Repository logo
 

Synthesis and Properties of Tetra-aryl Azobispyrroles

dc.contributor.authorSteve O. Sequeira
dc.contributor.authorRoberto M. Diaz-Rodriguez
dc.contributor.authorMmasinachi Atansi
dc.contributor.authorJames W. Hilborn
dc.contributor.authorAdil Alkaş
dc.contributor.authorRosinah Liandrah Gapare
dc.contributor.authorMadeleine Dearden
dc.contributor.authorEm C. Sullivan
dc.contributor.authorEmily B. Brown
dc.contributor.authorKatherine N. Robertson
dc.contributor.authorAlison Thompson
dc.date.accessioned2025-07-29T18:21:18Z
dc.date.available2025-07-29T18:21:18Z
dc.date.issued2025
dc.description.abstractAn unprecedented azobispyrrole framework is introduced, wherein two aryl-substituted pyrroles are joined by an azo (–N[double bond, length as m-dash]N–) linkage. Functionalisation was demonstrated via pyrrolic N-methylation and by –BF2 complexation using the coordinating abilities of the pyrrolic and azo nitrogen atoms. Control of co-planarity enables tunability with maximal absorption and emission spanning almost 300 nm.
dc.identifier.citationAlkaş, Adil & Diaz-Rodriguez, Roberto & Sequeira, Steve & Hilborn, James & Atansi, Mmasinachi & Sullivan, Em & Brown, Emily & Gapare, Rosinah & Mutus, Bulent & Robertson, Katherine & Thompson, Alison. (2025). Introducing the substituted azobispyrrole framework: synthesis and properties. Chemical communications (Cambridge, England). 10.1039/d5cc02884a.
dc.identifier.urihttps://hdl.handle.net/10222/85249
dc.publisherRoyal Society of Chemistry
dc.relation.ispartofChemical Communications
dc.titleSynthesis and Properties of Tetra-aryl Azobispyrroles

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
8manuscript azo full clean.pdf
Size:
753.96 KB
Format:
Adobe Portable Document Format

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
2.12 KB
Format:
Item-specific license agreed upon to submission
Description:

Collections