Please use this identifier to cite or link to this item: http://ir.niist.res.in:8080/jspui/handle/123456789/837
Title: 5, 5-Diaryldipyrromethanes: syntheses and anion binding properties
Authors: Gowri Sreedevi, K C
Ajesh P Thomas
Salini, P S
Ramakrishnan, S
Anju, K S
Holaday, M G D
Reddy, M L P
Suresh, C H
Srinivasan, A
Keywords: Bodipy dyes
Dipyrrolide ligands
Mesosubstituted porphyrins
One-step synthesis
N bond-cleavage
Grignard reagent
Anion binding
Dipyrromethane
Pyrrole-2-carbinol
Issue Date: 2011
Publisher: Elsevier
Citation: Tetrahedron Letters 52(45):5995-5999;09 Nov 2011
Abstract: A two-step synthesis of 5, 5-diaryldipyrromethanes in good yields is described. The adopted synthetic strategy can be used to tune the substituent at the meso-carbon very easily by choosing the Grignard reagent of interest. Further, the influence of the incorporation of various diaryl units at the mesa-carbon atom in the inherent anion binding affinities of the dipyrromethanes through hydrogen bonding was discussed.
URI: http://ir.niist.res.in:8080/jspui/handle/123456789/837
ISSN: 0040-4039
Appears in Collections:2011

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