The compound (C5H5)2TiS5 is an example of a polysulfide complex
Polysulfides are a class of chemical compounds derived from anionic chains of sulfur atoms.[1] There are two main classes of polysulfides: inorganic and organic. The inorganic polysulfides have the general formula S2− n. These anions are the conjugate bases of polysulfanesH2Sn. Organic polysulfides generally have the formulae R1SnR2, where R is an alkyl or aryl group.[2]
Polysulfide salts and complexes
Fragment of the solid-state structure of Na2S5. The S2−5 chain consists of the yellow-colored atoms.[3]
In some cases, these anions have been obtained as organic salts, which are soluble in organic solvents.[4]
The energy released in the reaction of sodium and elemental sulfur is the basis of battery technology. The sodium–sulfur battery and the lithium–sulfur battery require high temperatures to maintain liquid polysulfide and Na+-conductive membranes that are unreactive toward sodium, sulfur, and sodium sulfide.
Polysulfides are ligands in coordination chemistry. Examples of transition metal polysulfido complexes include (C5H5)2TiS5, [Ni(S4)2]2−, and [Pt(S5)3]2−.[5] Main group elements also form polysulfides.[6]
In commerce, the term "polysulfide" usually refers to a class of polymers with alternating chains of several sulfur atoms and hydrocarbons. They have the formula R1SnR2. In this formula n indicates the number of sulfur atoms (or "rank"). Polysulfide polymers can be synthesized by condensation polymerization reactions between organic dihalides and alkali metal salts of polysulfide anions:
n Na2S5 + n ClCH2CH2Cl → [CH2CH2S5]n + 2n NaCl
Dihalides used in this condensation polymerization are dichloroalkanes such as 1,2-dichloroethane, bis(2-chloroethoxy)methane (ClCH2CH2OCH2OCH2CH2Cl), and 1,3-dichloropropane. The polymers are called thiokols. In some cases, polysulfide polymers can be formed by ring-opening polymerization reactions.
Polysulfide polymers are also prepared by the addition of polysulfanes to alkenes. An idealized equation is:
2 RCH=CH2 + H2Sn → (RCH2CH2)2Sn
In reality, homogeneous samples of H2Sn are difficult to prepare.[2]
Polysulfide polymers are insoluble in water, oils, and many other organic solvents. Because of their solvent resistance, these materials find use as sealants to fill the joints in pavement, automotive window glass, and aircraft structures.
Polymers containing one or two sulfur atoms separated by hydrocarbon sequences are usually not classified polysulfides, e.g. poly(p-phenylene) sulfide(C6H4S)n.
Polysulfides in vulcanized rubber
Idealized structure of two strands (blue and green) of natural rubber after vulcanization with elemental sulfur, which forms polysulfide linkages.
Many commercial elastomers contain polysulfides as crosslinks. These crosslinks interconnect neighboring polymer chains, thereby conferring rigidity. The degree of rigidity is related to the number of crosslinks. Elastomers, therefore, have a characteristic ability to return to their original shape after being stretched or compressed. Because of this memory for their original cured shape, elastomers are commonly referred to as rubbers. The process of crosslinking the polymer chains in these polymers with sulfur is called vulcanization. The sulfur chains attach themselves to the allylic carbon atoms, which are adjacent to C=C linkages. Vulcanization is a step in the processing of several classes of rubbers, including polychloroprene (Neoprene), styrene-butadiene, and polyisoprene, which is chemically similar to natural rubber. Charles Goodyear's discovery of vulcanization, involving the heating of polyisoprene with sulfur, was revolutionary because it converted a sticky and almost useless material into an elastomer that could be fabricated into useful products.
Occurrence in gas giants
In addition to water and ammonia, the clouds in the atmospheres of the gas giant planets contain ammonium sulfides. The reddish-brownish clouds are attributed to polysulfides, arising from the exposure of the ammonium sulfides to light.[7]
^Dev, S.; Ramli, E.; Rauchfuss, T. B.; Wilson, S. R. (1991). "Synthesis and Structure of [M(N-Methylimidazole)6]S8: Polysulfide Salts Prepared by the Reaction N-Methylimidazole + Metal Powder + Sulfur". Inorg. Chem.30 (11): 2514. doi:10.1021/ic00011a011.
^Draganjac, M. E.; Rauchfuss, T. B. (1985). "Transition Metal Polysulfides: Coordination Compounds with Purely Inorganic Chelate Ligands". Angew. Chem. Int. Ed. Engl. 24 (9): 742. doi:10.1002/anie.198507421.
^Takeda, N.; Tokitoh, N.; Okazaki, R. (2003). Polysulfido Complexes of Main Group and Transition Metals. Topics in Current Chemistry. Vol. 231. pp. 153–202. doi:10.1007/b13184. ISBN3-540-40378-7.
