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Cyclooctatetraene Cyclooctene

Cyclooctatetraene is relatively stable but lacks the special stability of benzene Unlike benzene which we saw has a heat of hydrogenation that is 152 kJ/mol (36 kcal/mol) less than three times the heat of hydrogenation of cyclohexene cycloocta tetraene s heat of hydrogenation is only 26 kJ/mol (6 kJ/mol) less than four times that of CIS cyclooctene... [Pg.450]

Abbreviations acac, acetylacetonate Aik, alkyl AN, acetonitrile bpy, 2,2 -bipyridine Bu, butyl cod, 1,5- or 1,4-cyclooctadiene coe, cyclooctene cot, cyclooctatetraene Cp, cyclopentadienyl Cp, pentamethylcyclopenladienyl Cy, cyclohexyl dme, 1,2-dimethoxyethane dpe, bis(diphenyl-phosphino)ethane dppen, cis-l,2-bis(di[Atenylphosphino)ethylene dppm, bis(diphenylphosphino) methane dppp, l,3-bis(diphenylphosphino)propane eda,ethylenediamine Et,ethyl Hal,halide Hpz, pyrazole HPz, variously substituted pyrazoles Hpz, 3,5-dimethylpyrazole Me, methyl Mes, mesityl nbd, notboma-2,5-diene OBor, (lS)-endo-(-)-bomoxy Ph, phenyl phen, LlO-phenanthroline Pr, f opyl py, pyridine pz, pyrazolate Pz, variously substituted pyrazolates pz, 3,5-dimethylpyrazolate solv, solvent tfb, tetrafluorobenzo(5,6]bicyclo(2.2.2]octa-2,5,7-triene (tetrafluorobenzobanelene) THE, tetrahydrofuran tht, tetrahydrothicphene Tol, tolyl. [Pg.157]

Abbreviations aapy, 2-acetamidopyridine Aik, alkyl AN, acetoniuile Ar, aryl Bu, butyl cod, 1,5-cyclooctadiene COE, cyclooctene COT, cyclooctatetraene Cp, cyclopentadienyl Cp , penta-methylcyclopentadienyl Cy, cyclohexyl DME, 1,2-dimethoxyethane DME, dimethylformamide DMSO, dimethyl sulfoxide dmpe, dimethylphosphinoethane dppe, diphenylphosphinoethane dppm, diphenylphosphinomethane dppp, diphenylphosphinopropane Et, ethyl Ec, feirocenyl ind, inda-zolyl Me, methyl Mes, mesitylene nb, norbomene orbicyclo[2.2.1]heptene nbd, 2,5-norbomadiene OTf, uiflate Ph, phenyl PPN, bis(triphenylphosphoranylidene)ammonium Pi , propyl py, pyridine pz, pyrazolate pz, substituted pyi azolate pz , 3,5-dimethylpyrazolate quin, quinolin-8-olate solv, solvent tfb, teti afluorobenzobaiTelene THE, tetrahydrofuran THT, tetrahydrothiophene tmeda, teti amethylethylenediamine Tol, tolyl Tp, HB(C3H3N2)3 Tp , HB(3,5-Me2C3HN2)3 Tp, substituted hydrotiis(pyrazol-l-yl)borate Ts, tosyl tz, 1,2,4-triazolate Vin, vinyl. [Pg.167]

Cyclooctatetraene from cubane, 203 point group of, 6 Cyclooctatrienone, 289 co-Cyclooctene IP, 102... [Pg.364]

When ris-cyclooctene is hydrogenated, 96 kjmol 1 of energy is released. Cyclooctatetraene releases 410 kj mol-1 on hydrogenation. This value is approximately four times one double... [Pg.173]

The third route involves metathesis polymerization of cyclooctatetraene with tungsten catalysts, yielding polyacetylene as an insoluble film along with oligomers (iOi). By first polymerizing cyclooctene and then adding cyclooctatetraene, a soluble, red block copolymer was obtained. On the basis of the visible absorption spectrum, at least two or three cyclooctatetraene units were concluded to have been added to the polymer chain forming a short polyacetylene block. No conductivity data were reported for this copolymer. [Pg.289]


See other pages where Cyclooctatetraene Cyclooctene is mentioned: [Pg.16]    [Pg.85]    [Pg.92]    [Pg.243]    [Pg.16]    [Pg.14]    [Pg.54]    [Pg.55]    [Pg.14]    [Pg.256]    [Pg.1042]    [Pg.902]    [Pg.445]    [Pg.320]   


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