A new synthetic approach for the production of carbon nanomaterials (CNM) decorated with organophosphorus moieties is presented. Three different triphenylphosphine oxide (TPPO) derivatives were used to decorate oxidized multiwalled carbon nanotubes (ox-MWCNTs) and graphene platelets (GPs). The TPPOs chosen bear functional groups able to react with the CNMs by Tour reaction (an amino group), nitrene cycloaddition (an azido group) or CuAAC reaction (one terminal C-C triple bond). All the adducts were characterized by FTIR, Raman spectroscopy, TEM, XPS, elemental analysis and ICP-AES. The cycloaddition of nitrene provided the higher loading on ox-MWCNTs and GPs as well, while the Tour approach gave best results with nanotubes (CNTs). Finally, we investigated the possibility to reduce the TPPO functionalized CNMs to the corresponding phosphine derivatives and applied one of the materials produced as heterogeneous organocatalyst in a Staudinger ligation reaction.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331327PMC
http://dx.doi.org/10.3762/bjnano.8.52DOI Listing

Publication Analysis

Top Keywords

decorated organophosphorus
8
organophosphorus moieties
8
nanostructured carbon
4
carbon materials
4
materials decorated
4
moieties synthesis
4
synthesis application
4
application synthetic
4
synthetic approach
4
approach production
4

Similar Publications

Ru-OH-Zr Site over Metal-Organic Frameworks Boosts Coreactant Activation for Efficient Electrochemiluminescence.

Nano Lett

January 2025

State Key Laboratory of Green Pesticide, International Joint Research Center for Intelligent Biosensing Technology and Health, College of Chemistry, Central China Normal University, Wuhan 430079, P.R. China.

Metal-organic frameworks (MOFs) are promising electrochemiluminescent (ECL) nanoemitters. Great endeavors have been made to optimize the inherent luminescent properties, yet most MOFs suffer from poor coreactant activation ability, resulting in limited ECL. Therefore, it is urgent to integrate and design efficient catalytic centers within MOFs.

View Article and Find Full Text PDF

Food safety is an important issue to protect humane health and improve the life quality. Hence, analysis of the possible contaminants in food samples is essential. A rapid and efficient vortexed-assisted dispersive µ-solid-phase extraction coupled with gas chromatography-mass spectrometry was proposed for simultaneous separation/preconcentration and determination of five commonly used organophosphorus pesticides.

View Article and Find Full Text PDF

Background: Overcoming radio-resistance and enhance radio-sensitivity to obtain desired therapeutic outcome plays an important role in treating cancer.

Methods: Here we constructed a versatile enzyme-like nano-radiosensitizer MDP. MDP is composed of MnCO decorated and Ru-based nanozyme with triphenylphosphine (TPP) group coordinated on the surface.

View Article and Find Full Text PDF

Precisely detecting organophosphorus pesticides (OPs) is paramount in upholding human safety and environmental preservation, especially in food safety. Herein, an electrochemical acetylcholinesterase (AChE) sensing platform entrapped in chitosan (Chit) on the glassy carbon electrodes (GCEs) decorated with Pt/MoS/TiC MXene (Pt/MoS/TM) was constructed for the detection of chlorpyrifos. It is worth noting that Pt/MoS/TM possesses good biocompatibility, remarkable electrical conductivity, environmental stability and large specific surface area.

View Article and Find Full Text PDF

Green-fluorescent biocompatible carbon dots with a quantum yield of 40% were successfully synthesized through a solvothermal process and then they are comprehensively characterized. The carbon dots showed a negatively charged surface owing to the presence of carboxylic groups. This negative surface charge hinders the effective targeting and imaging of mitochondria.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!