Jump to main content
Jump to site search

Issue 124, 2015
Previous Article Next Article

Formation of unusual dithiaphlorins from condensation of 2,5-bis(arylhydroxymethyl)thiophene and pyrrole

Author affiliations

Abstract

The first example of an unusual 21,23-dithiaphlorin containing pyrrole and aryl groups at the sp3 meso carbon that is present between the pyrrole and thiophene rings was isolated from the condensation of 2,5-bis(arylhydroxymethyl) and pyrrole under mild acid catalyzed conditions. The crystal structure revealed that the macrocycle is significantly distorted because of the presence of the sp3 meso carbon.

Graphical abstract: Formation of unusual dithiaphlorins from condensation of 2,5-bis(arylhydroxymethyl)thiophene and pyrrole

Back to tab navigation

Supplementary files

Publication details

The article was received on 20 Oct 2015, accepted on 21 Nov 2015 and first published on 24 Nov 2015


Article type: Paper
DOI: 10.1039/C5RA21947G
Author version
available:
Download author version (PDF)
RSC Adv., 2015,5, 102765-102771

  •   Request permissions

    Formation of unusual dithiaphlorins from condensation of 2,5-bis(arylhydroxymethyl)thiophene and pyrrole

    R. Sharma, W. Lee and M. Ravikanth, RSC Adv., 2015, 5, 102765
    DOI: 10.1039/C5RA21947G

Search articles by author

Spotlight

Advertisements