Generic placeholder image

Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

One Pot Synthesis of 1,10-Phenanthroline-based Shape-Persistent Flouroscent Macrocycle Using Sonogashira Coupling

Author(s): Said Nadeem, Muhammad R. Shah, Qamar Ali and Zahid Hussain

Volume 12, Issue 7, 2015

Page: [504 - 510] Pages: 7

DOI: 10.2174/157017861207150708113303

Price: $65

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.

Keywords: Shape-persistent Macrocycles, Sonogashira Coupling of Aryl chlorides, 1, 10-phenanthroline, Fluorescent Macrocycles.

Graphical Abstract


Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy