Amination of ketene: A theoretical study

Kuang-Sen Sung, Thomas T. Tidwell

Research output: Contribution to journalArticle

55 Citations (Scopus)

Abstract

The reactions of NH3, (NH3)2, and (H3N·H2O) with ketene have been studied by ab initio calculations. Attack by the dimer (NH3)2 or by (H3N·H2O) through six-membered cyclic transition states is found to be favored, with a preference of 12.8 kcal/mol for initial addition of (NH3)2 to the C=O bond of the ketene giving the enol amide, as compared to initial addition to the C=C bond to give the more stable amide directly. These results ate in contrast to previous theoretical studies for the reaction of monomeric NH3 with ketene, in which direct addition to the C=C bond was reported to be favored, and for the reaction of ketene with (H2O)2, in which addition to the C=O bond is calculated to be only 1.9 kcal/mol more favorable than addition to the C=C bond. The barrier via 10(ts) for the NH3- catalyzed rearrangement of the enol amide/NH3 complex 6 to the amide is 16.5 kcal/mol above that of 6, consistent with the experimental observation of an intermediate in ketene amination, and the barrier for reversion of 6 to the reactant complex 5a is 4.0 kcal/mol lower than that for amide formation via 10(ts), suggesting the initial amination may be reversible. These results demonstrate that previous theoretical calculations of ketene amination used inadequate levels of theory. The structure of the zwitterion CH2=C(O- )NMe3+ (14) from reaction of ketene with NMe3 has also been calculated, and in the gas phase this reaction is calculated to be exothermic by only 0.6 kcal/mol.

Original languageEnglish
Pages (from-to)3043-3048
Number of pages6
JournalJournal of the American Chemical Society
Volume120
Issue number13
DOIs
Publication statusPublished - 1998 Apr 8

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)
  • Biochemistry
  • Colloid and Surface Chemistry

Fingerprint Dive into the research topics of 'Amination of ketene: A theoretical study'. Together they form a unique fingerprint.

  • Cite this