Disilene

Disilene
Names
IUPAC name
Disilene
Identifiers
CAS Number
  • 15435-77-5 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 123409 checkY
PubChem CID
  • 139934
CompTox Dashboard (EPA)
  • DTXSID50165597 Edit this at Wikidata
InChI
  • InChI=1S/H4Si2/c1-2/h1-2H2
    Key: IKQCSDAPCHQIFR-UHFFFAOYSA-N
  • [SiH2]=[SiH2]
Properties
Chemical formula
H4Si2
Molar mass 60.202 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Disilene is an inorganic compound with the chemical formula Si
2
H
4
. The name disilene, referring to the structure of a particular prototropic tautomer of the molecule. It is the simplest silene.

Properties and bonding

Disilene is a molecule with one Si=Si bond and four equivalent Si-H bonds. Its structure is like that of ethylene if ethylene's carbon atoms were replaced by silicon. However, unlike ethylene, disilene is kinetically unstable with respect to tautomerisation. Disilene has two other tautomers, that are very close in energy: (μ2-H)disilene, and disilanylidene.[1]

Organodisilenes

Structure of tetramesityl disilene.

Disilenes bearing sterically bulky substituents are isolable and have been well characterized although they remain mainly of academic interest. The first stabilised disilene was tetramesityldisilene, (C6Me3H2)4Si2. The Si=Si distance in this molecule is 2.15 Å, about 10% shorter than a typical Si–Si single bond. The Si2C4 core is roughly planar.[2] Such species are typically prepared by reduction of organosilicon halides:

2 R2SiCl2 + 4 Na → R2Si=SiR2 + 4 NaCl.

An alternative synthesis involves photolysis of trisilacyclopropanes. When the R group is not bulky, cyclic or polymeric, polysilanes are the products.

In one study[3] a disilene is prepared by an intramolecular coupling of a 1,1-dibromosilane with potassium graphite. The silicon double bond in the resulting compound has a bond length of 227 picometer (second largest ever found) with trans-bent angles 33° and 31° (by X-ray diffraction).

Tricyclic disilenes with highly strained Si-Si double bonds

In addition to this the substituents around the Si-Si bond are twisted by 43°. The disilene isomerizes to a tetracyclic compound by heating at 110 °C in xylene thereby releasing its strain energy[clarification needed].

See also

References

  1. ^ McCarthy, M. C.; Yu, Z.; Sari, L.; Schaefer, H. F.; Thaddeus, P. (15 February 2006). "Monobridged Si2H4". The Journal of Chemical Physics. 124 (7). USA: American Institute of Physics: 074303. Bibcode:2006JChPh.124g4303M. doi:10.1063/1.2168150. PMID 16497032.
  2. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  3. ^ Fused Tricyclic Disilenes with Highly Strained Si-Si Double Bonds: Addition of a Si-Si Single Bond to a Si-Si Double Bond Ryoji Tanaka, Takeaki Iwamoto, and Mitsuo Kira Angewandte Chemie International Edition Volume 45, Issue 38 , Pages 6371 - 6373 2006 doi:10.1002/anie.200602214
  • v
  • t
  • e
Alkali metal
(Group 1) hydridesAlkaline
(Group 2)
earth hydrides
Monohydrides
Dihydrides
  • BeH2
  • MgH2
  • CaH2
  • SrH2
  • BaH2
Group 13
hydrides
Boranes
  • BH3
  • BH
  • B2H6
  • B2H2
  • B2H4
  • B4H10
  • B5H9
  • B5H11
  • B6H10
  • B6H12
  • B10H14
  • B18H22
Alanes
  • AlH3
  • Al2H6
Gallanes
  • GaH3
  • Ga2H6
Indiganes
  • InH3
  • In2H6
Thallanes
  • TlH3
  • Tl2H6
Nihonanes (predicted)
  • NhH
  • NhH3
  • Nh2H6
  • NhH5
Group 14 hydrides
Hydrocarbons
  • CH
  • CH2
  • CH3
  • C2H
Silanes
  • SiH4
  • Si2H6
  • Si3H8
  • Si4H10
  • Si5H12
  • Si6H14
  • Si7H16
  • Si8H18
  • Si9H20
  • Si10H22
  • more...
Silenes
  • Si2H4
Silynes
Germanes
  • GeH4
  • Ge2H6
  • Ge3H8
  • Ge4H10
  • Ge5H12
Stannanes
  • SnH4
  • Sn2H6
Plumbanes
  • PbH4
Flerovanes (predicted)
  • FlH
  • FlH2
  • FlH4
Pnictogen
(Group 15) hydrides
Azanes
  • NH3
  • N2H4
  • N3H5
  • N4H6
  • N5H7
  • N6H8
  • N7H9
  • N8H10
  • N9H11
  • N10H12
  • more...
Azenes
  • N2H2
  • N3H3
  • N4H4
Phosphanes
  • PH3
  • P2H4
  • P3H5
  • P4H6
  • P5H7
  • P6H8
  • P7H9
  • P8H10
  • P9H11
  • P10H12
  • more...
Phosphenes
  • P2H2
  • P3H3
  • P4H4
Arsanes
  • AsH3
  • As2H4
Stibanes
  • SbH3
Bismuthanes
  • BiH3
Moscovanes
  • McH3 (predicted)
  • HN3
  • NH
  • HN5
  • NH5 (?)
Hydrogen
chalcogenides
(Group 16 hydrides)
Polyoxidanes
  • H2O
  • H2O2
  • H2O3
  • H2O4
  • H2O5
  • more...
  • Polysulfanes
    • H2S
    • H2S2
    • H2S3
    • H2S4
    • H2S5
    • H2S6
    • H2S7
    • H2S8
    • H2S9
    • H2S10
    • more...
    Selanes
    • H2Se
    • H2Se2
    Tellanes
    • H2Te
    • H2Te2
    Polanes
    • PoH2
    Livermoranes
    • LvH2 (predicted)
    • HO
    • HO2
    • HO3
    • H2O+–O (?)
    • HS
    • HDO
    • D2O
    • T2O
    Hydrogen halides
    (Group 17 hydrides)
  • HF
  • HCl
  • HBr
  • HI
  • HAt
  • HTs (predicted)
  • Transition metal hydrides
    • ScH2
    • YH2
    • YH3
    • YH6
    • YH9
    • LuH2
    • LuH3
    • TiH2
    • TiH4
    • ZrH2
    • ZrH4
    • HfH2
    • HfH4
    • VH
    • VH2
    • NbH
    • NbH2
    • TaH
    • TaH2
    • CrH
    • CrH2
    • CrHx
    • FeH
    • FeH2
    • FeH5
    • CoH2
    • RhH2
    • IrH3
    • NiH
    • PdHx (x < 1)
    • PtHx (x< 1)
    • DsH2 (predicted)
    • CuH
    • RgH (predicted)
    • ZnH2
    • CdH2
    • HgH
    • Hg2H2
    • HgH2
    • CnH2 (predicted)
    Lanthanide hydrides
    • LaH2
    • LaH3
    • LaH10
    • CeH2
    • CeH3
    • PrH2
    • PrH3
    • NdH2
    • NdH3
    • SmH2
    • SmH3
    • EuH2
    • GdH2
    • GdH3
    • TbH2
    • TbH3
    • DyH2
    • DyH3
    • HoH2
    • HoH3
    • ErH2
    • ErH3
    • TmH2
    • TmH3
    • YbH2
    • LuH2
    • LuH3
    Actinide hydrides
    • AcH2
    • ThH2
    • ThH4
    • Th4H15
    • PaH3
    • UH3
    • UH4
    • NpH2
    • NpH3
    • PuH2
    • PuH3
    • AmH2
    • AmH3
    • CmH2
    • BkH2
    • BkH3
    • CfH2
    • CfH3
    Exotic matter hydrides