335342-60-4Relevant academic research and scientific papers
Novel synthesis of macrocycles with 1,1′-binaphthalene-2,2′-diol using intramolecular oxidative coupling
Ito, Satoshi,Koizumi, Kazuya,Fukuda, Katsuhiko,Kameta, Naohiro,Ikeda, Tsukasa,Oba, Toru,Hiratani, Kazuhisa
, p. 8563 - 8566 (2006)
A new series of BINOL-based macrocycles with two phenolic protons have been synthesized via oxidative coupling reaction using CuCl(OH)-TMEDA.
EXPLOSIVES DETECTION MARKERS
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Page/Page column 10; 15; Sheet 12/16, (2008/06/13)
The present invention relates to a porphyrinogen based sensor having selective binding affinity for an explosive chemical. Upon binding of the target molecule, the porphyrinogen derivative undergoes a detectable adsorption and emission of electromagnetic
Tetrathiafulvalene-containing pseudorotaxanes formed between dibenzylammonium salts and crown ethers
Ashton, Peter R,Becher, Jan,Fyfe, Matthew C.T,Nielsen, Mogens Br?ndsted,Stoddart, J.Fraser,White, Andrew J.P,Williams, David J
, p. 947 - 956 (2007/10/03)
The synthesis of two tetrathiafulvalene (TTF) derivatives, one carrying arms incorporating four dibenzylammonium centers and the other encompassing two annulated crown ether rings - i.e., hydrogen bond donor and acceptor functions, respectively, is described. In the presence of macrocyclic polyethers - e.g., DB24C8 and BPP34C10 - and dibenzylammonium hexafluorophosphate, these two TTF derivatives form pseudorotaxanes as evidenced by 1H NMR spectroscopy, mass spectrometry, and differential pulse voltammetry.
