4.6 Article

Research frontiers in the chemistry of Criegee intermediates and tropospheric ozonolysis

期刊

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 16, 期 5, 页码 1704-1718

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cp52842a

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资金

  1. Natural Environment Research Council, U.K.
  2. Division of Chemical Sciences, Geosciences, and Biosciences, the Office of Basic Energy Sciences, U.S. Department of Energy
  3. National Nuclear Security Administration [DE-AC04-94-AL85000]
  4. Institute for Advanced Studies of the University of Bristol
  5. Natural Environment Research Council [NE/G01972X/1, NE/J009008/1, NE/K005316/1, NE/K004905/1, NE/I014381/1, NE/K01501X/1] Funding Source: researchfish
  6. NERC [NE/I014381/1, NE/K01501X/1, NE/K005316/1, NE/K004905/1, NE/G01972X/1, NE/J009008/1] Funding Source: UKRI

向作者/读者索取更多资源

The chemistry of carbonyl oxides, known as Criegee intermediates, is central to many aspects of tropospheric chemistry. For decades it has been known that these reactive species, whose electronic structure contains zwitterionic and biradical character, are formed in the ozonolysis of alkenes. However it is only recently that direct measurements of their reaction kinetics have become possible. In this perspective we describe the most recent progress in understanding the reactivity of these historically elusive molecules, explore the atmospheric chemistry implications of new experimental discoveries, and propose important new areas for investigation.

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