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Preparation of Nitriles01:12

Preparation of Nitriles

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One of the common methods to prepare nitriles is the dehydration of amides. This method requires strong dehydrating agents like phosphorous pentoxide or boiling acetic anhydride for converting amides to nitriles. Another reagent namely, thionyl chloride also accomplishes the dehydration of amides, where amide acts as a nucleophile. The first step of the mechanism involves the nucleophilic attack by the amide on the thionyl chloride to form an intermediate. In the next step, the electron pairs...
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Electrophilic Aromatic Substitution: Nitration of Benzene01:20

Electrophilic Aromatic Substitution: Nitration of Benzene

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The nitration of benzene is an example of an electrophilic aromatic substitution reaction. It involves the formation of a very powerful electrophile, the nitronium ion, which is linear in shape. The reaction occurs through the interaction of two strong acids, sulfuric and nitric acid.
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Catalysis02:50

Catalysis

30.1K
The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
30.1K
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride01:26

Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride

2.2K
Radical substitution reactions can be used to remove functional groups from molecules. The hydrogenolysis of alkyl halides is one such reaction, where the weak Sn–H bond in tributyltin hydride reacts with alkyl halides to form alkanes. Here, the reagent Bu3SnH yields tributyltin halide as a byproduct.
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
2.2K
Preparation of 1° Amines: Gabriel Synthesis01:28

Preparation of 1° Amines: Gabriel Synthesis

4.5K
Direct alkylation is not a suitable method for synthesizing amines because it produces polyalkylated products. Gabriel synthesis is the most preferred method to exclusively make primary amines. The method uses phthalimide, which contains a protected form of nitrogen that participates in alkylation only once to predominantly give primary amines.
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
4.5K
2° Amines to N-Nitrosamines: Reaction with NaNO201:20

2° Amines to N-Nitrosamines: Reaction with NaNO2

5.4K
Secondary amines react with nitrous acid to form N-nitrosamines, as depicted in Figure 1. Nitrous acid, a weak and unstable acid, is formed in situ from an aqueous solution of sodium nitrite and strong acids, such as hydrochloric acid or sulfuric acid, in cold conditions. In the presence of an acid, the nitrous acid gets protonated. The subsequent loss of water results in the formation of the electrophile known as nitrosonium ion.
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Novel Precursor for h‑BN Synthesis on Ni(111) Substrates.

Sergi Campos-Jara1, Tycho Roorda1, Laurens P M de Jong1

  • 1Leiden Insitute of Chemistry, Leiden University, Einsteinweg 55, Leiden 2333 CC, Netherlands.

The Journal of Physical Chemistry. C, Nanomaterials and Interfaces
|September 10, 2025
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Researchers synthesized high-quality single-crystalline hexagonal boron nitride (h-BN) using hexamethylborazine (HMB) on nickel substrates. This novel method advances h-BN growth mechanisms for next-generation materials.

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Area of Science:

  • Materials Science
  • Surface Science
  • Nanotechnology

Background:

  • Hexagonal boron nitride (h-BN) is a crucial material for next-generation electronics and photonics.
  • Efficient synthesis of high-quality, single-crystalline h-BN on conductive substrates remains a challenge.
  • Traditional precursors often lead to polycrystalline or defective h-BN layers.

Purpose of the Study:

  • To report the synthesis of single-crystalline h-BN on Ni(111) using a nonclassical precursor.
  • To investigate the role of hexamethylborazine (HMB) in facilitating h-BN growth.
  • To evaluate the feasibility of this synthesis method on industrially relevant substrates.

Main Methods:

  • Synthesis of h-BN under ultrahigh vacuum (UHV) conditions using hexamethylborazine (HMB) on Ni(111) single crystals and thin films.
  • Characterization using scanning tunneling microscopy (STM), low-energy electron microscopy (LEEM), low-energy electron diffraction (LEED), X-ray photoelectron spectroscopy (XPS), and photoemission electron microscopy (PEEM).

Main Results:

  • Successful synthesis of high-quality, single-crystalline h-BN layers on Ni(111).
  • HMB precursor facilitated methyl group diffusion into Ni(111), crucial for high-quality growth.
  • Confirmation of h-BN presence and crystallinity across the Ni(111) surface using various advanced techniques.

Conclusions:

  • The use of HMB offers a novel and effective route for synthesizing single-crystalline h-BN on metal substrates.
  • This method demonstrates potential for scalable production on industrially relevant Ni films.
  • The study advances the fundamental understanding of h-BN growth mechanisms, paving the way for improved synthesis strategies.