Search results for "Covalent bond"
showing 10 items of 305 documents
Gas Selective Ultrathin Organic Covalent Networks Synthesized by iPECVD: Does the Central Metal Ion Matter?
2017
The potential of porphyrin-derived metal organic covalent networks (OCN) thin films on light gas separations has been recently demonstrated. However, whether or not the central metal ion of the porphyrin plays a key role on separation performance has yet to be elucidated. Here, one metal-free and three metal-containing (zinc(II), manganese(III), and cobalt(II)) porphyrin-derived OCN thin films are successfully deposited on various substrates via an easily scalable initiated plasma-enhanced chemical vapor deposition approach. Among these four porphyrin-derived OCN thin films exhibiting superior light gas separation performances, three of them are synthesized for the first time. The gas perme…
Supported C60-IL-PdNPs as extremely active nanocatalysts for C-C cross-coupling reactions
2016
A C60-ionic liquid hybrid has been covalently linked to three different solid supports, namely amorphous silica, SBA-15 and Fe2O3@SiO2, and the resulting materials have been employed as covalently supported ionic liquid phases (cSILP) in order to immobilize and stabilize palladium nanoparticles (PdNPs). These novel hybrid materials are based on a sort of "matryoshka" system (PdNPs@imidazolium-salt@C60@support) in which the imidazolium-based moieties have not been directly linked to the surface of the support, but they are present in an octopus-like spatial arrangement on the uniformly surface-distributed fullerenes. These materials have been fully characterized and successfully employed as …
Dibenzoquinquethiophene- and Dibenzosexithiophene-Based Hole-Transporting Materials for Perovskite Solar Cells
2018
Fused oligothiophene-based π-conjugated organic derivatives have been widely used in electronic devices. In particular, two-dimensional (2D) heteroarenes offer the possibility of broadening the scope by extending the π-conjugated framework, which endows enhanced charge transport properties due to the potential intermolecular π–π stacking. Here, the synthesis and characterization of two new small-molecule hole-transporting materials (HTMs) for perovskite solar cells (PSCs) are reported. The newly custom-made compounds are based on dibenzoquinquethiophene (DBQT) and dibenzosexithiophene (DBST) cores, which are covalently linked to triphenylamine moieties to successfully afford the four-armed …
Microwave-Assisted Synthesis of Covalent OrganicFrameworks: A Review
2020
[EN] Covalent organic frameworks (COFs) are relatively recent materials. They have received great attention due to their interesting properties. However, the application of microwaves in their synthesis, despite its advantages such as faster and more reproducible processes, is a minority. Herein, a comprehensive compilation of the research results published in the microwave-assisted synthesis (MAS) of COFs is presented. This review includes articles of 2D and 3D COFs prepared using microwaves as source of energy. The articles have been classified depending on the functional groups including boronate ester, imines, enamines, azines, and triazines, among others. It compiles the main parameter…
Synthesis of a fluorinated graphene oxide-silica nanohybrid: Improving oxygen affinity
2016
An easy method to achieve a fluorinated graphene oxide–silica nanohybrid (GOSF) is presented. Graphene oxide (GO) was synthesized by Hummer's modified method, the GO–silica nanohybrid (GOS) was obtained via Fischer esterification, the fluorinated moiety (3-pentadecafluoroheptyl-5-perfluorophenyl-1,2,4-oxadiazole) was introduced by nucleophilic substitution operated by the hydroxyl functionalities onto the GOS surface. Full characterization of the new materials confirmed the formation of covalent bonds between the graphene oxide/silica hybrid matrix and the fluorinated moieties. The proposed methodology offers an easy way to get fluorinated carbon/silica hybrid nanomaterials avoiding the har…
Synthesis and characterization of nanomaterial based on halloysite and hectorite clay minerals covalently bridged
2021
Halloysite is an aluminosilicate clay with a predominantly hollow tubular structure (HNTs) able to act as a nanocontainer for the encapsulation of several chemicals. However, HNTs possess low affinity for metal ions in their pristine form and they need to be modified for improving their adsorption capabilities. Therefore, to overcome this issue herein we report a straightforward approach for the covalent modification of the external surface of halloysite nanotubes with hectorite clay. Compared to halloysite, hectorite possesses a lamellar structure with higher cation exchange capacity. The covalent linkage between the two clays was verified by several techniques (FTIR spectroscopy, 13C CP-M…
Functionalisation of MoS2 2D layers with diarylethene molecules
2021
Functionalisation of two dimensional (2D) materials with stimuli-responsive molecules has been scarcely investigated. Here, MoS2 layers obtained by chemical exfoliation are covalently and non-covalently functionalised using two photoswitchable diarylethene derivatives under their open- and closed-ring isomers. The choice of these light-responsive molecules is based on their excellent thermal irreversibility and fatigue resistance. The characterisation of the resultant molecular/2D heterostructures proves the successful anchoring of the molecules by both approaches as well as the influence that the driving interaction has in the photoswitching behaviour of the diarylethene isomers after thei…
Aluminum-lithium clusters: First-principles simulation of geometries and electronic properties
2002
The geometries and electronic properties of small lithium-rich ${\mathrm{Al}}_{N}{\mathrm{Li}}_{5N}$ $(N=1--6,10)$ clusters are studied using first-principles simulations. Aluminum ions form a compact inner core configuration in the clusters that changes into a chainlike skeleton embedded in a lithium surrounding as the cluster size increases. This behavior restricts $s\ensuremath{-}p$ hybridization effects and causes separate s and p bands in the electronic energy spectrum. A significant charge transfer from Li ions and nearby Al ions strengthens ionic Al-Li bonds, while Al-Al bonds gain a more covalent nature. The evolution of some bulk properties of $B2$ and $B32$ phases of AlLi alloys i…
Tunability by alkali metal cations of photoinduced charge separation in azacrown functionalized graphene.
2013
A modified graphene oxide containing aza-9-crown-3 ether units covalently anchored has been prepared; aqueous suspensions of this material in the presence of Li(+), Na(+) and K(+) cations exhibit enhanced electrochemical response, enhanced photoinduced charge separation and longer lifetimes, facts that can be attributed to stabilization of electrons on graphene oxide by the nearby alkali metal cation-azacrown complexes.
Influence of the covalent grafting of organic radicals to graphene on its magnetoresistance
2013
Graphene was obtained by direct exfoliation of graphite in o-dichlorobenzene (oDCB) or benzylamine, and further functionalized with 4,4′-[(1,3-dioxo-1,3-propanediyl)bis(oxy)]bis[2,2,6,6-tetramethyl-1-piperidinyloxy] (1-TEMPO) organic radicals by using the Bingel–Hirsch cyclopropanation reaction. Here, the use of different solvents permits variation of the density of radicals anchored to the carbon layers. Covalent grafting is unambiguously demonstrated by TGA, μ-Raman, XPS and EPR measurements, which also rule out spurious physisorption. Our transport measurements indicate that the conduction mechanism varies as a function of the density of radicals grafted to the carbon layers. Moreover, t…