Nanoparticles under the light: click functionalization by photochemical thiol-yne reaction, towards double click functionalization.
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Soft fluorescent nanomaterials for biological and biomedical imagingChemically engineered persistent luminescence nanoprobes for bioimaging"Click" reactions: a versatile toolbox for the synthesis of peptide-conjugates.Tetrazine Click Chemistry for the Modification of 1-Hydroxy-1,1-methylenebisphosphonic Acids: Towards Bio-orthogonal Functionalization of Gold Nanoparticles.Versatile “click” synthesis of 1-hydroxy-1,1-methylenebisphosphonic acids with thioalkoxy substituents for the preparation of stable gold nanoparticlesImmobilized Pd on magnetic nanoparticles bearing proline as a highly efficient and retrievable Suzuki–Miyaura catalyst in aqueous mediaMagnetic nano-organocatalysts: impact of surface functionalization on catalytic activityCatechol versus bisphosphonate ligand exchange at the surface of iron oxide nanoparticles: towards multi-functionalizationOne pot microwave assisted synthesis of bisphosphonate alkene capped gold nanoparticles
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P2860
Nanoparticles under the light: click functionalization by photochemical thiol-yne reaction, towards double click functionalization.
description
2013 nî lūn-bûn
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name
Nanoparticles under the light: ...... ouble click functionalization.
@en
Nanoparticles under the light: ...... ouble click functionalization.
@nl
type
label
Nanoparticles under the light: ...... ouble click functionalization.
@en
Nanoparticles under the light: ...... ouble click functionalization.
@nl
prefLabel
Nanoparticles under the light: ...... ouble click functionalization.
@en
Nanoparticles under the light: ...... ouble click functionalization.
@nl
P2860
P50
P356
P1476
Nanoparticles under the light: ...... double click functionalization
@en
P2093
Emilie Nehlig
Paul Demay-Drouhard
P2860
P304
P356
10.1002/CHEM.201300903
P407
P577
2013-06-06T00:00:00Z