Claims
- 1. An ethynyl terminated imidothioether having the following structural formula ##STR8## wherein R is selected from the group of divalent radicals consisting of CH.sub.2 CH.sub.2, CH.sub.2 CH.sub.2 CH.sub.2, CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.2, CH.sub.2 OCH.sub.2 OCH.sub.2, ##STR9## wherein X is a bond, or X represents a member selected from the group consisting of CH.sub.2, O, S, C(CH.sub.3).sub.2, C(CF.sub.3).sub.2, SO.sub.2, and O.dbd.C; the ethynyl terminated imidothioether being formed as a mixture of stereoisomers comprising the d, l, and meso forms.
- 2. An ethynyl terminated imidothioether according to claim 1 which is produced by the reaction of a dimercaptan and an ethynyl containing maleimide.
- 3. An ethynyl terminated imidothioether according to claim 2, wherein the dimercaptan is 4,4'-dimercaptodiphenyl ether and the ethynyl containing maleimide in N-(3-ethynylphenyl)maleimide.
ORIGIN OF THE INVENTION
The invention described herein was made jointly in the performance of work under a NASA Grant and an employee of the United States Government. In accordance with 35 USC 202, the grantee elected not to retain title.
US Referenced Citations (2)
Number |
Name |
Date |
Kind |
4282347 |
Tieszen et al. |
Aug 1981 |
|
4365068 |
Darms et al. |
Dec 1982 |
|