Crystals of the title salt, (C8H20N)[Sn(C6H5)3(C2H2O2S)], comprise diisobutylammonium cations and mercaptoacetatotriphenylstannate(IV) anions. The bidentate binding mode of the mercaptoacetate ligand gives rise to a five-coordinated, ionic triphenyltin complex with a distortedcis-trigonal–bipyramidal geometry around the tin atom. In the crystal, charge-assisted ammonium-N—H...O(carboxylate) hydrogen-bonding connects two cations and two anions into a four-ion aggregate. Two positions were resolved for one of the phenyl rings with the major component having a site occupancy factor of 0.60 (3).
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Crystal structures of sodium-, lithium-, and ammonium 4,5-dihydroxybenzene-1,3-disulfonate (tiron) hydrates
The solid-state structures of the Na + , Li + , and NH 4 + salts of the 4,5-dihydroxybenzene-1,3-disulfonate (tiron) dianion are reported, namely disodium 4,5-dihydroxybenzene-1,3-disulfonate, 2Na + ·C 6 H 4 O 8 S 2 2− , μ-4,5-dihydroxybenzene-1,3-disulfonato-bis[aqualithium(I)] hemihydrate, [Li 2 (C 6 H 4 O 8 S 2 )(H 2 O) 2 ]·0.5H 2 O, and diammonium 4,5-dihydroxybenzene-1,3-disulfonate monohydrate, 2NH 4 + ·C 6 H 4 O 8 S 2 2− ·H 2 O. Intermolecular interactions vary with the size of the cation, and the asymmetric unit cell, and the macromolecular features are also affected. The sodium in Na 2 (tiron) is coordinated in a distorted octahedral environment through the sulfonate oxygen and hydroxyl oxygen donors on tiron, as well as an interstitial water molecule. Lithium, with its smaller ionic radius, is coordinated in a distorted tetrahedral environment by sulfonic and phenolic O atoms, as well as water in Li 2 (tiron). The surrounding tiron anions coordinating to sodium or lithium in Na 2 (tiron) and Li 2 (tiron), respectively, result in a three-dimensional network held together by the coordinate bonds to the alkali metal cations. The formation of such a three-dimensional network for tiron salts is relatively rare and has not been observed with monovalent cations. Finally, (NH 4 ) 2 (tiron) exhibits extensive hydrogen-bonding arrays between NH 4 + and the surrounding tiron anions and interstitial water molecules. This series of structures may be valuable for understanding charge transfer in a putative solid-state fuel cell utilizing tiron.
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- Award ID(s):
- 1708793
- PAR ID:
- 10073869
- Date Published:
- Journal Name:
- Acta Crystallographica Section E Crystallographic Communications
- Volume:
- 74
- Issue:
- 7
- ISSN:
- 2056-9890
- Page Range / eLocation ID:
- 918 to 925
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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