Chemistry:Transition metal sulfate complex

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Short description: Coordination complexes with one or more sulfate ligands
Some bonding modes in sulfate complexes.

Transition metal sulfate complexes or sulfato complexes are coordination complexes with one or more sulfate ligands. Sulfate binds to metals through one, two, three, or all four oxygen atoms.[1] Common are complexes where sulfate is unidentate or chelating bidentate. Examples are respectively [Co(tren)(NH3)(SO4)]+ (tren = tris(2-aminoethyl)amine)[2] and Co(phen)2SO4.[3] All four oxygen atoms of sulfate bond to metals in some Dawson-type polyoxometalates, e.g. [S2Mo18O62]4-.[4]

Sulfate as a counterion

Being the conjugate base of a strong acid (sulfuric acid), sulfate is not basic. It is more commonly a counterion in coordination chemistry. Tutton's salts, with the formula M'2M(SO4)2(H2O)6 (M' = K+, etc.; M = Fe2+, etc.), illustrate the ability of water to outcompete sulfate as a ligand for M2+. Similarly alums, such as chrome alum ([K(H2O)6][Cr(H2O)6][SO4]2), features [Cr(H
2O)
6]3+ with noncoordinated sulfate. In a related vein, some sulfato complexes confirmed by X-ray crystallography, convert to simple aquo complexes when dissolved in water. Copper(II) sulfate examplifies this behavior, sulfate is bonded to copper in the crystal but dissociates upon dissolution.

Synthesis

Structure of [Pt(NH3)4(NO)(SO4)]+. Selected bond distances: Pt-O, 2.284; S-O range from 1.496 to 1.462 Å. [5] Color code: blue = N, red = O, dark blue = Pt.

Sulfato complexes are commonly produced by reaction of metal sulfates with other ligands.

In some cases, sulfato complexes are produced from sulfur dioxide:[6]

Pt(O
2)(PPh
3)
2 + SO
2 → Pt(SO
4)(PPh
3)
2 (PPh3 = triphenylphosphine)

Sulfato complexes also arise by air-oxidation of metal sulfides.[7]

Reactions

Sulfato complexes are susceptible to protonation of uncoordinated oxygen atoms.[8]

References

  1. ↑ Papatriantafyllopoulou, Constantina; Aromi, Guillem; Tasiopoulos, Anastasios J.; Nastopoulos, Vassilios; Raptopoulou, Catherine P.; Teat, Simon J.; Escuer, Albert; Perlepes, Spyros P. (2007). "Use of the Sulfato Ligand in 3d‐Metal Cluster Chemistry: A Family of Hexanuclear Nickel(II) Complexes with 2‐Pyridyl‐Substituted Oxime Ligands". European Journal of Inorganic Chemistry 2007 (18): 2761–2774. doi:10.1002/ejic.200700063. 
  2. ↑ Chun, Hyungphil; Jackson, W. Gregory; McKeon, Josephine A.; Somoza, Fernando B.; Bernal, Ivan (2000). "The Interaction between Amminehalocobalt(III) Cations and Polythionate Anions: Hydrogen-Bonding Patterns and S–S Bond Cleavage Reactions". European Journal of Inorganic Chemistry 2000: 189–193. doi:10.1002/(SICI)1099-0682(200001)2000:1<189::AID-EJIC189>3.0.CO;2-V. 
  3. ↑ Zhong, Kai-Long (2013). "Bis(1,10-phenanthroline-κ2 N , N ′)(sulfato-κ2 O , O ′)cobalt(II) propane-1,2-diol monosolvate". Acta Crystallographica Section E 69 (Pt 1): m26. doi:10.1107/S1600536812049616. PMID 23476325. 
  4. ↑ Juraja, Suzy; Vu, Truc; Richardt, Peter J. S.; Bond, Alan M.; Cardwell, Terence J.; Cashion, John D.; Fallon, Gary D.; Lazarev, Georgii et al. (2002). "Electrochemical, Spectroscopic, Structural, and Magnetic Characterization of the Reduced and Protonated α-Dawson Anions in [Fe(η5-C5Me5)2]5[HS2Mo18O62]·3HCONMe2·2Et2O and [NBu4]5[HS2Mo18O62]·2H2O1". Inorganic Chemistry 41 (5): 1072–1078. doi:10.1021/ic010780s. PMID 11874340. 
  5. ↑ Schaniel, Dominik; Woike, Theo; Behrnd, Norwid-R.; Hauser, Jürg; Krämer, Karl W.; Todorova, Teodora; Delley, Bernard (2009). "Photogeneration of Nitrosyl Linkage Isomers in Octahedrally Coordinated Platinum Complexes in the Red Spectral Range". Inorganic Chemistry 48 (23): 11399–11406. doi:10.1021/ic901392q. PMID 19863116. 
  6. ↑ Cook, Christopher David.; Jauhal, G. S. (1967). "Oxidation of Coordinated Ligands. Sulfato and Nitrato Complexes of Platinum". Journal of the American Chemical Society 89 (12): 3066–3067. doi:10.1021/ja00988a057. 
  7. ↑ Kim, Chang G.; Coucouvanis, Dimitri (1993). "Dimerization of the molybdenum complex[(SO4)Mo(O)(mu-S)2Mo(O)(SO4)]2- Dianions Stabilized by a Quadruply Bridging Sulfate Ligand and Intramolecular Hydrogen Bonding by the [(CH3)2NH2]+ Cations. Structures of the [(CH3)2NH2]6-x(Et4N)x[(SO4)Mo(O)(mu-S)2Mo(O)(SO4)]2(SO4)] Aggregates (x = 1, 2, 2.5)". Inorganic Chemistry 32 (11): 2232–2233. doi:10.1021/ic00063a004. 
  8. ↑ Scheidt, W. Robert; Lee, Young Ja; Finnegan, Michael G. (1988). "Reactions of Sulfur Dioxide with Iron Porphyrinates and the Crystal Structure of (Hydrogen sulfato)(tetraphenylporphinato)iron(III) Hemibenzene Solvate". Inorganic Chemistry 27 (26): 4725–4730. doi:10.1021/ic00299a010. 



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