909389-75-9Relevant academic research and scientific papers
Coordination-driven self-assembly of metallodendrimers possessing well-defined and controllable cavities as cores
Yang, Hai-Bo,Hawkridge, Adam M.,Huang, Songping D.,Das, Neeladri,Bunge, Scott D.,Muddiman, David C.,Stang, Peter J.
, p. 2120 - 2129 (2007)
The design and self-assembly of novel cavity-cored metallodendrimers via noncovalent interactions are described. By employing [G0]-[G3] 120° ditopic donor linkers substituted with Frechet-type dendrons and appropriate rigid di-Pt(II) acceptor subunits, [G
Orthogonal Self-Assembly of a Two-Step Fluorescence-Resonance Energy Transfer System with Improved Photosensitization Efficiency and Photooxidation Activity
Jia, Pei-Pei,Xu, Lin,Hu, Yi-Xiong,Li, Wei-Jian,Wang, Xu-Qing,Ling, Qing-Hui,Shi, Xueliang,Yin, Guang-Qiang,Li, Xiaopeng,Sun, Haitao,Jiang, Yanrong,Yang, Hai-Bo
supporting information, p. 399 - 408 (2021/01/12)
During the past few decades, fabrication of multistep fluorescence-resonance energy transfer (FRET) systems has become one of the most attractive topics within supramolecular chemistry, chemical biology, and materials science. However, it is challenging t
Molecular architecture via coordination: Self-assembly of nanoscale hexagonal metallodendrimers with designed building blocks
Yang, Hai-Bo,Das, Neeladri,Huang, Feihe,Hawkridge, Adam M.,Muddiman, David C.,Stang, Peter J.
, p. 10014 - 10015 (2007/10/03)
The first self-assembly of nanoscale metallodendrimers that have a hexagonal cavity as a core via the directional-bonding approach is reported. All metallodendrimers were characterized by multinuclear NMR (1H and 31P), mass spectrome
