- Organoantimony chemistry
Organoantimony chemistry is the chemistry of compounds containing a carbon to antimony (Sb) chemical bond. Relevant oxidation states are Sb(V) and Sb(III). The toxicity of antimony limits practical application in organic chemistry.
Antimony compounds of the type R5Sb (stiboranes) can be synthesised from trivalent Sb precursors:
- Ph3Sb + Cl2 → Ph3SbCl2
- Ph3SbCl2 + 2 PhLi → Ph5Sb
Asymmetric compounds can also be obtained through the stibonium ion:
- R5Sb + X2 → [R4Sb]+[X]
- [R4Sb]+[X] + R'MgX → R4R'Sb
Just as in the related organobismuth compounds (same group 15), organoantimony(V) compounds form onium compounds and ate complexes.
Pentaphenylantimony decomposes at 200 °C to triphenylstibine and biphenyl. It forms a trigonal bipyramidal molecular geometry. In the related Me5Sb all methyl protons are equivalent at -100 °C in proton NMR. Compounds of the type R4SbX tend to form dimers.
- SbCl3 + 3 RLi (or RMgCl) → R3Sb
Typical reactions are:
- R3Sb + Br2 → R3SbBr2
- R3Sb + O2 → R3SbO
- R3Sb + Na + NH3 → R2SbNa
- R3Sb + B2H6 → R3Sb.BH3
Stibanes are weak Lewis acids and therefore ate complexes are not encountered. On the other hand they have good donor properties and are therefore widely used in coordination chemistry. R3Sb compounds are more air-sensitive than the R5Sb counterparts.
Antimony Metallocenes are known as well:
- 14SbI3 + 3 (Cp*Al)4 → [2Cp*Sb]+[AlI4]- + 8Sb + 6 AlI3
The Cp*-Sb-Cp* angle is 154°.
Distibines have a Sb-Sb single bond and are of some interest as thermochromic materials. For example tetramethyldistibine is a colorless as a gas, yellow as a liquid, red as solid just below the melting point of 18.5 °C and again yellow well below the melting point. 
- Chemical bonds of carbon with other elements in the periodic table:
CH He CLi CBe CB CC CN CO CF Ne CNa CMg CAl CSi CP CS CCl CAr CK CCa CSc CTi CV CCr CMn CFe CCo CNi CCu CZn CGa CGe CAs CSe CBr CKr CRb CSr CY CZr CNb CMo CTc CRu CRh CPd CAg CCd CIn CSn CSb CTe CI CXe CCs CBa CHf CTa CW CRe COs CIr CPt CAu CHg CTl CPb CBi CPo CAt Rn Fr Ra Rf Db Sg Bh Hs Mt Ds Rg Cn Uut Uuq Uup Uuh Uus Uuo ↓ CLa CCe CPr CNd CPm CSm CEu CGd CTb CDy CHo CEr CTm CYb CLu Ac Th Pa CU Np Pu Am Cm Bk Cf Es Fm Md No Lr Chemical bonds to carbon Core organic chemistry Many uses in chemistry Academic research, but no widespread use Bond unknown / not assessed
- ^ Filella, M.. "Alkyl derivatives of antimony in the environment". Metal ions in life sciences (Cambridge: RSC publishing) 7: 267–301. ISBN 9781847551771..
- ^ C. Elschenbroich, A. Salzer Organometallics : A Concise Introduction (2nd Ed) (1992) from Wiley-VCH: Weinheim. ISBN 3-527-28165-7
- ^ Organoantimony compounds with element-element bonds H.J. Breunig, R. Rosler Coordination Chemistry Reviews 163 (1997) 33-53
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Look at other dictionaries:
Antimony — This article is about the element. For the town, see Antimony, Utah. Not to be confused with Antinomy, a type of paradox. tin ← antimony → tellurium As ↑ Sb ↓ Bi … Wikipedia
Triphenylstibine — Chembox new Name = Triphenylstibine ImageFile = Triphenylphosphine 3D sticks.png ImageName = 3D structure of PPh3 IUPACName = Triphenylstibine OtherNames = Triphenylantimony Section1 = Chembox Identifiers CASNo = 603 36 1 RTECS = WJ1400000… … Wikipedia