157067-93-1Relevant articles and documents
A new photo switchable azobenzene macrocycle without thermal relaxation at ambient temperature
Eleya, Nadi,Ghosh, Souvik,Lork, Enno,Staubitz, Anne
supporting information, p. 82 - 87 (2021/01/15)
A new switchable azobenzene macrocyclic derivative has been prepared in 4 steps with an overall yield of 47%. This molecule shows photoisomerization between the E and Z isomers using light of 365 nm and 405 nm respectively. What differentiates this macroc
Template synthesis of helicates of a [2 + 2] tetraimine macrocycle: Crystal structure of the lead(II) perchlorate complex
Fenton, David E.,Matthews, Ray W.,McPartlin, Mary,Murphy, Brian P.,Scowen, Ian J.,Tasker, Peter A.
, p. 3421 - 3427 (2007/10/03)
The Schiff-base condensation of α,α′-bis(2-aminophenoxy)-o-xylene and pyridine-2,6-dicarbaldehyde produced mononuclear complexes of the same [2 + 2] cyclocondensation product L1 in the presence of divalent metal ions ranging in size from Mnsup
Stereochemistry of Crown Ethers I. Conformational and Dynamic Behaviour of N-Tosyl-Substituted Diaza Crown Ethers
Kleinpeter, E.,Gaebler, M.,Schroth, W.
, p. 380 - 386 (2007/10/02)
The variable temperature 1H and 13C NMR spectra of some N-tosyl diaza crown ethers have been obtained.They are discussed with respect to the preferred conformers of the crowns and the free energies of activation of the interconversional process of the large ring.Both the preferred conformers and the ring interconversional barriers have been found strongly dependent on the structure and the ring size of the studied compounds.KEY WORDS Variable-temperature 1H and 13C NMR spectra N-tosyl diaza crown ethers Crown conformation Free energies of activation.