Characterization and chemistry of vinylketene prepared by flash vacuum pyrolysisstudy of the flash vacuum pyrolysis of hydroaromatic compounds: 5,8-diphenyltetralin and the parent and substituted 5,6,11,12-tetrahydrodibenzo[a,e]cyclooctenes
dc.contributor.author | Surber, Bruce | |
dc.contributor.department | Department of Chemistry | |
dc.date | 2018-08-16T05:34:06.000 | |
dc.date.accessioned | 2020-07-02T06:02:24Z | |
dc.date.available | 2020-07-02T06:02:24Z | |
dc.date.copyright | Sun Jan 01 00:00:00 UTC 1984 | |
dc.date.issued | 1984 | |
dc.description.abstract | <p>Flash vacuum pyrolysis (FVP) has been used successfully to discover some novel thermal reactions. These provide new insights into some fundamental chemistry;In part I, benzocyclobutene (9) and its 4+4 dimer, 1,5-dibenzocyclooctadiene (14) were found to give anthracene (7) as a major product. The similarity of the product mixtures is taken as evidence that essentially the same mechanism is operating in both cases. By labeling studies, the 4+2 spirodimer (14') appears to be an intermediate. The fragmentation by which 14' is thought to give 7 is new and analogous to the retroene reaction. The proposed mechanism lends new insight into the mechanism of the pyrolytic formation of benzene and higher aromatics;In part II, vinylketene (66), prepared by FVP, was characterized by low-temperature ('1)H- and ('13)C-NMR spectroscopy. It was found to dimerize by a novel 4+2 cyclo-addition reaction. The resulting (delta)-lactone (90) was isomerized to a mixture of sibirinone (91) and 6-allyl-(alpha)-pyrone (92). Acid-catalyzed isomerization gave primarily 91 (9:1 mole ratio). When vinylketene was mixed with cyclopentadiene, the 2+2 cycloadduct (72) was formed with high regio- and stereospecificity. Compound 72 was isomerized to bicyclo4.2.1nona-3,7-dien-2-one (97);Part III described an attempt to determine the effect of surface catalysis in FVP. The synthesis of 5,8-diphenyltetralin (9) was described. Comparison of the pyrolysis of 9 to that of the parent compound, tetralin (1) was not possible since the thermal chemistry of 9 was found to be too different from that of 1. The major product of the pyrolysis of 9 at 1000(DEGREES)C and 10('-5) torr was due to the loss of;C(,2)H(,6) while 1 gave styrene as the major product by the loss of C(,2)H(,4) under similar conditions; *DOE Report IS-T-1111. This work was performed under contract No. W-7405-Eng-82 with the U.S. Department of Energy.</p> | |
dc.format.mimetype | application/pdf | |
dc.identifier | archive/lib.dr.iastate.edu/rtd/7731/ | |
dc.identifier.articleid | 8730 | |
dc.identifier.contextkey | 6323666 | |
dc.identifier.doi | https://doi.org/10.31274/rtd-180813-5386 | |
dc.identifier.s3bucket | isulib-bepress-aws-west | |
dc.identifier.submissionpath | rtd/7731 | |
dc.identifier.uri | https://dr.lib.iastate.edu/handle/20.500.12876/80641 | |
dc.language.iso | en | |
dc.source.bitstream | archive/lib.dr.iastate.edu/rtd/7731/r_8423677.pdf|||Sat Jan 15 01:53:13 UTC 2022 | |
dc.subject.disciplines | Organic Chemistry | |
dc.subject.keywords | Chemistry | |
dc.subject.keywords | Organic chemistry | |
dc.title | Characterization and chemistry of vinylketene prepared by flash vacuum pyrolysisstudy of the flash vacuum pyrolysis of hydroaromatic compounds: 5,8-diphenyltetralin and the parent and substituted 5,6,11,12-tetrahydrodibenzo[a,e]cyclooctenes | |
dc.type | dissertation | |
dc.type.genre | dissertation | |
dspace.entity.type | Publication | |
relation.isOrgUnitOfPublication | 42864f6e-7a3d-4be3-8b5a-0ae3c3830a11 | |
thesis.degree.level | dissertation | |
thesis.degree.name | Doctor of Philosophy |
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