A narrow range multielectrochromism from 2,5-di-(2-thienyl)-1H-pyrrole polymer bearing pendant perylenediimide moiety

Add time:07/24/2019    Source:sciencedirect.com

A new 2,5-di-(2-thienyl)-1H-pyrrole (SNS) moiety containing perylenediimide (PDI) acceptor as pendant side chain has been synthesized for an electroactive monomer and then directly deposited onto ITO/glass surface via electrochemical polymerization process. The observed electronic interaction only at the excited state due to the presence of phenylene spacer between SNS-donor and PDI-acceptor moiety leads to efficient fluorescence quenching. This charge separation behavior was also proved by theoretical DFT calculations. Thin films of the polymer electropolymerized onto transparent electrode exhibited ambipolar multi-electrochromic behavior including purple, violet-red-khaki-blue colors in both anodic and cathodic regime only between −1.2 and 1.0 V. We further demonstrated that this polymer film has a high contrast ratio (ΔT = 45% at 900 nm), a faster response (0.5 s), high coloration efficiency (254 cm2 C−1) and retained its performance by 92% even after 5000 cycles.

We also recommend Trading Suppliers and Manufacturers of 2,5-di(thiophen-2-yl)pyridine (cas 109612-01-3). Pls Click Website Link as below: cas 109612-01-3 suppliers

Prev:Zinc azaphthalocyanines with thiophen-2-yl, 5-methylthiophen-2-yl and pyridin-3-yl peripheral substituents: Additive substituent contributions to singlet oxygen production
Next:Synthesis, computational quantum chemical study, in silico ADMET and molecular docking analysis, in vitro biological evaluation of a novel sulfur heterocyclic thiophene derivative containing 1,2,3-triazole and pyridine moieties as a potential human topoisomerase IIα inhibiting anticancer agent)