Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/444
Title: 4,4,9,9-Tetraphenyl pyrroloindolizine: a structural analogue of calix[2] pyrrole
Authors: Gowri Sreedevi, K C
Ajesh P Thomas
Ramakrishnan, S
Salini, P S
Derry Holaday, M G
Reddy, M L P
Srinivasan, A
Keywords: Porphyrinoids
NMR spectroscopic studies
Anion Binding
Binuclear Subphthalocyanine
Issue Date: 2012
Publisher: RSC Publishing
Citation: Organic and Biomolecular Chemistry 10(18):3600-3605;2012
Abstract: Synthesis, spectral and structural characterization of a pyrroloindolizine derivative having structural similarity with calix[2]pyrrole is described. Here, two pyrrole rings are connected with two meso-carbon atoms having an N,α-linkage and an α,β-linkage to afford the smallest analogue in the calixpyrrole family. Detailed NMR spectroscopic studies along with single crystal X-ray analysis confirm the assigned structure of the molecule
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