Triethyl­ammonium tetra­chlorido(pyridine-2-carboxyl­ato-κ2N,O)stannate(IV)
2011

Triethylammonium Tetra­chlorido(pyridine-2-carboxyl­ato)stannate(IV)

publication

Author Information

Author(s): Najafi Ezzatollah, Amini Mostafa M., Ng Seik Weng

Primary Institution: Shahid Beheshti University, Tehran, Iran

Hypothesis

The study investigates the synthesis of a new metal-organic compound using triethylamine as a proton abstractor.

Conclusion

The reaction successfully produced a new salt with a stannate anion chelated by a pyridine-2-carboxylate group.

Supporting Evidence

  • The cation and the anion in the title salt are linked by an N—H⋯O hydrogen bond.
  • The SnIV atom in the stannate anion is chelated by the pyridine-2-carboxyl­ate group.
  • The cation is disordered over two positions in a 0.564(1):0.436(1) ratio.

Takeaway

The researchers made a new chemical compound by mixing some ingredients together, and it turned out well!

Methodology

The reaction was carried out under nitrogen atmosphere with specific amounts of pyridine-2-carboxylic acid, triethylamine, and stannic chloride in dry methanol.

Digital Object Identifier (DOI)

10.1107/S1600536811005460

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