143032-08-0Relevant articles and documents
Synthesis, characterization and aggregation induced enhanced emission properties of tetraaryl pyrazole decorated cyclophosphazenes
Mukundam, Vanga,Dhanunjayarao, Kunchala,Mamidala, Ramesh,Venkatasubbaiah, Krishnan
, p. 3523 - 3530 (2016)
A series of cyclotriphosphazenes N3P3(O-C6H4-C3N2-(C6H5)3)6 (3), N3P3(O2C12H8)(O-C6/
AIEE phenomenon: Tetraaryl vs. triaryl pyrazoles
Mukherjee, Sayani,Salini,Srinivasan,Peruncheralathan
supporting information, p. 17148 - 17151 (2015/12/05)
Tetraarylpyrazoles are synthesized from commercially available materials in three steps and found to exhibit Aggregation Induced Emission Enhancement (AIEE) characteristics. Removing one aryl unit from tetraarylpyrazole leads to Aggregation Caused Quenching (ACQ), thus the number of aryl groups plays an important role in exploring such a phenomenon.
Correlation of spectroscopically determined ligand donor strength and nucleophilicity of substituted pyrazoles
Bernhammer, Jan Christopher,Huynh, Han Vinh
supporting information; experimental part, p. 8600 - 8608 (2012/10/07)
The relative ligand donor strengths of 10 pyrazole-derived ligands has been determined with great accuracy, making use of the interdependence between the donor strength of the co-ligand and the 13C NMR chemical shift of the iPr2-bimy carbene signal in trans-[PdBr2( iPr2-bimy)L] complexes (iPr2-bimy = 1,3-diisopropylbenzimidazolin-2-ylidene; L = pyrazole-derived ligand). Even subtle variations in the substitution pattern of the pyrazole backbone up to three bonds away from the coordinating nitrogen could be detected reliably using this methodology. Alkylation experiments conducted on the pyrazoles using electrophiles of varied reactivity (ethyl bromide, ethyl iodide, and trimethyloxonium tetrafluoroborate) served as a benchmark to rank the pyrazoles in three groups of gradually increasing nucleophilicity, which correlated well with their determined donor strength.