Synthesis, optical, and structural properties of bisphenol-bridged aromatic cyclic phosphazenes
Bünyemin ÇoŞut1, Burcu TopaloĞlu Aksoy1, Süreyya Oğuz TÜmay1
1Department of Chemistry, Faculty of Science, Gebze Technical University, Gebze, Kocaeli Turkey.
Abstract:
Phenoxy- and naphthoxy-substituted bisphenol-bridged cyclic phosphazenes were synthesized in 2 steps and their thermal, photophysical, and electrochemical properties were investigated. The structures of the cyclic phosphazene compounds were determined by ESI-MS mass spectrometry and 1 H, 13 C, and 31 P NMR spectroscopies. The photophysical studies of phenoxy- and naphthoxy-substituted bridged cyclophosphazenes were investigated by means of absorption and fluorescence spectroscopies in different solvents. Thermal and electrochemical properties of the target compounds were also studied. Furthermore, the excimer emissions through intramolecular interactions in solution and in solid state were investigated by fluorescence spectroscopy and the theoretical calculations were performed in detail using DFT.
Related Concept Videos
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry
Criteria for Aromaticity and the Hückel 4n + 2 Rule
For the first time, Eric Hückel, a German chemical physicist, derived a set of structural features for a compound to be classified as aromatic. This is now known as Hückel’s rule or the 4n +...
Frost Circles for Different Conjugated Systems
Five-Membered Heterocyclic Aromatic Compounds: Overview
Aromatic Hydrocarbon Anions: Structural Overview
Due to the absence of continuous...

![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)
