4.8 Article

Molecular Ruby under Pressure

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 57, Issue 34, Pages 11069-11073

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201806755

Keywords

chromium; excited states; luminescence; pressure; spin-flip

Funding

  1. Deutsche Forschungsgemeinschaft [GSC 266, HE 2778/10-1]
  2. internal university research funds of the Johannes Gutenberg University, Mainz (Germany)
  3. Natural Sciences and Engineering Research Council of Canada
  4. DAAD

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The intensely luminescent chromium(III) complexes [Cr(ddpd)(2)](3+) and [Cr(H(2)tpda)(2)](3+) show surprising pressure-induced red shifts of up to -15cm(-1) kbar(-1) for their sharp spin-flip emission bands (ddpd=N,N-dimethyl-N,N-dipyridine-2-yl-pyridine-2,6-diamine; H(2)tpda=2,6-bis(2-pyridylamino)pyridine). These shifts surpass that of the established standard, ruby Al2O3:Cr3+, by a factor of 20. Beyond the common application in the crystalline state, the very high quantum yield of [Cr(ddpd)(2)](3+) enables optical pressure sensing in aqueous and methanolic solution. These unique features of the molecular rubies [Cr(ddpd)(2)](3+) and [Cr(H(2)tpda)(2)](3+) pave the way for highly sensitive optical pressure determination and unprecedented molecule-based pressure sensing with a single type of emitter.

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