75507-14-1Relevant academic research and scientific papers
Preparation and decomposition of potassium alkalide-lipophilic crown ether complexes in tetrahydrofuran
Grobelny, Zbigniew,Stolarzewicz, Andrzej,Morejko-Buz, Barbara,Bartsch, Richard A.,Yamato, Kazuhiro,Fernandez, Fernando A.,Maercker, Adalbert
, p. 7807 - 7812 (2007/10/03)
Cyclohexano-15-crown-5, cyclohexano-18-crown-6, dicyclohexano-15-crown-5, and dicyclohexano-18-crown-6, but not dicylohexano-16-crown-5, in THF dissolve potassium metal to form dark blue potassium alkalide solutions at ambient temperature. On standing, the potassium alkalide complexes decompose and the solutions turn colorless at differing rates. Identification of the products provides insight into the decomposition mechanism.
STEREODESIGN OF CROWN ETHERS. I. SYNTHESIS AND (13)C NMR STUDY OF TRANS- CYCLOHEXANOCROWN ETHERS
Samoshin, V. V.,Zelenkina, O. A.,Subbotin, O. A.,Sergeev, N. M.,Zefirov, N. S.
, p. 413 - 418 (2007/10/02)
A series of trans-cyclohexanocrown ethers were synthesized by the intermolecular cyclization of polyethylene glycol trans-2-hydroxycyclohexyl ethers with the ditosyl derivatives of polyethylene glycols.A complete assignment of the signals in the (13)C NMR spectra was made for the obtained compounds.
Synthesis of Substituted Crown Ethers from Oligoethylene Glycols
Ikeda, Isao,Yamamura, Shingo,Nakatsuji, Yohji,Okahara, Mitsuo
, p. 5355 - 5358 (2007/10/02)
A convenient synthetic method for preparing 12-crown-4, 15-crown-5, 18-crown-6, and 21-crown-7 bearing various substituents by intramolecular cyclization of the corresponding substituted oligoethylene glycols in high yields is described.Substituents include modifiable pendent groups such as phenyl and hydroxymethyl, as well as various alkyl groups.Stability constants for the new substituted crown ethers with sodium and potassium ions in methanol were determined by potentiometric titration.The absolute effect of pendent groups on stability constants was insignificant.
