Results 41 to 50 of about 7,520 (264)

Highly Efficient Photoswitch in Diarylethene-Based Molecular Junctions.

open access: yesJournal of the American Chemical Society, 2020
Thin layers of diarylethene oligomers (oligo(DAE)) were deposited by electrochemical reduction of a diazonium salt on glassy carbon and gold electrodes. The layers were fully characterized using electrochemistry, XPS, and AFM, and switching between open ...
Imen Hnid   +4 more
semanticscholar   +1 more source

First direct evidence of N-heterocyclic carbene in BMIm acetate ionic liquid. An electrochemical and chemical study on the role of temperature [PDF]

open access: yes, 2017
Cyclic voltammetry provides the first direct evidence of N-­heterocyclic carbene (NHC) presence in neat 1-‐butyl-­3-­methylimidazolium acetate ionic liquid (BMImAcO) at 120°C. The NHC existence, proved by its oxidation current in cyclic voltammetry, was
Chiarotto, I., Feroci, M., Inesi, A.
core   +1 more source

A photochemical determination of luminescence efficiency of upconverting nanoparticles

open access: yesBeilstein Journal of Organic Chemistry, 2019
Upconverting nanoparticles are a rising class of non-linear luminescent probes burgeoning since the beginning of the 2000’s, especially for their attractiveness in theranostics.
Baptiste Amouroux   +4 more
doaj   +1 more source

Mechanochemical Regulation of a Photochemical Reaction [PDF]

open access: yes, 2018
We introduce the concept of mechanochemically gated photoswitching. Mechanical regulation of a photochemical reaction is exemplified using a newly designed mechanophore based on a cyclopentadiene–maleimide Diels–Alder adduct.
Barber, Ross W.   +3 more
core   +4 more sources

Proton‐Gated Ring‐Closure of a Negative Photochromic Azulene‐Based Diarylethene

open access: yesAngewandte Chemie, 2020
Proton‐responsive photochromic molecules are attractive for their ability to react on non‐invasive rapid optical stimuli and the importance of protonation/deprotonation processes in various fields.
I. Hou   +4 more
semanticscholar   +1 more source

Aggregation-induced emission effect on turn-off fluorescent switching of a photochromic diarylethene

open access: yesBeilstein Journal of Organic Chemistry, 2019
Background: Diarylethenes are well-known photochromic compounds, which undergo cyclization and cycloreversion reactions between open- and closed-ring isomers.
Luna Kono   +10 more
doaj   +1 more source

Switching and Rectification of a Single Light-sensitive Diarylethene Molecule Sandwiched between Graphene Nanoribbons

open access: yes, 2011
The 'open' and 'closed' isomers of the diarylethene molecule that can be converted between each other upon photo-excitation are found to have drastically different current-voltage characteristics when sandwiched between two graphene nanoribbons (GNRs ...
Cai, Yongqing   +3 more
core   +1 more source

Photophysics of closed- and open-ring isomers of a diarylethene with a carboxylic anchor group [PDF]

open access: yes, 2012
We study the transient photophysical properties of a diarylethene with a carboxylic anchor group by a combination of steady-state and ultrafast emission and absorption spectroscopy.
Elsaesser, T.   +5 more
core   +1 more source

Investigation of Photochromic Fluorescence Features and Synthesis of Diarylethene Type Naphthalimide Compounds

open access: yesJournal of the Turkish Chemical Society, Section A: Chemistry, 2020
The aim of the study was to synthesise novel photo-exchangeable photochromic fluorescence compounds. Starting from N-butyl-4-bromo-3-iodo-1,8-naphthalimide new compounds: 3,4-Bis(3,5-dimethyl-4-pyrazolyl)-N-butyl-1,8-Naphthalimide 6 and 3,4-Bis (1,3,5 ...
Ersin ORHAN, Mustafa NARİN
doaj   +1 more source

Efficient light-induced phase transitions in halogen-bonded liquid crystals [PDF]

open access: yes, 2016
Here, we present a new family of light-responsive, fluorinated supramolecular liquid crystals (LCs) showing efficient and reversible light-induced LC-to-isotropic phase transitions.
Fernandez-Palacio F.   +8 more
core   +1 more source

Home - About - Disclaimer - Privacy