Skip to content
2000
Volume 12, Issue 7
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

A rigid shape-persistent fluorescent macrocycle PhenMac was synthesized using Sonogashira coupling reaction and TIPS-decoupling in a single pot. 2,9-dichloro-1,10-phenanthroline was reacted with TIPS-protected diyne 2 in the presence of Pd(PPh3)2Cl2, CuI and TBAF at 100 °C. PhenMac was obtained as yellow fluorescent compound; characterized by NMR, ESI, MALDI-TOF, CHN, IR and UVvisible spectroscopy. In chloroform, PhenMac showed λex-max at 331 nm while λem-max was observed at 407 nm. Under UV light, PhenMac showed more fluorescence in CHCl3, ethanol, and DMF while the fluorescence was quenched in triethylamine. PhenMac will be used in various applications of [poly]catenanes, supramolecular chemistry and nanotechnology.

Loading

Article metrics loading...

/content/journals/loc/10.2174/157017861207150708113303
2015-08-01
2025-09-06
Loading full text...

Full text loading...

/content/journals/loc/10.2174/157017861207150708113303
Loading
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test