4.8 Article

High-Pressure Synthesis of a Pentazolate Salt

Journal

CHEMISTRY OF MATERIALS
Volume 29, Issue 2, Pages 735-741

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.6b04538

Keywords

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Funding

  1. Defense Threat Reduction Agency [HDTRA1-12-1-0023]
  2. U.S. Department of Energy by Lawrence Livermore National Security, LLC [DE-AC52- 07NA27344]
  3. U.S. NSF [EAR-0622171, DMR-1231586]
  4. DOE Geosciences [DE-FG02-94ER14466]
  5. DOE-BES [DE-AC02-06CH11357]
  6. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy [DE-AC02-05CH11231]
  7. Direct For Mathematical & Physical Scien
  8. Division Of Materials Research [1231586] Funding Source: National Science Foundation

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The pentazolates, the last all-nitrogen members of the azole series, have been notoriously elusive for the last hundred years despite enormous efforts to make these compounds in either gas or condensed phases. Here, we report a successful synthesis of a solid state compound consisting of isolated pentazolate anions N-5(-), which is achieved by compressing and laser heating cesium azide (CsN3) mixed with N-2 cryogenic liquid in a diamond anvil cell. The experiment was guided by theory, which predicted the transformation of the mixture at high pressures to a new compound, cesium pentazolate salt (CsN5). Electron transfer from Cs atoms to N-5 rings enables both aromaticity in the pentazolates as well as ionic bonding in the CsN5 crystal. This work provides critical insight into the role of extreme conditions in exploring unusual bonding routes that ultimately lead to the formation of novel high nitrogen content species.

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