Carbon dichalcogenides are chemical compounds of carbon and chalcogen elements. They have the general chemical formula CZ2, where Z = O, S, Se, Te.[1][2]
This includes:
- Carbon dioxide, CO2
- Carbon disulfide, CS2
- Carbon diselenide, CSe2
- Carbonyl sulfide, OCS
- Carbonyl selenide, OCSe
- Thiocarbonyl selenide, SCSe
- Thiocarbonyl telluride, SCTe[1]
Stability
editDouble bonds between carbon and chalcogen elements, C=Z, become weaker the heavier the chalcogen, Z. This trend means carbon dichalcogenide monomers are less stable and more susceptible to polymerisation as Z changes from O to Te. For example, CO2 is stable, CS2 polymerises under extreme conditions, CSe2 tends to polymerise, CSeTe is unstable and CTe2 does not exist.[1] This trend is an example of the double bond rule.
Bonding
editIn carbon dichalcogenides, C=O bond lengths are around 1.16 Å, C=S around 1.56 Å, C=Se around 1.70 Å and C=Te around 1.90 Å.[3]
Species | Formula | Z | Z′ | Bond | Bond in molecule | Bond length / Å | Method of determination | Reference |
---|---|---|---|---|---|---|---|---|
Carbon dioxide | CO2 | O | O | C=O | O=C=O | 1.163 | infrared spectroscopy | [1][3][4] |
Carbonyl sulfide | OCS | O | S | C=O | S=C=O | 1.158 | microwave spectroscopy | [5] |
Carbonyl selenide | OCSe | O | Se | C=O | Se=C=O | 1.159 | microwave spectroscopy | [3] |
Carbonyl sulfide | OCS | O | S | C=S | O=C=S | 1.560 | microwave spectroscopy | [5] |
Carbon disulfide | CS2 | S | S | C=S | S=C=S | 1.553 | infrared spectroscopy | [5] |
Thiocarbonyl selenide | SCSe | S | Se | C=S | Se=C=S | 1.553 | microwave spectroscopy | [5] |
Thiocarbonyl telluride | SCTe | S | Te | C=S | Te=C=S | 1.557 | microwave spectroscopy | [3][5][6] |
Carbonyl selenide | OCSe | O | Se | C=Se | O=C=Se | 1.709 | microwave spectroscopy | [5] |
Thiocarbonyl selenide | SCSe | S | Se | C=Se | S=C=Se | 1.693 | microwave spectroscopy | [5] |
Carbon diselenide | CSe2 | Se | Se | C=Se | Se=C=Se | 1.689 | neutron diffraction | [7] |
Thiocarbonyl telluride | SCTe | S | Te | C=Te | S=C=Te | 1.904 | microwave spectroscopy | [3][5][6] |
References
edit- ^ a b c d Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. pp. 306, 314–319, 754–755. ISBN 978-0-08-037941-8.
- ^ Housecroft, C. E.; Sharpe, A. G. (2008). Inorganic Chemistry (3rd ed.). Prentice Hall. pp. 409–412, 423–425. ISBN 978-0-13-175553-6.
- ^ a b c d e Wells, A. F. (1984). Structural Inorganic Chemistry (5th ed.). Oxford University Press. p. 926. ISBN 978-0-19-965763-6.
- ^ Plyler, Earle K.; Blaine, Lamdin R.; Tidwell, Eugene D. (1955). "Infrared absorption and emission spectra of carbon monoxide in the region from 4 to 6 microns". Journal of Research of the National Bureau of Standards. 55 (4): 183–192. doi:10.6028/jres.055.019.
- ^ a b c d e f g h William M. Haynes, ed. (2012). CRC Handbook of Chemistry and Physics (93rd ed.). CRC Press. p. 9–33. ISBN 978-1439880500.
- ^ a b Hardy, W. A.; Silvey, G. (1954). "Microwave Spectrum of TeCS and Masses of the Stable Tellurium Isotopes". Phys. Rev. 95 (2): 385–. doi:10.1103/PhysRev.95.385.
- ^ Powell, B. M.; Torrie, B. H. (1983). "Structure of solid carbon diselenide (CSe2) at 17.5, 50 and 200K". Acta Crystallogr. C. 39 (8): 3070–3072. doi:10.1107/S0108270183007015.