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Isoselenocarbonyl complexes.

Ian A Cade1, Anthony F Hill, Caitlin M A McQueen

  • 1Research School of Chemistry, The Australian National University, Canberra, ACT 2601, Australia. a.hill@anu.edu.au.

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|January 19, 2019
PubMed
Summary
This summary is machine-generated.

Salt elimination reactions involving a molybdenum isoselenocarbonyl complex successfully synthesized novel molybdenum-ruthenium and molybdenum-iron derivatives. These new complexes expand the scope of isoselenocarbonyl chemistry.

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Area of Science:

  • Organometallic Chemistry
  • Coordination Chemistry
  • Main Group Chemistry

Background:

  • The synthesis of metal-containing heterocumulenes is a developing area.
  • Isoselenocarbonyl complexes are of interest due to their unique bonding and reactivity.

Purpose of the Study:

  • To investigate the salt elimination reactions of [NEt4][Mo(CSe)(CO)2(Tp*)] with metal halide complexes.
  • To synthesize and characterize novel isoselenocarbonyl complexes.

Main Methods:

  • Salt elimination reactions.
  • Reactions with metal halide complexes including ruthenium and iron.
  • Structural characterization using X-ray crystallography.
  • Spectroscopic and microanalytical data analysis.

Main Results:

  • Synthesis of molybdenum-ruthenium derivatives [Mo{CSeRu(L)2(η-C5R5)}(CO)2(Tp*)] (L = PPh3, R = H 4; L = CO, R = Me 5).
  • Synthesis of molybdenum-iron derivative [Mo{CSeFe(CO)2(η-C5H5)}(CO)2(Tp*)] (6).
  • Structural characterization of two molybdenum-ruthenium derivatives and one hydrido-isoselenocarbonyl complex [Mo{CSeRuH(CO)2(PPh3)2}(CO)2(Tp*)] (7).

Conclusions:

  • Salt elimination reactions provide a viable route to novel isoselenocarbonyl complexes.
  • The synthesized complexes demonstrate the versatility of the [Mo(CSe)(CO)2(Tp*)] precursor.
  • Further investigation into the reactivity of these complexes is warranted.