60317-39-7Relevant academic research and scientific papers
Solid-Phase Benzoylation of Phenols and Alcohols in Microwave Reactor: An Ecofriendly Protocol
Chakraborty, Suchandra,Saha, Ahana,Basu, Kaushik,Saha, Chandan
supporting information, p. 2331 - 2343 (2015/10/12)
An efficient solid-phase benzoylation of phenols and alcohols was developed under microwave irradiation. A stoichiometric amount of benzoyl chloride was sufficient to carry out the reaction. This benzoylation features short reaction time, good yields, and easy workup procedures. Furthermore, the scope of the reaction was extended to prepare 3,5-dinitrobenzoyl derivatives of alcohols.
Use of solvent to regulate the degree of polymerisation in weakly associated supramolecular oligomers
B?hring, Steffen,Kim, Dong Sub,Duedal, Troels,Lynch, Vincent M.,Nielsen, Kent A.,Jeppesen, Jan O.,Sessler, Jonathan L.
supporting information, p. 5497 - 5499 (2014/05/20)
Using a tetrathiafulvalene functionalised calix[4]pyrrole (TTF-C[4]P; 1) and alkyl diester-linked bis-dinitrophenols (2-4), it was found that the solvent polarity and linker length have an effect on the molecular aggregation behaviour. 2D 1H NO
Charge-transfer interactions for the fabrication of multifunctional viral nanoparticles
Hu, Jun,Wang, Peiyi,Zhao, Xia,Lv, Lin,Yang, Song,Song, Baoan,Wang, Qian
supporting information, p. 14125 - 14128 (2015/02/19)
A facile strategy to fabricate multifunctional viral nanoparticles was described by introducing charge-transfer interactions between a pyrenyl motif with dinitrophenyl and pyridinium-contained guest molecules. This journal is
Controlled self-assembly manipulated by charge-transfer interactions: From tubes to vesicles
Wang, Chao,Yin, Shouchun,Chen, Senlin,Xu, Huaping,Wang, Zhiqiang,Zhang, Xi
supporting information; experimental part, p. 9049 - 9052 (2009/02/08)
Transfer request: A self-assembled-supramolecular charge-transfer complex of 1-(11-oxo-11-pyren-1-ylmethoxy)undecyl)-pyridinium bromide (PYR) and ethane-1,2-diyl bis(3,5-dinitrobenzoate) (DNB) is shown to form vesicular aggregates in aqueous solution, in contrast to the tubular aggregates of pure PYR (see picture). A curvature-dependent mechanism for this change is proposed. (Figure Presented)
