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Recently we found that the rotational barrier of N-(ortho-tert- butylphenyl)-2-quinolinone is higher than 10 kcal/mol in comparison to that of N-(ortho-tert-butylphenyl)-3,4-dihydro-2-quinolinone. The high rotational barrier of N-(ortho-tert-butylphenyl)-2-quinolinone was disclosed to be due to the rigid aromatic structure
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CCDC-901836 4g contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
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CCDC-901836 4g contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via http://www.ccdc.com.ac.uk/data-request/cif.
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