Multiple threading of a triple-calix[6]arene host

التفاصيل البيبلوغرافية
العنوان: Multiple threading of a triple-calix[6]arene host
المؤلفون: Annunziata Soriente, Carmen Talotta, Patrizia Iannece, Margherita De Rosa, Carmine Gaeta, Roberta Ciao, Emanuele Vignola, Veronica Iuliano, Placido Neri
المصدر: Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2092-2104 (2019)
Beilstein Journal of Organic Chemistry
بيانات النشر: Beilstein Institut, 2019.
سنة النشر: 2019
مصطلحات موضوعية: Letter, Rotaxane, Chemistry, Organic Chemistry, lcsh:QD241-441, Crystallography, Multiple-threading, Pseudo[n]rotaxane, lcsh:Organic chemistry, Calixarene, Stereoisomers, Moiety, lcsh:Q, Stereoselectivity, Threading (protein sequence), lcsh:Science, Two-dimensional nuclear magnetic resonance spectroscopy
الوصف: The synthesis of the triple-calix[6]arene derivative 6 in which three calix[6]arene macrocycles are linked to a central 1,3,5-trimethylbenzene moiety is reported. Derivative 6 is able to give multiple-threading processes in the presence of dialkylammonium axles. The formation of pseudo[2]rotaxane, pseudo[3]rotaxane, and pseudo[4]rotaxane by threading one, two, and three, respectively, calix-wheels of 6 has been studied by 1D and 2D NMR, DOSY, and ESI-FT-ICR MS/MS experiments. The use of a directional alkylbenzylammonium axle led to the stereoselective formation of endo-alkyl pseudo[n]rotaxane stereoisomers.
تدمد: 1860-5397
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2878238876b5febe9a5f3818aea2237dTest
https://doi.org/10.3762/bjoc.15.207Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....2878238876b5febe9a5f3818aea2237d
قاعدة البيانات: OpenAIRE