Английская Википедия:Iron tris(dimethyldithiocarbamate)

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Шаблон:Chembox

Iron tris(dimethyldithiocarbamate) is the coordination complex of iron with dimethyldithiocarbamate with the formula Fe(S2CNMe2)3 (Me = methyl). It is marketed as a fungicide.[1]

Synthesis, structure, bonding

Iron tris(dithiocarbamate)s are typically are prepared by salt metathesis reactions.[1]

Iron tris(dimethyldithiocarbamate) is an octahedral coordination complex of iron(III) with D3 symmetry.[2]

Spin crossover (SCO) was first observed in 1931 by Cambi et al. who discovered anomalous magnetic behavior for the tris(N,N-dialkyldithiocarbamatoiron(III) complexes.[3] The spin states of these complexes are sensitive to the nature of the amine substituents.[4]

Reactions

Iron tris(dithiocarbamate)s react with nitric oxide to give a nitrosyl complex:

Шаблон:Chem2

This efficient chemical trapping reaction provides a means to detect NO.[5]

Reflecting the strongly donating properties of dithiocarbamate ligands, iron tris(dithiocarbamate)s oxidize at relatively mild potentials to give isolable iron(IV) derivatives [Fe(S2CNR2)3]+.[6]

Iron tris(dithiocarbamate)s react with hydrochloric acid to give the pentacoordinate chloride:[7]

Шаблон:Chem2

Safety

The U.S. Occupational Safety and Health Administration (OSHA) has set the legal (permissible exposure limit) for ferbam exposure in the workplace as 15 mg/m3 over an 8-hour workday. The U.S. National Institute for Occupational Safety and Health (NIOSH) has set a recommended exposure limit (REL) of 1 mg/m3 over an 8-hour workday. At levels of 800 mg/m3, ferbam is immediately dangerous to life and health.[8]

See also

References

Шаблон:Reflist

  1. 1,0 1,1 Шаблон:Cite journal
  2. Шаблон:Cite journal
  3. Шаблон:Cite journal
  4. Шаблон:Cite book
  5. Шаблон:Cite journal
  6. Шаблон:Cite journal
  7. Шаблон:Cite journal
  8. Ошибка цитирования Неверный тег <ref>; для сносок PGCH не указан текст