表明,AuNSs 附着在 Janus 纳米粒子的金表面上导致 UV-vis 和等离子体共振光谱的红移。