128937-89-3Relevant academic research and scientific papers
Construction and molecular understanding of an unprecedented, reversibly thermochromic bis-polydiacetylene
Lee, Songyi,Lee, Joonseong,Lee, Minji,Cho, Yu Kyung,Baek, Junwoo,Kim, Jinwook,Park, Sungnam,Kim, Myung Hwa,Chang, Rakwoo,Yoon, Juyoung
, p. 3699 - 3705 (2014)
A new type of bis-PDA, in which two PDAs are linked via an intervening p-phenylene group, is developed. The Bis-PDA-Ph displays exceptional thermochromic reversibility owing to the presence of unique hydrophobic interactions between alkyl chains as well as aryl moieties. The Bis-PDA-Ph has a well-packed structure that causes it to display a clear blue to red colorimetric transition at elevated temperatures. To elucidate the molecular origin of the thermochromic response, a theoretical simulation of the new PDA, the results of which successfully explain the thermochromic reversibility phenomenon, is conducted. Furthermore, Bis-PDA-Ph-embedded polymer fibers are used as a thermochromic sensor material. It displays excellent reversibility between 20-120 °C, which is the largest temperature range reported thus far for PDA based sensors. Finally, transient absorption spectroscopy is employed for the first time to analyze the temperature-dependent fluorescence change of the new PDA. The Bis-PDA-Ph (two PDAs are linked via an intervening p-phenylene group) displays exceptional thermochromic reversibility with a blue to red colorimetric transition at elevated temperatures. To elucidate the molecular origin of the thermochromic response, a theoretical simulation of the new PDA which explains the reversibility phenomenon, is conducted. Furthermore, Bis-PDA-Ph-embedded fibers display excellent reversibility between 20-120 °C.
REACTION OF DIYNOYL CHLORIDES WITH PARA-SUBSTITUTED PHENOLS
Budilova, I. Yu.,Kolesnikov, A. M.,Kolotilo, N. V.,Il'chenko, A. Ya.
, p. 264 - 267 (2007/10/02)
The reaction of diynoyl chlorides with para-substituted phenols was studied.As a result amphiphilic diacetylenic compounds containing an aromatic ring in the chain, which are of interest for the production of Langmuir-Blodgett films, were obtained.
