Generation, observation, and free radical reactivity of aliphatic bisketenes: the solution to a long-standing problem.

[reaction: see text] Bisketenes O=C=CH(CH(2))(n)()CH=C=O (1b,c,d, n = 4, 3, 6) and (E)-O=C=CHCH=CHCH=C=O (E-13) were generated in solution by dehydrochlorination of bis(acyl chlorides) and by photochemical Wolff rearrangements and identified by their characteristic IR signals. The bisketenes react with aminoxyl radicals to give tetraaddition products for 1b and conjugate 1,6-diaddition for E-13.

Radical additions of TEMPO to ketenes: correlation of free radical and nucleophilic reactivity.

[reaction: see text] Tetramethylpiperidinyloxy (TEMPO, TO*) reacts with a variety of ketenes R1R2C=C=O by rate-limiting attack on carbonyl carbon to give the 1,2-bis(adducts) R1R2C(OT)CO2T. The alpha,beta-unsaturated ketenes (E)-PhCH=CHCH=C=O (8b) and PhC=CCH=C=O (8c) give the 1,4-bis(adducts) PhCH(OT)CH=CHCO2T and PhC(OT)=C=CHCO2T. The ketenes may be generated in situ for these reactions in the presence of TEMPO by either dehydrochlorination of R1R2CHCOCl with Et3N or Wolff rearrangement. Ketenes PhCH=C=O (8a), 8b, and 8c had not previously been observed as long-lived species at room temperature, but when formed by photochemical Wolff rearrangement, these could be characterized in solution by conventional IR spectroscopy and used for kinetic studies for reaction with TEMPO using UV detection. The reactions of six ketenes with TEMPO in hydrocarbon solvents follow second-order kinetics, with a range of 2.5 x 10(5) in the rate constants, which are correlated with unit slope with the corresponding rate constants for hydration.

A doubly destabilized antiaromatic cyclopentadienyl cation: solvolysis of a 5-trifluoroacetoxy-5-heptafluoropropyl 1,3-cyclopentadiene.

The 5-trifluoroacetoxy-5-heptafluoropropylcyclopentadiene 15 rearranges to the isomeric trifluoroacetate 16 with a rate constant 5 x 10(5) less than that for solvolysis of the corresponding 5-CH(3) derivative 5. Labeling of 15 with (18)O shows the rearrangement occurs by a [1,5]-sigmatropic rearrangement. Solvolysis of 16 occurs at a rate 4 times slower than its formation from 15 and leads to the extensively rearranged fulvene 18, implicating formation of the doubly destabilized cation 20. Carbocation formation from 15 is retarded by a factor of 10(20) relative to the model 11, showing cumulative destabilizing effects due to formation of the antiaromatic cyclopentadienyl carbocation and electron withdrawal by the fluoroalkyl group.

Nitroxyl radical addition to pentafulvenones forming cyclopentadienyl radicals: a test for cyclopentadienyl radical destabilization.

Photochemical Wolff rearrangements in alkane solvents of the 6-diazo-2,4-cyclohexadienones 4 and 13-15 give pentafulvenone (1), 2,3-benzopentafulvenone (2), dibenzopentafulvenone (3), and 2,4-di-tert-butylpentafulvenone (16), as identified by conventional UV and IR spectroscopy. Reactions of these fulvenyl ketenes with tetramethylpiperidinyloxyl (TEMPO) proceed by addition of TEMPO to the carbonyl carbon forming delocalized radicals for 1 and 2 which add one or more further TEMPO molecules, while the initial radical products formed from 3 and 16 dimerize. The rate constants of these reactions compared to hydration rate constants for the same compounds show the benzannulated derivatives 2 and 3 fit a previous correlation k(2)(TEMPO) vs k((H(2)O), whereas for 1 and 16 there is evidence for inhibition of reactions with radicals. The deviations are consistent with an absence of aromatic stabilization of the cyclopentadienyl radicals from 1 and 16 that is compensated in the benzannulated derivatives.

Nitroxyl radical reactions with 4-pentenyl- and cyclopropylketenes: new routes to 5-hexenyl- and cyclopropylmethyl radicals.

4-Pentenylketenes 4a and 9 and cyclopropylketenes 3a, 13, 14 (RCH=C=O) are generated by photochemical Wolff rearrangements and observed by IR as relatively long-lived species at room temperature in hydrocarbon solvents. The reactions of these ketenes with the nitroxyl radicals tetramethylpiperidinyloxyl (TEMPO, TO*) and tetramethylisoindoline-2-oxyl (TMIO, IO*) form carboxy substituted 5-hexenyl and cyclopropylmethyl radicals which are either trapped by a second nitroxyl radical or undergo rearrangements followed by trapping. The rate constant of the reaction of 4a with TEMPO was similar to that of n-BuCH=C=O (1b), while 3a was 4.3 times more reactive, indicating cyclopropyl stabilization of the incipient radical.

Ketene reactions with the aminoxyl radical tempo: preparative, kinetic, and theoretical studies.

Tetramethylpiperidinyloxy (TEMPO, TO*) reacts with ketenes RR(1)C=C=O generated by either Wolff rearrangement or by dehydrochlorination of acyl chlorides to give products resulting from addition of one TEMPO radical to the carbonyl carbon and a second to the resulting radical. Reactions of phenylvinylketenes 4b and 4f, phenylalkynylketene 4c, and the dienylketene AcOCMe=CHCH=CHCMe=C=O (11) occur with allylic or propargylic rearrangement. Even quite reactive ketenes were generated as rather long-lived species by photochemical Wolff rearrangement in isooctane solution, characterized by IR and UV, and used for kinetic studies. The rate constants of TEMPO addition to eight different ketenes have been measured and give a qualitative correlation of log k(2)(TEMPO) = 1.10 log k(H(2)O) -3.79 with the rate constants for hydration of the same ketenes. Calculations at the B3LYP/6-311G//B3LYP/6-311G level are used to elucidate the ring opening of substituted cyclobutenones leading to vinylketenes and of 2,4-cyclohexadienone (17) forming 1,3,5-hexatrien-1-one (18).