134881-72-4Relevant articles and documents
THE TEMPLATE-DIRECTED SYNTHESIS OF A ROTAXANE
Ashton, Peter R.,Grognuz, Michel,Slawin, Alexandra M. Z.,Stoddart, J. Frazer,Williams, David J.
, p. 6235 - 6238 (1991)
X-Ray crystallography, FABMS, and 1H and 13C NMR spectroscopy have all been employed in the characterization of a self-assembled rotaxane composed of (i) a polyether chain intercepted by a centrally-located ?-electron rich hydroquinol ring and terminat
Cu2+-induced blue shift of the pyrene excimer emission: A new signal transduction mode of pyrene probes
Yang, Jye-Shane,Lin, Che-Sheng,Hwang, Chung-Yu
, p. 889 - 892 (2001)
matrix presented A pentiptycene-bispyrenyl system (1) has been synthesized and investigated as a fluorescent chemosensor for metal ions. A novel blue shift along with an intensity enhancement of the pyrene excimer emission is observed for 1 in the presenc
One-Pot Synthesis of a Linear [4]Catenate Using Orthogonal Metal Templation and Ring-Closing Metathesis
Amir, Faheem,Barnes, Jonathan C.,Chang, Christy,Colley, Nathan D.,Fisher, Jeremy M.,Greene, Angelique F.,Li, Lei,Li, Ruihan,Li, Xuesong,Nosiglia, Mark A.
supporting information, (2020/08/12)
The efficient synthesis of well-defined, linear oligocatenanes possessing multiple mechanical bonds remains a formidable challenge in the field of mechanically interlocked molecules. Here, a one-pot synthetic strategy is described to prepare a linear [4]catenate using orthogonal metal templation between a macrocycle precursor, composed of terpyridine and phenanthroline ligands spaced by flexible glycol linkers, and a closed phenanthroline-based molecular ring. Implementation of two simultaneous ring-closing metathesis reactions after metal complexation resulted in the formation of three mechanical bonds. The linear [4]catenate product was isolated in 55% yield as a mixture of topological diastereomers. The intermediate metal complexes and corresponding interlocked products (with and without metals) were characterized by nuclear magnetic resonance, mass spectrometry, gel permeation chromatography, and UV-vis absorption spectroscopy. We envision that this general synthetic strategy may pave the way for the synthesis of higher order linear oligocatenates/catenanes with precise molecular weights and four or more interlocking molecular rings.
One-pot synthesis of cyclophane-type macrocycles using manganese(iii)- mediated oxidative radical cyclization
Ito, Yosuke,Tomiyasu, Yuichi,Kawanabe, Takahiro,Uemura, Keisuke,Ushimizu, Yuu,Nishino, Hiroshi
supporting information; scheme or table, p. 1491 - 1507 (2011/04/23)
Cyclophane-type macrocyclic compounds from 21 to 56 members having two fused dihydrofuran rings were synthesized by the manganese(iii)-mediated oxidation of terminal dienes with bis(3-oxobutanoate)s containing aromatics. The reaction detail, characterization and reaction pathways are described. The Royal Society of Chemistry 2011.
