Materials-chirality

a simple motion probe of polymeric glassy and rubbery states

Ji Woong Park, Mark M. Green

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Abstract

The 1,1′-Binaphthyl chiral molecule is studied. The thermal racemization of this molecule occurs through rotation about the C(1)-C(1′) bond and follows strictly first order kinetics with a half-life of between 10 and 20 hrs as a function of solvent at 20°C. This racemization can be caused by heat or by irradiation, with the energy flux controlling the extent of racemization. This can be read as a gray scale of response to circularly or plane polarized light which can be read over a wide wavelength range following from the optical rotatory dispersion effect, and stored in an archival manner below Tg.

Original languageEnglish (US)
Title of host publicationAmerican Chemical Society, Polymer Preprints, Division of Polymer Chemistry
Editors Anon
PublisherACS
Pages707-708
Number of pages2
Volume39
Edition2
StatePublished - Aug 1998
EventProceedings of the 1997 Boston Meeting - Boston, MA, USA
Duration: Aug 23 1998Aug 27 1998

Other

OtherProceedings of the 1997 Boston Meeting
CityBoston, MA, USA
Period8/23/988/27/98

Fingerprint

Chirality
Molecules
Light polarization
Irradiation
Fluxes
Wavelength
Kinetics
Hot Temperature

ASJC Scopus subject areas

  • Polymers and Plastics

Cite this

Park, J. W., & Green, M. M. (1998). Materials-chirality: a simple motion probe of polymeric glassy and rubbery states. In Anon (Ed.), American Chemical Society, Polymer Preprints, Division of Polymer Chemistry (2 ed., Vol. 39, pp. 707-708). ACS.

Materials-chirality : a simple motion probe of polymeric glassy and rubbery states. / Park, Ji Woong; Green, Mark M.

American Chemical Society, Polymer Preprints, Division of Polymer Chemistry. ed. / Anon. Vol. 39 2. ed. ACS, 1998. p. 707-708.

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Park, JW & Green, MM 1998, Materials-chirality: a simple motion probe of polymeric glassy and rubbery states. in Anon (ed.), American Chemical Society, Polymer Preprints, Division of Polymer Chemistry. 2 edn, vol. 39, ACS, pp. 707-708, Proceedings of the 1997 Boston Meeting, Boston, MA, USA, 8/23/98.
Park JW, Green MM. Materials-chirality: a simple motion probe of polymeric glassy and rubbery states. In Anon, editor, American Chemical Society, Polymer Preprints, Division of Polymer Chemistry. 2 ed. Vol. 39. ACS. 1998. p. 707-708
Park, Ji Woong ; Green, Mark M. / Materials-chirality : a simple motion probe of polymeric glassy and rubbery states. American Chemical Society, Polymer Preprints, Division of Polymer Chemistry. editor / Anon. Vol. 39 2. ed. ACS, 1998. pp. 707-708
@inproceedings{7188335a03b24dc2955902d8a182ab03,
title = "Materials-chirality: a simple motion probe of polymeric glassy and rubbery states",
abstract = "The 1,1′-Binaphthyl chiral molecule is studied. The thermal racemization of this molecule occurs through rotation about the C(1)-C(1′) bond and follows strictly first order kinetics with a half-life of between 10 and 20 hrs as a function of solvent at 20°C. This racemization can be caused by heat or by irradiation, with the energy flux controlling the extent of racemization. This can be read as a gray scale of response to circularly or plane polarized light which can be read over a wide wavelength range following from the optical rotatory dispersion effect, and stored in an archival manner below Tg.",
author = "Park, {Ji Woong} and Green, {Mark M.}",
year = "1998",
month = "8",
language = "English (US)",
volume = "39",
pages = "707--708",
editor = "Anon",
booktitle = "American Chemical Society, Polymer Preprints, Division of Polymer Chemistry",
publisher = "ACS",
edition = "2",

}

TY - GEN

T1 - Materials-chirality

T2 - a simple motion probe of polymeric glassy and rubbery states

AU - Park, Ji Woong

AU - Green, Mark M.

PY - 1998/8

Y1 - 1998/8

N2 - The 1,1′-Binaphthyl chiral molecule is studied. The thermal racemization of this molecule occurs through rotation about the C(1)-C(1′) bond and follows strictly first order kinetics with a half-life of between 10 and 20 hrs as a function of solvent at 20°C. This racemization can be caused by heat or by irradiation, with the energy flux controlling the extent of racemization. This can be read as a gray scale of response to circularly or plane polarized light which can be read over a wide wavelength range following from the optical rotatory dispersion effect, and stored in an archival manner below Tg.

AB - The 1,1′-Binaphthyl chiral molecule is studied. The thermal racemization of this molecule occurs through rotation about the C(1)-C(1′) bond and follows strictly first order kinetics with a half-life of between 10 and 20 hrs as a function of solvent at 20°C. This racemization can be caused by heat or by irradiation, with the energy flux controlling the extent of racemization. This can be read as a gray scale of response to circularly or plane polarized light which can be read over a wide wavelength range following from the optical rotatory dispersion effect, and stored in an archival manner below Tg.

UR - http://www.scopus.com/inward/record.url?scp=0032140008&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0032140008&partnerID=8YFLogxK

M3 - Conference contribution

VL - 39

SP - 707

EP - 708

BT - American Chemical Society, Polymer Preprints, Division of Polymer Chemistry

A2 - Anon, null

PB - ACS

ER -