Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9242
Title: CS-symmetric triarylborane substituted bisthiazole for selective detection of F−and CN−ions
Authors: Misra, Rajneesh
Keywords: anion;borane derivative;boron;bromide ion;chloride ion;cyanide ion;fluoride ion;iodide ion;nitrite;palladium;tetrabutylammonium;tetrahydrofuran;thiazole derivative;triethylamine;unclassified drug;anion sensing;Article;binding affinity;carbon nuclear magnetic resonance;catalyst;chemical phenomena;density functional theory;electron;fluorescence;limit of detection;proton nuclear magnetic resonance;quantum yield;Sonogashira reaction;synthesis
Issue Date: 2016
Publisher: Elsevier Ltd
Citation: Maragani, R., Reddy, T. S., & Misra, R. (2016). CS-symmetric triarylborane substituted bisthiazole for selective detection of F−and CN−ions. Tetrahedron Letters, 57(34), 3853-3857. doi:10.1016/j.tetlet.2016.07.051
Abstract: Triarylborane substituted bisthiazole 1 was designed and synthesized by the Sonogashira cross-coupling reaction for selective detection of F−and CN−ions in the presence of Cl−, Br−, I−and NO2 −anions. The detection limits for F−and CN−were found to be 5.7 × 10−6 M and 2.1 × 10−6 M, respectively. The time dependent density functional theory (TD-DFT) calculation at B3LYP on the bisthiazole triarylborane 1 was studied for F−and CN−ions. In the case of 1 Boron is electron deficient, the addition of F−ion should increase the electron density on Boron which was confirmed by electrostatic potential surfaces of bisthiazole triarylborane dyad 1, 1-F. © 2016 Elsevier Ltd
URI: https://doi.org/10.1016/j.tetlet.2016.07.051
https://dspace.iiti.ac.in/handle/123456789/9242
ISSN: 0040-4039
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

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