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dc.contributor.authorKore, R.-
dc.contributor.authorSrivastava, R.-
dc.date.accessioned2016-05-13T06:35:10Z-
dc.date.available2016-05-13T06:35:10Z-
dc.date.issued2016-05-13-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/28-
dc.description.abstractIn this study, a variety of imidazole/benzimidazole based sulfonic acid group functionalized Brönsted acidic ionic liquids (BAILs) were synthesized. Catalytic activities of BAILs were assessed using multi-component coupling reactions. Catalytic activities of BAILs were high when compared with those of solid acid catalysts such as H-ZSM-5, H-BETA, and sulfonic acid functionalized SBA-15 catalysts. The Hammett acidity order determined from UV–visible spectroscopy of BAILs is consistent with their activity order observed in acid-catalyzed reactions. Theoretical studies demonstrate that the hydrogen bonding plays a key role in tuning the acidity of BAILs. Recycling experiments suggest that these novel BAILs can be reused without significant loss in catalytic activity. Novel BAILs offer several attractive features such as low cost, high catalytic activity, and recyclability.en_US
dc.language.isoen_USen_US
dc.subjectBrönsted Acidic Ionic Liquidsen_US
dc.subjectSulfonic Acid Functionalized Ionic Liquidsen_US
dc.subjectMulti-component Coupling Reactionsen_US
dc.subjectHammett Acidityen_US
dc.subjectTheoretical Studiesen_US
dc.titleSynthesis and applications of novel imidazole and benzimidazole based sulfonic acid group functionalized Brönsted acidic ionic liquid catalystsen_US
dc.typeArticleen_US
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