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Tricyclo decatriene

Anhydrous silver-olefin complexes are readily dissociable, low-melting, and variable in composition 92a, 176, 183). Cyclic olefins and polyolefins form stable complexes with silver nitrate or perchlorate, but again the Stoichiometry of the complexes varies considerably, sometimes depending on the conditions of preparation. The following types have been isolated [Ag(un)2]X (un = e.g., cyclohexene, a- and /3-pinene) ISO), [Ag(diene)]X diene = e.g., dicyclopentadiene 220), cyclo-octa-1,5-diene 50, 130), bi-cyclop, 2,1 ]hepta-2,5-diene 207), and cyclo-octa-1,3,5-triene 52), and [Ag2(diene)]X2 (diene = e.g., cyclo-octa-1,3- and -1,4-diene 180), bi-cyclo[2,2,l]hepta-2,5-diene 1) and tricyclo[4,2,2,0]-decatriene 10)). Cyclo-octatetraene (cot) forms three adducts with silver nitrate 52), viz., [Ag(cot)]NOs, [Ag(cot)2]N03, and [Ag3(cot)2](N03)3. On heating, the first two lose cyclo-octatetraene and all three decompose at the same temperature. From the stoichiometry of the above complexes it appears that the... [Pg.102]

The conjugated trienes cis. trims,cis-1,3,5-cyclodccalriene (16) and cisjrans,3,5-cycloun-decatriene (17) thermally isomerize with stereospecific formation of the tricyclic alkenes trans-tricyclo[5.3.0.04,6]dec-2-ene (18) and rrany-tricyelo[5.4.0.04-6]undec-2-ene (19) by reactions involving [1,5] sigmalropic hydrogen shifts followed by intramolecular [4 + 2] cycloadditions98. [Pg.1158]

The purely thermal processes that are involved include the formation of cw-9,10-dihydronaphthalene (C9,10) from bullvalene (BV), bicyclo[4.2.2]decatetrene (422) and its intramolecular Diels-Alder adduct, tetracyclo[4.4.0.0 0 ]decadiene (TCD), from lumibullvalene (LBV), isobullvalene (IBV), tricyclo[5.3.0.0 ]deca-3,5,9-triene (TDT), and isolumibullvalene (ILBV), from basketene (BSK), NHC, TRQ, and the syn and anti isomers of tricyclo[4.4.0.0 ]decatriene (S and A, respectively), and from all c/ -cyclodecapentaene (C5), snoutene (SNT), and diademane (DIA). A more recent review includes many heats of formation and enthalpies of activation ... [Pg.331]


See other pages where Tricyclo decatriene is mentioned: [Pg.298]    [Pg.433]    [Pg.811]    [Pg.816]    [Pg.819]    [Pg.832]    [Pg.64]   
See also in sourсe #XX -- [ Pg.331 ]




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1.6.8- Decatriene

Decatrienal

Decatrienes

Tricyclo

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