Hydrogenation and cleavage of dinitrogen to ammonia with a zirconium complex

Jaime A. Pool, Emil Lobkovsky, Paul J. Chirik

Research output: Contribution to journalArticle

398 Scopus citations

Abstract

Molecular nitrogen is relatively inert owing to the strength of its triple bond, nonpolarity and high ionization potential. As a result, the fixation of atmospheric nitrogen to ammonia under mild conditions has remained a challenge to chemists for more than a century. Although the Haber-Bosch process produces over 100 million tons of ammonia annually for the chemical industry and agriculture, it requires high temperature and pressure, in addition to a catalyst, to induce the combination of hydrogen (H2) and nitrogen (N2). Coordination of molecular nitrogen to transition metal complexes can activate and even rupture the strong N-N bond under mild conditions, with protonation yielding ammonia in stoichiometric and even catalytic yields. But the assembly of N-H bonds directly from H2 and N2 remains challenging: adding H2 to a metal-N 2 complex results in the formation of N2 and metal-hydrogen bonds or, in the case of one zirconium complex, in formation of one N-H bond and a bridging hydride. Here we extend our work on zirconium complexes containing cyclopentadienyl ligands and show that adjustment of the ligands allows direct observation of N-H bond formation from N2 and H2. Subsequent warming of the complex cleaves the N-N bond at 45 °C, and continued hydrogenation at 85 °C results in complete fixation to ammonia.

Original languageEnglish (US)
Pages (from-to)527-530
Number of pages4
JournalNature
Volume427
Issue number6974
DOIs
StatePublished - Feb 5 2004
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • General

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