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Tetrakis(acetonitrile)copper(I) tetrafluoroborate

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Tetrakis(acetonitrile)copper(I) tetrafluoroborate
Identifiers
Properties
C8H12BCuF4N4
Molar mass 314.56 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Tetrakis(acetonitrile)copper(I) tetrafluoroborate is a complex compound of copper with acetonitrile as the ligand and tetrafluoroborate as the counterion.

Preparation

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Tetrakis(acetonitrile)copper(I) tetrafluoroborate can be prepared starting from nitrosyl tetrafluoroborate, which is obtained from dinitrogen tetroxide and tetrafluoroboric acid. The nitrosyl salt is then reacted with metallic copper in acetonitrile, initially producing a green-blue copper(II) complex. This complex is reduced to the copper(I) complex by further reaction with metallic copper. By boiling with additional copper powder until decolorization, the copper(I) complex is obtained.[1]

Properties

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Tetrakis(acetonitrile)copper(I) tetrafluoroborate forms colorless crystals in the orthorhombic crystal system in the space group Pna21 with the lattice parameters a = 23.882 Å; b = 8.3285 Å; c = 20.338 Å, and twelve unit cells. The compound is isomorphous with tetrakis(acetonitrile)copper(I) perchlorate and tetrakis(acetonitrile)silver(I) perchlorate.[2]

Use

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Tetrakis(acetonitrile)copper(I) tetrafluoroborate can be reacted with methoxyisobutyl isonitrile to produce Tetrakis(methoxyisobutyl isonitrile)copper(I) tetrafluoroborate.[3] This compound is used to produce technetium(99mTc)-sestamibi.[4]

See also

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References

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  1. ^ B. J. Hathaway, D. G. Holah, J. D. Postlethwaite (1961), "630. The preparation and properties of some tetrakis(methylcyanide)copper(I) complexes", Journal of the Chemical Society (Resumed), p. 3215, doi:10.1039/jr9610003215{{citation}}: CS1 maint: multiple names: authors list (link)
  2. ^ P. G. Jones, O. Crespo (1998-01-15), "Tetrakis(acetonitrile- N )copper(I) Tetrafluoroborate", Acta Crystallographica Section C Crystal Structure Communications, vol. 54, no. 1, pp. 18–20, doi:10.1107/S0108270197013322
  3. ^ Te-Wei Lee, Chang-Shinn Su, Gann Ting (February 1996), "Synthesis, reactivity and 99mTc labelling of 2-alkoxyisobutylisonitrile", Applied Radiation and Isotopes, vol. 47, no. 2, pp. 207–210, doi:10.1016/0969-8043(95)00249-9{{citation}}: CS1 maint: multiple names: authors list (link)
  4. ^ M. E. Wilson, J. C. Hung, R. J. Gibbons (July 1993), "An alternative method for rapid preparation of 99Tcm-sestamibi:", Nuclear Medicine Communications, vol. 14, no. 1, pp. 544–549, doi:10.1097/00006231-199307000-00005{{citation}}: CS1 maint: multiple names: authors list (link)