Results 141 to 150 of about 85,160 (331)

fullerenes

open access: yes, 2014
Citation: 'fullerenes' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.F02547 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
openaire   +1 more source

Quantum-Chemical Study of Acceptor Properties of Fullerene and Its Bridge Derivatives [PDF]

open access: diamond, 2018
O. L. Pavlenko   +47 more
openalex   +1 more source

Photoinduced Electron Transfer (PET) as Key to Accelerate the Cycloreversion Reaction of Arylquadricyclanes

open access: yesChemistry – A European Journal, EarlyView.
It is demonstrated that the photoinduced cycloreversion of a methoxynaphthylquadricyclane in the presence of suitable photocatalysts gives quantitatively the corresponding norbornadiene. As this photochromic norbornadiene‐quadricyclane cycle has favorable properties for light energy conversion, this method provides a useful tool for the targeted ...
Julian Felix Maria Hebborn   +4 more
wiley   +1 more source

Probing Radical‐Induced Magnetic Moment Modulation at Cobalt Interfaces via Soft X‐Ray Photoelectron Spectroscopy

open access: yesChemistry – A European Journal, EarlyView.
X‐ray photoelectron spectroscopy reveals to be a powerful technique to explore subtle changes of the electronic structure at the radical/cobalt interface. The radical chemisorption influences the cobalt electronic structure and consequently its magnetic properties.
Maria Benedetta Casu
wiley   +1 more source

Biomedical Application of Fullerenes [PDF]

open access: bronze, 2013
Chunying Shu   +3 more
openalex   +1 more source

Mimicking The Photosynthetic Special Pair With Aluminum(III) Porphyrin Homodimer – Fullerene (C60) Supramolecular Assemblies Capable of Long‐Lived Charge Separation

open access: yesChemistry – A European Journal, EarlyView.
The axial‐bonding of aluminum(III) porphyrins was used to create two covalently linked special‐pair mimics to probe charge‐transfer between a porphyrin dimer and a C60 unit for artificial photosynthesis. Although excitonic coupling between the porphyrins is weak, incorporation of a second porphyrin markedly increases both the yield and lifetime of the ...
Stefan Charon   +7 more
wiley   +1 more source

Three‐Step Synthesis Toward Fluorene‐Based Non‐Fused‐Ring Acceptors for Organic Solar Cells

open access: yesChemistry – A European Journal, EarlyView.
Applying a simple three step synthesis strategy leads to two fluorene‐based non‐fused‐ring electron acceptors, FHM‐Cl and FHM‐F for organic solar cells. The chlorinated variant delivers markedly higher efficiency due to broader light harvesting and favorable molecular packing, resulting in improved charge transport and reduced recombination losses ...
Virginia Lafranconi   +10 more
wiley   +1 more source

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