Quadricyclane

Quadricyclane

Names
Other names quadricyclo[2.2.1.02,6.03.5]heptane, tetracyclo[2.2.1.02,6.03,5]heptane
Identifiers
CAS Registry Number	278-06-8 Y
ChemSpider	30796462
InChI InChI=1S/C7H8/c1-2-4-5(2)7-3(1)6(4)7/h2-7H,1H2/t2-,3+,4+,5-,6+,7- Key: DGZUEIPKRRSMGK-BEOVHNCFSA-N InChI=1/C7H8/c1-2-4-5(2)7-3(1)6(4)7/h2-7H,1H2/t2-,3+,4+,5-,6+,7- Key: DGZUEIPKRRSMGK-BEOVHNCFBK
Jmol-3D images	Image
PubChem	78961
SMILES C1C2C3C2C4C1C34
Properties
Chemical formula	C7H8
Molar mass	92.14 g/mol
Density	0.982 g/cm3
Melting point	−44 °C (−47 °F; 229 K)
Boiling point	108 °C (226 °F; 381 K) at 987 hPa
Solubility in water	Insoluble
Hazards
R-phrases	R11 R23
S-phrases	S16 S29 S33 S45
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
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Infobox references

Quadricyclane is a strained, multi-cyclic hydrocarbon with potential uses as an additive for rocket propellants as well in solar energy conversion. These uses are limited, however, by the molecule's decomposition at relatively low temperatures (less than 400 °C).

Structure and properties

Quadricyclane is a highly strained molecule (78.7 kcal/mol). Isomerization of quadricyclane proceeds slowly at low temperatures without the use of a catalyst.^[1] Because of quadricyclane’s strained structure and thermal stability, it has been studied extensively.

In the presence of a catalyst norbornadiene is converted into quadricyclane via ~300nm UV radiation .^[2] When converted back to norbornadiene via irradiation, quadryicyclane’s ring strain energy is liberated in the form of heat (ΔH = −89 kJ/mol). This reaction has been proposed to store solar energy.^[3][4] However, the absorption edge of light does not extend past 300 nm whereas most solar radiation has wavelengths longer than 400 nm. Quadricyclane’s relative stability and high energy content have also given rise to its use as a propellant additive or fuel. However, quadricyclane undergoes thermal decomposition at relatively low temperatures (less than 400 °C). This property limits its applications, as propulsion systems may operate at temperatures exceeding 500 °C.^[5]

Preparation

Quadricyclane is produced by the irradiation of norbornadiene (bicyclo[2.2.1]hepta-2,5-diene) in the presence of Michler's ketone or ethyl Michler's ketone.^[6] Other sensitizers, such as acetone, benzophenone, acetophenone, etc., may be used but with a lesser yield. The yield is higher for freshly distilled norbornadiene, but commercial reagents will suffice.^[7]

Reactions

Quadricyclane readily reacts with acetic acid to give a mixture of nortricyclyl acetate and exo-norbornyl acetate.^[1] Quadricyclane also reacts with many dienophiles to form 1:1 adducts.^[7]

Notes

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