4.1 Article Proceedings Paper

Reversed photochromism reactivity of malononitrile attached bisthienylthene

Journal

MOLECULAR CRYSTALS AND LIQUID CRYSTALS
Volume 662, Issue 1, Pages 147-156

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/15421406.2018.1466534

Keywords

Bisthienylethene; malononitrile; photo- and thermal-stability; photocyclizing atoms; reversed photochromism

Funding

  1. National Natural Science Foundation of China [21272060, 21772034]
  2. Program for Innovative Research Team in Science and Technology in University of Henan Province [15IRTSTHN003]
  3. National Research Foundation of Korea (NRF) - Ministry of Science, ICT and Future Planning [NRF-2017R1E1A1A01074266]
  4. National Research Foundation of Korea [22A20130000149] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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An electron acceptor, malononitrile, was attached to bisthienylethene derivative. The significant influence of electron nature result a reversed phtochromism. Investigation of MT in THF demonstrates the reversible ring-open and ring-close. Upon irradiation of 405nm laser, the solution color changed from yellowish to colorless, which is different from most of the photochromic colored phenomenon. Upon 254nm irradiation, the original yellowish state can be recovered. Due to the attachment of malononitrile, the photo-/thermal-stability were enhanced. The ring-open/ring-closed forms were optimized by Dmol(3). The distance between photocyclizing atoms in aptiparallel conformation meets the requirement for photochromic reaction. And the calculated absorption values were also in agreement with the experimental ones.

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