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  2. Chlorobis(cyclooctene)iridium dimer - Wikipedia

    en.wikipedia.org/wiki/Chlorobis(cyclooctene...

    Chlorobis(cyclooctene)iridium dimer is an organoiridium compound with the formula Ir 2 Cl 2 (C 8 H 14) 4, where C 8 H 14 is cis-cyclooctene.Sometimes abbreviated Ir 2 Cl 2 (coe) 4, it is a yellow, air-sensitive solid that is used as a precursor to many other organoiridium compounds and catalysts.

  3. Cyclooctane - Wikipedia

    en.wikipedia.org/wiki/Cyclooctane

    The activation of these catalysts under H 2, produces cyclooctane, which is usually discarded or burnt: C 8 H 12 + 2 H 2 → C 8 H 16. Cyclooctane participates in no reactions except those typical of other saturated hydrocarbons, combustion and free radical halogenation. Work in 2009 on alkane functionalisation, using peroxides such as dicumyl ...

  4. Cyclooctanone - Wikipedia

    en.wikipedia.org/wiki/Cyclooctanone

    This organic chemistry article is a stub. You can help Wikipedia by expanding it.

  5. Crabtree's catalyst - Wikipedia

    en.wikipedia.org/wiki/Crabtree's_catalyst

    Crabtree's catalyst is an organoiridium compound with the formula [C 8 H 12 IrP(C 6 H 11) 3 C 5 H 5 N]PF 6.It is a homogeneous catalyst for hydrogenation and hydrogen-transfer reactions, developed by Robert H. Crabtree.

  6. C4-Benzenes - Wikipedia

    en.wikipedia.org/wiki/C4-Benzenes

    The C 4-benzenes are a class of organic aromatic compounds which contain a benzene ring and four other carbon atoms. There are three tetramethylbenzenes, six dimethylethylbenzenes, three diethylbenzenes, three isopropylmethylbenzenes, three n-propylmethylbenzenes and four butylbenzenes.

  7. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    Norbornane (also called bicyclo[2.2.1]heptane). Unsubstituted cycloalkanes that contain a single ring in their molecular structure are typically named by adding the prefix "cyclo" to the name of the corresponding linear alkane with the same number of carbon atoms in its chain as the cycloalkane has in its ring.

  8. Cyclodecane - Wikipedia

    en.wikipedia.org/wiki/Cyclodecane

    Print/export Download as PDF; Printable version; In other projects ... Density: 0.871 g/cm 3: Melting point: 9 to 10 °C (48 to 50 °F; 282 to 283 K)

  9. trans-Cyclooctene - Wikipedia

    en.wikipedia.org/wiki/Trans-Cyclooctene

    trans-Cyclooctene was first synthesized on a preparatory scale by Arthur C. Cope with a Hofmann elimination reaction of N,N,N-trimethylcyclooctylammonium iodide. [10] The reaction gives a mixture of cis and trans isomers, and the trans isomer is selectively trapped as a complex with silver nitrate.