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FERROCENYLMETHYLATION OF 1,1-DIARYLALKENES

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Date Issued:
1977
Summary:
The ferrocenylrnethylation of the following compounds was studied using (ferrocenylmethyl)trimethylammonium iodide: 1, 1-di(p-anisyl)- ethene (I), 1, 1-di(p- anisyl)propene (II), 1- (p- anisyl)-1-phenylethene (III), 1, 1- diphenylethene (IV), 1, 1- di(p- dimethylaminophenyl )ethene (V) and 1, 1-di(p-dimethylaminophenyl)propene (VI). I is ferrocenylmethylated exclu,sively on its side-chain, one or both vinyl hydrogens being replaced by ferrocenylmethyl groups depending on the ratio of ferrocenylmethylating agent to I, concentration of the reaction mixture, reaction time, solvent and temperature. II is substituted only on its side-chain to give a mono-ferrocenylmethylated product. III is ferrocenylmethylated slowly. IV fails to react. Mono-ferrocenylmethylation of V occurs principally on its side- chain; more extensive ferrocenylmethylation occurs both on the side-chain and on the rings at the position ortho to dimethylamino. VI reacts quite indiscriminately both on the side-chain and on the rings.
Title: FERROCENYLMETHYLATION OF 1,1-DIARYLALKENES.
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Name(s): FERNANDEZ, ROSA MIRTA
Florida Atlantic University, Degree Grantor
Type of Resource: text
Genre: Electronic Thesis Or Dissertation
Issuance: monographic
Date Issued: 1977
Publisher: Florida Atlantic University
Place of Publication: Boca Raton, Fla.
Physical Form: application/pdf
Extent: 207 p.
Language(s): English
Summary: The ferrocenylrnethylation of the following compounds was studied using (ferrocenylmethyl)trimethylammonium iodide: 1, 1-di(p-anisyl)- ethene (I), 1, 1-di(p- anisyl)propene (II), 1- (p- anisyl)-1-phenylethene (III), 1, 1- diphenylethene (IV), 1, 1- di(p- dimethylaminophenyl )ethene (V) and 1, 1-di(p-dimethylaminophenyl)propene (VI). I is ferrocenylmethylated exclu,sively on its side-chain, one or both vinyl hydrogens being replaced by ferrocenylmethyl groups depending on the ratio of ferrocenylmethylating agent to I, concentration of the reaction mixture, reaction time, solvent and temperature. II is substituted only on its side-chain to give a mono-ferrocenylmethylated product. III is ferrocenylmethylated slowly. IV fails to react. Mono-ferrocenylmethylation of V occurs principally on its side- chain; more extensive ferrocenylmethylation occurs both on the side-chain and on the rings at the position ortho to dimethylamino. VI reacts quite indiscriminately both on the side-chain and on the rings.
Identifier: 13837 (digitool), FADT13837 (IID), fau:10665 (fedora)
Note(s): Thesis (M.S.)--Florida Atlantic University, 1977.
Subject(s): Chemistry--Research
Chemistry, Organic
Methylation
Held by: Florida Atlantic University Libraries
Persistent Link to This Record: http://purl.flvc.org/fcla/dt/13837
Sublocation: Digital Library
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Host Institution: FAU
Is Part of Series: Florida Atlantic University Digital Library Collections.