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Synthesis and applications of novel imidazole and benzimidazole based sulfonic acid group functionalized Brönsted acidic ionic liquid catalysts

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dc.contributor.author Kore, R.
dc.contributor.author Srivastava, R.
dc.date.accessioned 2016-05-13T06:35:10Z
dc.date.available 2016-05-13T06:35:10Z
dc.date.issued 2016-05-13
dc.identifier.uri http://localhost:8080/xmlui/handle/123456789/28
dc.description.abstract In 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.iso en_US en_US
dc.subject Brönsted Acidic Ionic Liquids en_US
dc.subject Sulfonic Acid Functionalized Ionic Liquids en_US
dc.subject Multi-component Coupling Reactions en_US
dc.subject Hammett Acidity en_US
dc.subject Theoretical Studies en_US
dc.title Synthesis and applications of novel imidazole and benzimidazole based sulfonic acid group functionalized Brönsted acidic ionic liquid catalysts en_US
dc.type Article en_US


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