For the last decade, the Trahanovsky research group has focused on the study of various reactive molecules such as o-quinodimethanes (o-QDM`s) and p-quinodimethanes (p-QDM`s) derived from benzene, furan, and thiophene. These types of molecules are reactive and dimerize or polymerize at room temperature. One of the group`s interests is to understand the dimerization mechanism of these molecules. Paper 1 describes the preparation and dimerization product analyses of 2-ethylidene-5-methylene-2,5-dihydrothiophene. Insights provided by these results into the mechanism of the dimerization of 2,5-dimethylene-2,5-dihydrothiophene are discussed. In paper 2, a convenient synthesis of cyclooctadecane is presented.
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Description
For the last decade, the Trahanovsky research group has focused on the study of various reactive molecules such as o-quinodimethanes (o-QDM`s) and p-quinodimethanes (p-QDM`s) derived from benzene, furan, and thiophene. These types of molecules are reactive and dimerize or polymerize at room temperature. One of the group`s interests is to understand the dimerization mechanism of these molecules. Paper 1 describes the preparation and dimerization product analyses of 2-ethylidene-5-methylene-2,5-dihydrothiophene. Insights provided by these results into the mechanism of the dimerization of 2,5-dimethylene-2,5-dihydrothiophene are discussed. In paper 2, a convenient synthesis of cyclooctadecane is presented.
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97 p.
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OSTI as DE94014232; Paper copy available at OSTI: phone, 865-576-8401, or email, reports@adonis.osti.gov
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Wang, Yili.The mechanism of the oligomerization of thiophene-based para-quinodimethanes,
thesis or dissertation,
April 24, 1994;
Iowa.
(https://digital.library.unt.edu/ark:/67531/metadc1388345/:
accessed July 16, 2024),
University of North Texas Libraries, UNT Digital Library, https://digital.library.unt.edu;
crediting UNT Libraries Government Documents Department.
