1991
DOI: 10.1039/p19910000465
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Generation and reactions of 2-alkoxydiphenylcarbenes in fluid solution and rigid matrices

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Cited by 10 publications
(4 citation statements)
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“…Tomioka et al [18] reported that chemically synthesized 2,3-diphenyl-2, 3-dihydrofuran has a similar pattern in the same region. In the proton NMR spectra, both poly(4HS) and poly(NOHS) showed indistinguishable broad peaks at 6 to 8 ppm in the aromatic region that are characteristics of different and closely packed hydrogens as polymer formed.…”
mentioning
confidence: 94%
“…Tomioka et al [18] reported that chemically synthesized 2,3-diphenyl-2, 3-dihydrofuran has a similar pattern in the same region. In the proton NMR spectra, both poly(4HS) and poly(NOHS) showed indistinguishable broad peaks at 6 to 8 ppm in the aromatic region that are characteristics of different and closely packed hydrogens as polymer formed.…”
mentioning
confidence: 94%
“…Numerous studies have shown that if the ground state of carbenes is triplet, then the efficiency of carbene transformations by the `abstraction ± recombination' mechanism (4) in the transition from the liquid to the solid phase with a decrease in temperature is drastically increased. 38,43,44 The effective constants of the decay rate of triplet carbenes determined experimentally at cryogenic temperatures are very small. For example, they amount to 10 73 ± 10 74 s 71 for different frozen organic matrices (Ref.…”
Section: Assessment Of the Structural-physical Heterogeneity Of Polym...mentioning
confidence: 99%
“…), 113.48, 102.75 (quat. ), 71.59 and 21.66 (CH 3 ); m/z 161 (M ϩ , 9%), 119 (100), 91 (47), 64 (18) and 63 (17).…”
Section: -Isopropoxybenzonitrile 17mentioning
confidence: 99%