meso-Aryl substituted stable unorthodox 5,10-porphodimethenes with α,β and β,β-Nmethyl pyrrole connectivities: synthesis and spectroscopic, solid state and theoretical characterization.
IR@CSIR-CFTRI
View Archive InfoField | Value | |
Relation |
http://ir.cftri.com/14641/
https://doi.org/10.1039/c9ob01062a |
|
Title |
meso-Aryl substituted stable unorthodox 5,10-porphodimethenes with α,β and β,β-Nmethyl pyrrole connectivities: synthesis and spectroscopic, solid state and theoretical characterization. |
|
Creator |
Nyancy, Halder
Sangeetha, Mohandas Usharani, D. Harapriya, Rath |
|
Subject |
24 Organic Chemistry
|
|
Description |
A concise and convenient synthetic methodology leading to an unambiguous isolation of two hitherto unknown highly stable single conformers of meso-aryl substituted unorthodox 5,10-porphodimethenes has been developed by the inclusion of N-methyl pyrrole units with α,β and β,β-linkages into the core of heterocyclic macrocycles. |
|
Date |
2019
|
|
Type |
Article
PeerReviewed |
|
Format |
pdf
|
|
Language |
en
|
|
Identifier |
http://ir.cftri.com/14641/1/Org.%20Biomol.%20Chem.%2C%202019.pdf
Nyancy, Halder and Sangeetha, Mohandas and Usharani, D. and Harapriya, Rath (2019) meso-Aryl substituted stable unorthodox 5,10-porphodimethenes with α,β and β,β-Nmethyl pyrrole connectivities: synthesis and spectroscopic, solid state and theoretical characterization. Organic and Biomolecular Chemistry, 17. pp. 6131-6135. |
|