129835-71-8Relevant academic research and scientific papers
A dendrimer chiroptical switch based on the reversible intramolecular photoreaction of anthracene and benzene rings
Liu, Wenjie,Cao, Derong,Peng, Jinan,Zhang, Hong,Meier, Herbert
scheme or table, p. 1896 - 1901 (2011/04/12)
A series of Frechet-type dendrimers with 9-benzyloxymethylanthracene cores were synthesized and characterized. The chiral source for the dendrimers was an (S)-2-methyl-1-butoxy group in the 3-position of the benzene ring. Irradiation at 366 nm of a dilute
Dendrimer analogues of linear molecules to evaluate energy and charge-transfer properties
Nantalaksakul, Arpornrat,Dasari, Raghunath Reddy,Ahn, Tai-Sang,Al-Kaysi, Rabih,Bardeen, Christopher J.,Thayumanavan
, p. 2981 - 2984 (2007/10/03)
We have designed and synthesized difunctionalized dendrimers containing two donors in the periphery and an acceptor at the core to serve as scaffolds for comparison with linear analogues to investigate the advantage of dendritic scaffolds for energy and c
Synthesis of difunctionalized dendrimers: An approach to main-chain poly(dendrimers)
Ganesh, Renuka N.,Shraberg, Joshua,Sheridan, Patrick G.,Thayumanavan
, p. 7217 - 7220 (2007/10/03)
Synthesis of benzyl ether dendrimers that are difunctionalized at their peripheries are described. These dendrimers should form the basis for a new class of main-chain dendritic polymers. The steric protection afforded at higher generation during the synt
Polymers with Controlled Molecular Architecture: Control of Surface Functionality in the Synthesis of Dendritic Hyperbranched Macromolecules using the Convergent Approach
Wooley, Karen L.,Hawker, Craig J.,Frechet, Jean M. J.
, p. 1059 - 1076 (2007/10/02)
The synthesis of unsymmetrically or non-uniformly surface-functionalized dentritic macromolecules using a stepwise convergent-growth approach is described.By stepwise alkylation of the monomer unit, 3,5-dihydroxybenzyl alcohol, with unsubstituted and subs
