CaltechTHESIS
  A Caltech Library Service

I. The Effect of N,N,N',N'-Tetramethylethylenediamine on the Schlenk Equilibrium. II. The Nature of the Di-Grignard Reagent

Citation

Magnuson, James Andrew (1968) I. The Effect of N,N,N',N'-Tetramethylethylenediamine on the Schlenk Equilibrium. II. The Nature of the Di-Grignard Reagent. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/0CT8-7385. https://resolver.caltech.edu/CaltechTHESIS:12182015-155008048

Abstract

I. The influence of N,N,N’,N’-tetramethylethylenediamine on the Schlenk equilibrium

The equilibrium between ethylmagnesium bromide, diethylmagnesium, and magnesium bromide has been studied by nuclear magnetic resonance spectroscopy. The interconversion of the species is very fast on the nmr time scale, and only an averaged spectrum is observed for the ethyl species. When N,N,N’,N’-tetramethylethylenediamine is added to solutions of these reagents in tetrahydrofuran, the rate of interconversion is reduced. At temperatures near -50°, two ethylmagnesium species have been observed. These are attributed to the different ethyl groups in ethylmagnesium bromide and diethylmagnesium, two of the species involved in the Schlenk equilibrium of Grignard reagents.

II. The nature of di-Grignard reagents

Di-Grignard reagents have been examined by nuclear magnetic resonance spectroscopy in an attempt to prove that dialkylmagnesium reagents are in equilibrium with alkylmagnesium halides. The di-Grignard reagents of compounds such as 1,4-dibromobutane have been investigated. The dialkylmagnesium form of this di-Grignard reagent can exist as an intramolecular cyclic species, tetramethylene-magnesium. This cyclic form would give an nmr spectrum different from that of the classical alkylmagnesium halide di-Grignard reagent. In dimethyl ether-tetrahydrofuran solutions of di-Grignard reagents containing N N,N,N’,N’-Tetramethylethylenediamine, evidence has been found for the existence of an intramolecular dialkylmagnesium species. This species is rapidly equilibrating with other forms, but at low temperatures, the rates of interconversion are reduced. Two species can be seen in the nmr spectrum at -50°. One is the cyclic species; the other is an open form.

Inversion of the carbon at the carbon-magnesium bond in di-Grignard reagents has also been studied. This process is much faster than in corresponding monofunctional Grignard reagents.

Item Type:Thesis (Dissertation (Ph.D.))
Subject Keywords:(Chemistry)
Degree Grantor:California Institute of Technology
Division:Chemistry and Chemical Engineering
Major Option:Chemistry
Thesis Availability:Public (worldwide access)
Research Advisor(s):
  • Roberts, John D.
Thesis Committee:
  • Unknown, Unknown
Defense Date:7 September 1967
Record Number:CaltechTHESIS:12182015-155008048
Persistent URL:https://resolver.caltech.edu/CaltechTHESIS:12182015-155008048
DOI:10.7907/0CT8-7385
Default Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:9330
Collection:CaltechTHESIS
Deposited By:INVALID USER
Deposited On:21 Dec 2015 17:39
Last Modified:03 Apr 2024 21:25

Thesis Files

[img]
Preview
PDF - Final Version
See Usage Policy.

24MB

Repository Staff Only: item control page