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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.

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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.