Related Experiment Video
Updated: Jun 19, 2025

Synthesis of pH Dependent Pyrazole, Imidazole, and Isoindolone Dipyrrinone Fluorophores using a Claisen-Schmidt Condensation Approach
Published on: June 10, 2021
Synthesis, Photophysical and Electrochemical Properties of Spiro-Phosphonium Compounds
Peng Zhao1, Tong Li1,2, Donghui Wei1
1College of Chemistry, International Phosphorus Laboratory, Zhengzhou University, Zhengzhou 450001, China.
Abstract:
A series of spiro-phosphonium compounds have been synthesized by copper-mediated coupling reaction of phosphacyclic compounds with alkynes. Their photophysical properties are tuned by varying substituents and exhibit different luminescent colors from blue to green, and finally, yellow. The fluorescence quantum efficiency of diethyl spiro-xanthenebenzophosphole 3aa in solid and liquid states reached 31% and 76%, respectively. Diphenyl spiro-xanthenebenzophosphole 3ad displayed relatively low cytotoxicity toward lung cancer cells A549 and was able to effectively penetrate the cell membrane and maintain strong staining. Moreover, density functional theory (DFT) and time-dependent DFT calculations have been performed to explore the origin of their photophysical properties.
Related Concept Videos
Variables Affecting Phosphorescence and Fluorescence
Photoluminescence: Fluorescence and Phosphorescence
A pair of electrons in a...
Photoluminescence: Applications
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Hybridization of Atomic Orbitals II
Electrophilic Addition to Alkynes: Halogenation
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.

