Skip to main content
Log in

Trialkyl Triphenyl Phosphonium Dicyanodibromoaurates [Ph3PAlk][Au(CN)2Br2], Alk = CH2C6H4(OH)-2, CH2C6H11-cyclo, CH2Ph, CH2C6H4CN-4

  • COORDINATION COMPOUNDS
  • Published:
Russian Journal of Inorganic Chemistry Aims and scope Submit manuscript

Abstract

The crystalline yellow complexes [Ph3PAlk][Au(CN)2Br2], where Alk = CH2C6H4(OH)-2 (I), CH2C6H11-cyclo (II ⋅ 1/2PhH), CH2Ph (III), CH2C6H4CN-4 (IV), have been synthesized from potassium dicyanodibromoaurate and alkyl triphenyl phosphonium chlorides in water and structurally characterized by X-ray diffraction. Crystals of complexes IIV contain tetrahedral alkyl triphenyl phosphonium cations (CPC, 104.8(2)°–114.1(2)°; P–C, 1.782(6)–1.825(5) Å). In square [Au(CN)2Br2] anions, the CAuC and BrAuBr trans-angles are 178.8(2)°–180.0(5)° and 178.38(3)°–180.00(3)°, and the Au–C and Au–Br bonds are 2.001(7)–2.205(9) Å and 2.4086(14)–2.4276(18) Å, respectively. The crystal structures are formed by weak hydrogen bonds N⋅⋅⋅Н–С and strong bonds N⋅⋅⋅Н–О in complex I and contacts Br⋅⋅⋅Н–С in dicyano-dibromides I, III, and IV.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1.
Fig. 2.
Fig. 3.
Fig. 4.
Fig. 5.

Similar content being viewed by others

REFERENCES

  1. L. Xiaobo and H. Patterson, Materials 6, 2595 (2013). https://doi.org/10.3390/ma6072595

    Article  CAS  Google Scholar 

  2. P. Dechambenoit, S. Ferlay, N. Kyritsakas, et al., Cryst. Eng. Commun. 13, 1922 (2011). https://doi.org/10.1039/C0CE00607F

    Article  CAS  Google Scholar 

  3. J. A. Hill, A. L. Thompson, and A. L. Goodwin, J. Am. Chem. Soc. 138, 5886 (2018). https://doi.org/10.1021/jacs.5b13446

    Article  CAS  Google Scholar 

  4. Z. Assefa, R. G. Haire, and R. E. Sykora, J. Solid State Chem. 181, 382 (2008). https://doi.org/10.1016/j.jssc.2007.11.036

    Article  CAS  Google Scholar 

  5. M. L. Brown, J. S. Ovens, and D. B. Leznoff, Dalton Trans. 46, 7169 (2017). https://doi.org/10.1039/C7DT00942A

    Article  CAS  PubMed  Google Scholar 

  6. S. Chorazy, M. Wyczesany, and B. Sieklucka, Molecules 22, 1902 (2017). https://doi.org/10.3390/molecules22111902

    Article  CAS  PubMed Central  Google Scholar 

  7. C. F. Shaw, Chem. Rev. 99, 2589 (1999). https://doi.org/10.1021/cr980431o

    Article  CAS  Google Scholar 

  8. M. A. Rawashdeh-Omary, M. A. Omary, and H. H. Patterson, J. Am. Chem. Soc. 122, 10371 (2000). https://doi.org/10.1021/ja001545w

    Article  CAS  Google Scholar 

  9. M. A. Rawashdeh-Omary, M. A. Omary, G. E. Shankle, et al., J. Phys. Chem. B 104, 6143 (2000). https://doi.org/10.1021/jp000563x

    Article  CAS  Google Scholar 

  10. J. C. F. Colis, C. Larochelle, E. J. Fernández, et al., J. Phys. Chem. B 109, 4317 (2005). https://doi.org/10.1021/jp045868g

    Article  CAS  PubMed  Google Scholar 

  11. Z. Assefa, K. Kalachnikova, R. G. Haire, et al., J. Solid State Chem. 180, 3121 (2007). https://doi.org/10.1016/j.jssc.2007.08.032

    Article  CAS  Google Scholar 

  12. R. J. Roberts, D. Le, and D. B. Leznoff, Inorg. Chem. 56, 7948 (2017). https://doi.org/10.1021/acs.inorgchem.7b00735

    Article  CAS  PubMed  Google Scholar 

  13. J. S. Ovens and D. B. Leznoff, Dalton Trans. 40, 4140 (2011). https://doi.org/10.1039/c0dt01772h

    Article  CAS  PubMed  Google Scholar 

  14. J. S. Ovens, K. N. Truong, and D. B. Leznof, Dalton Trans. 41, 1345 (2012). https://doi.org/10.1039/c1dt11741f

    Article  CAS  PubMed  Google Scholar 

  15. J. S. Ovens and D. B. Leznoff, Chem. Mater. 27, 1465 (2015). https://doi.org/10.1021/cm502998w

    Article  CAS  Google Scholar 

  16. Cambridge Crystallographic Data Center. 2018. deposit@ccdc.cam.ac.uk; http://www.ccdc.cam.ac.uk.

  17. V. V. Sharutin, M. A. Popkova, and N. M. Tarasova, Bull. South Ural State Univ., Ser. Chem. 10 (1), 55 (2018). https://doi.org/10.14529/chem180107

    Article  Google Scholar 

  18. J. S. Ovens, A. R. Geisheimer, A. A. Bokov, et al., Inorg. Chem. 49, 9609 (2010). https://doi.org/10.1021/ic101357y

    Article  CAS  PubMed  Google Scholar 

  19. B. Pitteri, M. Bortoluzzi, and V. Bertolasi, Trans. Met. Chem. 33, 649 (2008). https://doi.org/10.1007/s11243-008-9092-9

    Article  CAS  Google Scholar 

  20. G. Marangoni, B. Pitteri, V. Bertolasi, et al., J. Chem. Soc., Dalton Trans., No. 1, 2235 (1987). https://doi.org/10.1039/DT9870002235

  21. J. S. Ovens, K. N. Truong, and D. B. Leznoff, Inorg. Chim. Acta 403, 127 (2013). https://doi.org/10.1016/j.ica.2013.02.011

    Article  CAS  Google Scholar 

  22. SMART and SAINT-Plus: Data Collection and Processing Software for the SMART System, Versions 5.0 (Bruker, Madison, Wisconsin, 1998).

  23. SHELXTL/PC: An Integrated System for Solving, Refining and Displaying Crystal Structures from Diffraction Data, Versions 5.10 (Bruker, Madison, Wisconsin, 1998).

  24. O. V. Dolomanov, L. J. Bourhis, R. J. Gildea, et al., J. Appl. Crystallogr. 42, 339 (2009). https://doi.org/10.1107/S0021889808042726

    Article  CAS  Google Scholar 

  25. E. Pretsch, P. Buhlmann, and C. Affolter, Structure Determination of Organic Compounds. Tables of Spectral Data (Springer, 2000; Mir, Moscow, 2006).

  26. L. Jones, Inorg. Chem. 3, 1581 (1964). https://doi.org/10.1021/ic50021a024

    Article  CAS  Google Scholar 

  27. C. J. Shorrock, H. Jong, R. J. Batchelor, et al., Inorg. Chem. 42, 3917 (2003). https://doi.org/10.1021/ic034144

    Article  CAS  PubMed  Google Scholar 

  28. B. Cordero, V. Gómez, A. E. Platero-Prats, et al., Dalton Trans., 2832 (2008). https://doi.org/10.1039/b801115j

  29. M. Mantina, A. C. Chamberlin, R. Valero, et al., J. Phys. Chem. A 113, 5806 (2009). https://doi.org/10.1021/jp8111556

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Funding

The National South Ural State Research University is grateful to the Ministry of Science and Higher Education of the Russian Federation for financial support (grant no. 4.6151.2017/8.9).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to N. M. Tarasova.

Ethics declarations

The authors declare that they have no conflict of interest.

Additional information

Translated by E. Glushachenkova

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sharutin, V.V., Sharutina, O.K., Tarasova, N.M. et al. Trialkyl Triphenyl Phosphonium Dicyanodibromoaurates [Ph3PAlk][Au(CN)2Br2], Alk = CH2C6H4(OH)-2, CH2C6H11-cyclo, CH2Ph, CH2C6H4CN-4. Russ. J. Inorg. Chem. 65, 169–175 (2020). https://doi.org/10.1134/S0036023620020151

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S0036023620020151

Keywords:

Navigation