209-69-8Relevant academic research and scientific papers
Azulenylcarbene and Naphthylcarbene Isomerizations. Falling Solid Flash Vacuum Pyrolysis
Kvaskoff, David,Becker, Jürgen,Wentrup, Curt
, p. 5030 - 5034 (2015/05/27)
1-Azulenylcarbene 18 has been generated from 5-(1-azulenyl)tetrazole and the sodium salt of azulene-1-carbaldehyde tosylhydrazone using the falling solid flash vacuum pyrolysis (FS-FVP) method. The principal products, which are also formed from both 1- and 2-naphthylcarbenes, cyclobuta[de]naphthalene 6, cyclopenta[cd]indene 16, and benzofulvenallene 17, are explained in terms of two reaction paths, (a) a rearrangement to benzofulvenyl-7-carbene 13 and (b) a rearrangement to 1-naphthylcarbene 1. Moreover, 16 is also formed from 2-azulenylcarbene 30, thereby indicating the occurrence of a 2-azulenylcarbene-1-azulenylcarbene rearrangement. The reaction mechanisms are supported by density functional theory calculations at the B3LYP/6-31G?? level, which indicate that all the rearrangements have activation barriers of 35 kcal/mol, thus making them readily achievable under FVP conditions. Chemical Presented.
Detection of the 1,2-Didehydronaphthalene to 1H-Indenylidenecarbene Rearrangement by Intramolecular Trapping in a Flash Vacuum Pyrolytic Reaction
Brown, Roger F. C.,Coulston, Karen J.,Eastwood, Frank W.,Saminathan, Sugirtham
, p. 107 - 120 (2007/10/02)
Flash vacuum pyrolysis of 9-methyl-1,3-dihydronaphthofuran-1,3-dione (8) at 750-880 deg gave exclusively 1H-cyclopentindene (9) and of 8-methyl-1,2-dihydrocyclobutanaphthalene-1.2-dione (10) at 600-840 deg gave a mixture of (9) and acenaphthylene.Acenaphthylen-4-ol (12) was synthesized and found to be stable to flash vacuum pyrolysis over the temperature range 600-900 deg.These findings are discussed in relation to the rearrangement described in the title.
FORCE FIELD-SCF CALCULATIONS ON CYCLOPROPENE INTERMEDIATES IN CARBENE REARRANGEMENTS. COMPARISON WITH EXPERIMENT
Wentrup, Curt,Mayor, Claude,Becker, Juergen,Lindner, Hans Joerg
, p. 1601 - 1612 (2007/10/02)
Heats of formation and geometries of benzocyclopropene, cyclopropa(b)naphthalene, bicyclo(4.1.0)hepta-2,4,7-triene, and benzannelated derivatives have been calculated with a combined force field-SCF progrsm.The bicycloheptatrienes are stabilized relative to the isomeric arylcarbenes by benzannelation, and destabilized by loss of aromaticity and/or increased strain. 1-Naphthylcarbene, 2-naphthylcarbene, 9-phenanthrylcarbene and 9-anthrylcarbene were generated by gas-phase pyrolysis of the corresponding arene aldehyde tosylhydrazone sodium salts, diazomethanes, or 5-aryltetrazoles, and rearranged to cyclobutanaphthalene(21), cyclobutaphenanthrene(33), and cyclobutaanthracene(38), respectively. 10,11-Dihydrodibenzocyclohepten-5-ylidene (15), similarly generated from 5-diazo-10,11-dihydro-5H-dibenzocycloheptene (39), rearranged to 5a,9b-dihydro-5H-benzocyclobutindene(40), 5H-dibenzocycloheptene(41), and 8,9-dihydro-4H-cyclopentaphenanthrene(40). 40 rearranged thermally to 41.The mechanisms of the rearrangements are discussed.
