Publication | Closed Access
One “Click” to Access Push–Triazole–Pull Fluorophores Incorporating a Pyrimidine Moiety: Structure–Photophysical Properties Relationships
35
Citations
39
References
2013
Year
EngineeringHeterocyclicPhotochemistryAccess Push–triazole–pull FluorophoresNatural SciencesMolecular BiologyFluorous SynthesisOrganic ChemistryTriazole RingClick ChemistryChemistryPyrimidine MoietyHeterocycle ChemistryPhotophysical PropertyStructure–photophysical Properties RelationshipsBiomolecular EngineeringHuisgen 1,3‐Dipolar
Abstract Using copper‐catalysed Huisgen 1,3‐dipolar cycloaddition, we describe the synthesis of new A‐π‐D compounds containing a pyrimidine moiety as π‐acceptor (A) and various para ‐substituted benzene rings as donors (D). Structure–photophysical properties relationships revealed the triazole ring to be a better π‐conjugated linker than the triple bond.
| Year | Citations | |
|---|---|---|
Page 1
Page 1