A theoretical study on the phosgenation of methylene diphenyl diamine (MDA)

R. Zsanett Boros, Tamás Koós, Cheikh Wafaa, Károly Nehéz, László Farkas, B. Viskolcz, Milán Szőri

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

G3MP2B3 calculations were used to investigate the mechanism of the phosgenation reactions of 4,4′-methylenedianiline (MDA) resulted in the formation of methylene diphenyl diisocyanate (MDI). Due to o-dichlorobenzene solvation the reaction barriers are dramatically reduced compared to the gas phase reaction mechanism. The mechanisms of the ‘phosgenations first’ and ‘stepwise phosgenations’ are energetically compared. Standard enthalpy of formation for MDI (14.8 ± 5.2 kJ/mol) and the group additivity increments for OCN and NHCOCl groups linked to phenyl ring are proposed (Δf,iH0(-NCO) = −61.2 kJ/mol and Δf,iH0(-NHCOCl) = −195.0 kJ/mol). A thermodynamic stabile charge separated amine hydrochloride intermediate can mask the amine toward phosgene.

Original languageEnglish
Pages (from-to)568-576
Number of pages9
JournalChemical Physics Letters
Volume706
DOIs
Publication statusPublished - Aug 16 2018

ASJC Scopus subject areas

  • Physics and Astronomy(all)
  • Physical and Theoretical Chemistry

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