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Small-Ring Compounds. XXXX. The Structure and Properties of a Dimer of Triphenylfluorocyclobutadiene

Nagarajan, Kuppuswamy and Caserio, Marjorie C. and Roberts, John D. (1964) Small-Ring Compounds. XXXX. The Structure and Properties of a Dimer of Triphenylfluorocyclobutadiene. Journal of the American Chemical Society, 86 (3). pp. 449-453. ISSN 0002-7863. doi:10.1021/ja01057a032. https://resolver.caltech.edu/CaltechAUTHORS:20151016-112437144

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Abstract

The chemistry of the previously described substance, C_(44)H_(30)F_2 from the reaction of 1,1-difluoro-2,4-dichloro-3-phenylcyclobutene and phenyllithium is described. The physical and chemical data presented are best interpreted in terms of an anti-tricyclo[4.2.0.0] octadiene structure for the substance which could arise by dimerization of triphenylfluorocyclobutadiene. The recent X-ray diffraction study of the substance by Hughes and Fritchie has confirmed the proposed structure.


Item Type:Article
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URLURL TypeDescription
http://dx.doi.org/10.1021/ja01057a032DOIArticle
http://pubs.acs.org/doi/abs/10.1021/ja01057a032PublisherArticle
Additional Information:© 1964 American Chemical Society. Received August 26, 1963. Supported in part by the National Science Foundation.
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Other Numbering System:
Other Numbering System NameOther Numbering System ID
Caltech Gates and Crellin Laboratories of Chemistry3006
Issue or Number:3
DOI:10.1021/ja01057a032
Record Number:CaltechAUTHORS:20151016-112437144
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20151016-112437144
Official Citation:Small-Ring Compounds. XXXX. The Structure and Properties of a Dimer of Triphenylfluorocyclobutadiene Kuppuswamy. Nagarajan, Marjorie C. Caserio, and John D. Roberts Journal of the American Chemical Society 1964 86 (3), 449-453 DOI: 10.1021/ja01057a032
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:61204
Collection:CaltechAUTHORS
Deposited By: Ruth Sustaita
Deposited On:16 Oct 2015 21:22
Last Modified:10 Nov 2021 22:45

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