Results 1 to 10 of about 179,442 (256)

The TDDFT Excitation Energies of the BODIPYs; The DFT and TDDFT Challenge Continues

open access: yesMolecules, 2021
The derivatives of 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) are pivotal ingredients for a large number of functional, stimuli-responsive materials and therapeutic molecules based on their photophysical properties, and there is a urgent need to
Adrien Schlachter   +6 more
doaj   +1 more source

Photophysical study and in vitro approach against Leishmania panamensis of dicloro-5,10,15,20-tetrakis(4-bromophenyl)porphyrinato Sn(IV) [version 3; peer review: 2 approved]

open access: yesF1000Research, 2021
Background: Photodynamic therapy activity against different biological systems has been reported for porphyrins. Porphyrin modifications through peripheral groups and/or by metal insertion inside the ring are main alternatives for the improvement of its ...
Fabián Espitia-Almeida   +5 more
doaj   +1 more source

Synthesis, electronic and photophysical properties of a bisacridinium-Zn(II) porphyrin conjugate

open access: yesComptes Rendus. Chimie, 2021
The synthesis of a novel bisacridinium-Zn(II) porphyrin is reported and its properties investigated via electrochemical, photophysical and computational studies. Cyclic voltammetry studies revealed a two-electron oxidation of the Zn(II) porphyrin and the
Edo-Osagie, Amy   +7 more
doaj   +1 more source

Spectroscopic Investigations of Porphyrin-TiO2 Nanoparticles Complexes

open access: yesMolecules, 2022
This study presents the spectral characterization of TiO2 nanoparticles (NPs) functionalized with three porphyrin derivatives: 5,10,15,20-(Tetra-4-aminophenyl) porphyrin (TAPP), 5,10,15,20-(Tetra-4-methoxyphenyl) porphyrin (TMPP), and 5,10,15,20-(Tetra-4-
Andra Dinache   +6 more
doaj   +1 more source

Porphyrin Wheels [PDF]

open access: yesJournal of the American Chemical Society, 1996
A simple method to prepare porphyrin 'wheels' on a micrometer scale is described. It is possible to arrange several types of porphyrin derivatives, including Protoporphyrin IX and Chlorophyll-a, in the form of rings using this method. A mechanism for the formation of these types of assemblies is proposed that is based on the generation of '2D-gas ...
Schenning, A.P.H.J   +4 more
openaire   +2 more sources

Synthesis and Applications of Porphyrin-Biomacromolecule Conjugates

open access: yesFrontiers in Chemistry, 2021
With potential applications in materials and especially in light-responsive biomedicine that targets cancer tissue selectively, much research has focused on developing covalent conjugation techniques to tether porphyrinoid units to various ...
Pravin Pathak   +4 more
doaj   +1 more source

Anthracene‐Porphyrin Nanoribbons

open access: yesAngewandte Chemie International Edition, 2023
Abstract π‐Conjugated nanoribbons attract interest because of their unusual electronic structures and charge‐transport behavior. Here, we report the synthesis of a series of fully edge‐fused porphyrin‐anthracene oligomeric ribbons (dimer and trimer), together with a computational study of the corresponding ...
Zhu, H   +4 more
openaire   +3 more sources

Fullerene—Porphyrin Constructs [PDF]

open access: yesChemInform, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
Boyd, Peter DW, Reed, Christopher A
openaire   +4 more sources

Electron Spin Relaxation of Photoexcited Porphyrin in Water—Glycerol Glass

open access: yesMolecules, 2020
Recently, the photoexcited triplet state of porphyrin was proposed as a promising spin-label for pulsed dipolar electron paramagnetic resonance (EPR).
Natalya Sannikova   +5 more
doaj   +1 more source

Interlocked Porphyrin Switches [PDF]

open access: yesChemistry – A European Journal, 2013
AbstractWe describe the synthesis of a series of interlocked structures from porphyrin–glycoluril cage compounds and bis(olefin)‐terminated viologens by an olefin‐metathesis protocol. The length of the chain connecting the olefin substituents with the viologen has a marked effect on the products of the ring‐closure reaction.
Coumans, R.G.E.   +5 more
openaire   +5 more sources

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