Facile covalent functionalization of boron nitride nanotubes via coupling reaction
Thang Quoc Huynh1,2, Minsung Kang1, Jeung Gon Kim2,3
1Institute of Advanced Composite Materials, Korea Institute of Science and Technology (KIST) Chudong-ro 92, Bongdong-eup Wanju-gun 55324 Jeonbuk Korea ahn75@kist.re.kr.
Abstract:
A broad range of functionalized boron nitride nanotubes has been synthesized using a facile method based on the coupling reaction between BNNT and arenediazonium tetrafluoroborate derivatives. The formation of covalent bonds between nanotubes and organic moieties results in homogeneous dispersions in organic solvents, such as N,N'-dimethylformamide, acetone, isopropanol, and tetrahydrofuran. Digital images demonstrated improved and stabilized dispersions lasting for several days, while TEM analysis indicated no breakdown of nanotubes due to the mild reaction conditions employed. The functionalization process was further confirmed through additional characterization, employing FTIR, XPS, and TGA. Surface-functionalized materials exhibited a significant weight percentage of functionality, reaching up to 21.8% according to TGA.
More Related Videos
08:56Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions
Published on: November 30, 2022
08:40Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
Published on: December 6, 2021
Related Concept Videos
Hydroboration-Oxidation of Alkenes
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
Exceptions to the Octet Rule
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Hybridization of Atomic Orbitals I
