Hostname: page-component-78c5997874-lj6df Total loading time: 0 Render date: 2024-11-19T06:00:50.901Z Has data issue: false hasContentIssue false
  • English
  • Français

Investigations of a New Reversible Strain Induced Chromic Transition in Polydiacetylene Elastomers

Published online by Cambridge University Press:  25 February 2011

R. A. Nallicheri  and
M. F. Rubner
R. A. Nallicheri
Affiliation:
Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA
M. F. Rubner
Affiliation:
Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA
Get access

Abstract

In-situ visible dichroism/tensile elongation studies of segmented polyurethanes containing conjugated polydiacetylene chains within their hard segment domains have revealed a new reversible mechanochromic transition that manifests itself as a color change from blue to yellow during tensile elongation. This unusual strain induced transition, found in an elastomer whose hard segment structure is derived from hexamethylene diisocyanate and 5,7-dodecadiyne-l,12 diol, closely resembles the thermochromic transition also exhibited by this same material. The color change and the associated shift in the position of the polydiacetylene absorption band to higher energies is not simply an order-disorder transition but reflects a strain induced reorganization of the hard domain structure. It has been found that this blue to yellow transition is reversible as long as the material is not strained beyond about 300%. This represents the first reversible, mechanically induced chromic transition in a cross-polymerized diacetylene containing polymer.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 173: Symposium Q – Advanced Organic Solid State Materials , 1989 , 577
Copyright
Copyright © Materials Research Society 1990

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1. See for example, Bloor, D. and Hubble, C. L., Chem. Phys. Lett. 56, 89 (1978).CrossRefGoogle Scholar
2. Rubner, M. F., Macromolecules 19, 2129 (1986).CrossRefGoogle Scholar
3. Nallicheri, R. A. and Rubner, M.F., Macromolecules, in press.Google Scholar
4. Rubner, M.F., Macromolecules 19, 2114 (1986).Google Scholar
5. Rubner, M. F., Velazquez, C., Sandman, D. J., Macromolecules 20, 1296 (1987).Google Scholar
6. Tanaka, H., Gomez, M. A., Tonelli, A. E., Thakur, M., Macromolecules 22, 1208 (1989).Google Scholar