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A selenium-coordinated palladium(ii) trans-dichloride molecular rotor as a catalyst for site-selective annulation of 2-arylimidazo[1,2-a]pyridines

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dc.contributor.author Kumar, Anil
dc.date.accessioned 2021-10-14T13:10:07Z
dc.date.available 2021-10-14T13:10:07Z
dc.date.issued 2020
dc.identifier.uri https://pubs.rsc.org/en/content/articlelanding/2020/cc/d0cc03599h
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2815
dc.description.abstract This report describes the synthesis of a new class of secondary interaction (SeCH⋯Cl)-controlled molecular rotor having a Cl–Pd–Cl rotor spoke attached onto a Se–Pd–Se axle. NMR data acquired at various temperatures established ΔG‡298K/ΔG‡350K values of 15.5 and 17.2 kcal mol−1 for a roughly 4.5 Å-long rotor. The molecular rotor showed excellent catalytic activity with reverse regioselectivity for annulation of 2-arylimidazo[1,2-a]pyridines (yields: ∼53–78%) with only 1.5 mol% catalyst loading. en_US
dc.language.iso en en_US
dc.publisher RSC en_US
dc.subject Chemistry en_US
dc.subject Selenium-coordinated en_US
dc.title A selenium-coordinated palladium(ii) trans-dichloride molecular rotor as a catalyst for site-selective annulation of 2-arylimidazo[1,2-a]pyridines en_US
dc.type Article en_US


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