Results 21 to 30 of about 40,605 (259)

Sepiolite promotes photodegradation of pyrene under visible light

open access: yesEcotoxicology and Environmental Safety, 2023
Mechanochemistry and photocatalysis are emergent technologies for the remediation of polycyclic aromatic hydrocarbons (PAHs) in soils. In this work, mechanochemistry and photocatalysis are combined for pyrene degradation.
Gema Marcelo   +4 more
doaj   +1 more source

A study of the photocatalytic properties of chitosan-TiO2 composites for pyrene decomposition [PDF]

open access: yesНаучно-технический вестник информационных технологий, механики и оптики, 2021
In this work, nano- and microcomposites of chitosan-TiO2 were developed for the photocatalytic decomposition of pyrene, which is one of polycyclic aromatic hydrocarbons.
Danila A. Tatarinov   +2 more
doaj   +1 more source

Fate and distribution of pyrene in Ilyanassa obsoleta exposed through the diet [PDF]

open access: yesInvertebrate Survival Journal, 2010
The ability of Eastern mud snails to bioaccumulate and biotransform a model polycyclic aromatic hydrocarbon (PAH), pyrene (PY), was investigated. The contaminant was added to fish at levels ranging from 2 to 5,000 ng/animal fed 20 mg/each and fed to ...
S Erskine   +3 more
doaj   +1 more source

Unpredicted Concentration-Dependent Sensory Properties of Pyrene-Containing NBN-Doped Polycyclic Aromatic Hydrocarbons

open access: yesMolecules, 2022
Pyrene molecules containing NBN-doped polycyclic aromatic hydrocarbons (PAHs) have been synthesized by a simple and efficient intermolecular dehydration reaction between 1-pyrenylboronic acid and aromatic diamine.
Hang Xiao   +6 more
doaj   +1 more source

Li+ Selective Podand-Type Fluoroionophore Based on a Diphenyl Sulfoxide Derivative Bearing Two Pyrene Groups

open access: yesMolecules, 2011
New podand-type fluoroionophores having two pyrene moieties: 2,2´-bis(1-pyrenylacetyloxy)diphenyl sulfide (3), 2,2´-bis(1-pyrenylacetyloxy)diphenyl sulfoxide (4), and 2,2´-bis(1-pyrenylacetyloxy)diphenyl sulfone (5), have been synthesized by connecting ...
Tetsuo Takemura   +2 more
doaj   +1 more source

Dynamic exciton localisation in a pyrene–BODIPY–pyrene dye conjugate [PDF]

open access: yesPhysical Chemistry Chemical Physics, 2019
The photophysics of a molecular triad consisting of a BODIPY dye and two pyrene chromophores attached in 2-position are investigated by steady state and fs-time resolved transient absorption spectroscopy as well as by field induced surface hopping (FISH) simulations.
Nina Auerhammer   +7 more
openaire   +3 more sources

Influence of perylenediimide–pyrene supramolecular interactions on the stability of DNA-based hybrids: Importance of electrostatic complementarity

open access: yesBeilstein Journal of Organic Chemistry, 2014
Aromatic π–π stacking interactions are ubiquitous in nature, medicinal chemistry and materials sciences. They play a crucial role in the stacking of nucleobases, thus stabilising the DNA double helix.
Christian B. Winiger   +3 more
doaj   +1 more source

(4Z,5E,9E,10Z)-N4,N5,N9,N10-Tetrakis(2,6-diisopropylphenyl)pyrene-4,5,9,10-tetraimine

open access: yesIUCrData, 2016
The title molecule, C64H74N4, consists of a pyrene backbone with imine moieties located on the 4-, 5-, 9-, and 10-positions of the ring system. The aryl groups on these imines are sterically bulky 2,6-diisopropylphenyl units.
Owen M. Williams, Alan H. Cowley
doaj   +1 more source

Strong emission of excimers realized by dense packing of pyrenes in tailored bola-amphiphile nano assemblies

open access: yesCell Reports Physical Science, 2022
Summary: Pyrene is known for the quenched emission of excimers, especially in aqueous solution. Here, we report strong emission of pyrene excimers realized in amphiphile assemblies by controlling the face-to-face distance between the pyrene planes.
Yuhan Zhao   +4 more
doaj   +1 more source

1-(Hydroxymethyl)pyrene [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2010
The asymmetric unit of the title compound, C(17)H(12)O, contains two molecules, in which the fused aromatic ring systems are almost planar [maximum deviations = 0.0529 (9) and 0.0256 (9) Å]. In the crystal, aromatic π-π stacking inter-actions (perpendicular distance of centroids of about 3.4 Å) and strong O-H⋯O hydrogen bonds result in a helical ...
Tobias Gruber   +2 more
openaire   +4 more sources

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