addenda and errata\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

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ISSN: 2056-9890

Poly[μ2-chlorido-nona­methyl-μ3-nitrato-tritin(IV)]. Corrigendum

aDepartment of Chemistry, University of Azad Jammu and Kashmir, Muzaffarabad, Pakistan, bDepartment of Chemistry, Quaid-i-Azam University, Islamabad 45320, Pakistan, cDepartment of Chemistry, G.C. University, Faisalabad, Pakistan, and dSchool of Chemistry, The University of Manchester, Manchester M13 9PL, England
*Correspondence e-mail: drsa54@yahoo.com

(Received 4 June 2008; accepted 6 June 2008; online 21 June 2008)

An error in the original formulation of the title compound in the paper by Sadiq-ur-Rehman, Sherzaman, Ali, Shahzadi & Helliwell [Acta Cryst. (2007), E63, m2329 ] is corrected.The title compound in the paper by Sadiq-ur-Rehman, Sherzaman, Ali, Shahzadi & Helliwell [Acta Cryst. (2007), E63, m2329 ] was an unexpected product which seemed to have nitrate coordinated to three Sn atoms. However, it was noticed that the charges do not balance and that it is most likely that the nitrate is in fact a carbonate. Regrettably, there is no material to carry out microanalysis, but a plausible mechanism has been suggested to explain the unexpected formation of the product. Trimethyl­tin chloride will react with methanol in the presence of a base (4-hydroxy­piperidine) to give trimethyl­tin methoxide, which will rapidly hydrolyze in air to give the hydroxide. Both the methoxide and the hydroxide will react with atmospheric CO2 to give the carbonate (Bloodworth et al., 1967[Bloodworth, A. J., Davies, A. G. & Vasishtha, S. V. (1967). J. Chem. Soc. C, pp. 1309-1313.]; Blunden et al., 1984[Blunden, S. J., Hill, R. & Ruddick, J. N. R. (1984). J. Organomet. Chem. 267, C5.]; Sato, 1967[Sato, H. (1967). Bull. Chem. Soc. Jpn, 40, 410-411.]). Me3SnCl + MeOH + base → Me3SnOMe + base·HCl Me3SnOMe + H2O → Me3SnOH + MeOH Me3SnOH + CO2 → Me3SnOCO2HMe3SnOCO2H + Me3SnOMe → Me3SnOCO2SnMe3 + MeOH. The carbonate then forms a coordination copolymer with trimethyl­tin chloride. The name of the title compound is corrected to poly[μ3-carbonato-μ3-chlorido-nona­methyl­tri­tin(IV)], [Sn3(CH3)9(CO3)Cl] (Mr = 586.84).

[Scheme 1]

Acknowledgements

We thank Professor Alwyn G. Davies (Department of Chemistry, University College London, UK) for providing the mechanism to explain the unexpected formation of the product.

References

First citationBloodworth, A. J., Davies, A. G. & Vasishtha, S. V. (1967). J. Chem. Soc. C, pp. 1309–1313.  Google Scholar
First citationBlunden, S. J., Hill, R. & Ruddick, J. N. R. (1984). J. Organomet. Chem. 267, C5.  CrossRef Web of Science Google Scholar
First citationSato, H. (1967). Bull. Chem. Soc. Jpn, 40, 410–411.  CrossRef CAS Web of Science Google Scholar

This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

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ISSN: 2056-9890
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