Search results for "Diarylethen"

showing 3 items of 13 documents

Light-Activated Sensitive Probes for Amine Detection

2017

Our new, simple, and accurate colorimetric method is based on diarylethenes (DAEs) for the rapid detection of a wide range of primary and secondary amines. The probes consist of aldehyde- or ketone-substituted diarylethenes, which undergo an amine-induced decoloration reaction, selectively to give the ring-closed isomer. Thus, these probes can be activated at the desired moment by light irradiation, with a sensitivity that allows the detection of amines at concentrations as low as 10exp−6 M in solution. In addition, the practical immobilization of DAEs on paper makes it possible to detect biogenic amines, such as cadaverine, in the gas phase above a threshold of 12 ppbv within 30 seconds. P…

amines010402 general chemistryPhotochemistry01 natural sciencesRapid detectionAldehydeCatalysisGas phasechemistry.chemical_compoundsensingchemistry.chemical_classificationCadaverine010405 organic chemistryChemistryLight activatedLight irradiationGeneral Chemistryphotochromism0104 chemical sciencesdiarylethenes540 Chemie und zugeordnete Wissenschaftenamineddc:540diaryletheneAmine gas treatingAngewandte Chemie International Edition
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Proton‐Gated Ring‐Closure of a Negative Photochromic Azulene‐Based Diarylethene

2020

Abstract 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. Conventionally, their acidic/basic sites are on hetero‐atoms, which are orthogonal to the photo‐active π‐center. Here, we incorporate azulene, an acid‐sensitive pure hydrocarbon, into the skeleton of a diarylethene‐type photoswitch. The latter exhibits a novel proton‐gated negative photochromic ring‐closure and its optical response upon protonation in both open and closed forms is much more pronounced than those of diarylethene photoswitches with hetero‐atom based acidic/basic moieties. …

azulenenegative photochromismProtonation010402 general chemistryPhotochemistry01 natural sciencesCatalysischemistry.chemical_compoundPhotochromismDeprotonationDiaryletheneMoleculeMolecular switchphotochemistryPhotoswitch010405 organic chemistryCommunicationPhotoswitchesGeneral ChemistryAzuleneCommunications3. Good health0104 chemical sciences540 Chemie und zugeordnete Wissenschaftenchemistryacid-base equilibriaddc:540diarylethene
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Synthesis and magnetic properties of an iron 1,2-bisthienyl perfluorocyclopentene photochromic coordination compound

2011

Abstract The coordination compound Fe(BM-4-PTP) 2 (NCS) 2 ⋅2MeOH ( 1 ) including the photoisomerizable ligand BM-4-PTP (1,2-bis(2′-methyl-5′-(pyrid-4″-yl)thien-3′-yl)perfluorocyclopentene) was obtained as an orange powder. The powder turns blue upon photocyclization of the 1,2-bisthienyl photochromic ligand induced by UV light irradiation at room temperature. Photocycloreversion is obtained by visible light irradiation of the material in the solid state. The orange and blue powders were investigated over the temperature range (5–293 K) and pressure range (1 bar–12 kbar) by magnetic susceptibility measurements and variable temperature 57 Fe Mossbauer spectroscopy. The photo-induced colour ch…

chemistry.chemical_classificationOrganic ChemistryAtmospheric temperature rangePhotochemistryPhotomagnetismMagnetic susceptibilityAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsCoordination complexInorganic ChemistryPressure rangePhotochromismchemistry.chemical_compoundchemistryDiaryletheneMössbauer spectroscopyElectrical and Electronic EngineeringPhysical and Theoretical ChemistrySpectroscopyOptical Materials
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