Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Hybridization of Atomic Orbitals I03:24

Hybridization of Atomic Orbitals I

46.5K
The mathematical expression known as the wave function, ψ, contains information about each orbital and the wavelike properties of electrons in an isolated atom. When atoms are bound together in a molecule, the wave functions combine to produce new mathematical descriptions that have different shapes. This process of combining the wave functions for atomic orbitals is called hybridization and is mathematically accomplished by the linear combination of atomic orbitals. The new orbitals that...
46.5K
Hydroboration-Oxidation of Alkenes03:08

Hydroboration-Oxidation of Alkenes

7.9K
In addition to the oxymercuration–demercuration method, which converts the alkenes to alcohols with Markovnikov orientation, a complementary hydroboration-oxidation method yields the anti-Markovnikov product. The hydroboration reaction, discovered in 1959 by H.C. Brown, involves the addition of a B–H bond of borane to an alkene giving an organoborane intermediate. The oxidation of this intermediate with basic hydrogen peroxide forms an alcohol.
7.9K
Exceptions to the Octet Rule02:55

Exceptions to the Octet Rule

27.6K
Many covalent molecules have central atoms that do not have eight electrons in their Lewis structures. These molecules fall into three categories:
27.6K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Regulatory insights underlying apple to cold stress.

Horticulture research·2026
Same author

Chito-oligosaccharide loaded with ACC (1-aminocyclopropane-1-carboxylate) deaminase-producing bacteria improved soil microecology and cotton growth in salinized lands.

BMC plant biology·2026
Same author

Inside-Outside ROS Therapeutic Strategy Based on Piezoelectric Nano-Urchin for Drug-Resistant Bacteria Biofilm Infections.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026
Same author

Microbiome and metabolomics analysis of different bryophytes under cadmium stress.

BMC plant biology·2026
Same author

Multiresponsive and Tunable Circularly Polarized Luminescence in Aggregation-Induced Emission Static Helical Supramolecular Polyisocyanides.

Journal of the American Chemical Society·2026
Same author

Substituent-Engineered Spirofluorene-Boron Emitters: Integrating TADF, Visible Afterglow, and Mechanochromism in a Single Material.

ACS applied materials & interfaces·2025

Related Experiment Video

Updated: Jun 6, 2025

A Standard and Reliable Method to Fabricate Two-Dimensional Nanoelectronics
07:12

A Standard and Reliable Method to Fabricate Two-Dimensional Nanoelectronics

Published on: August 28, 2018

9.5K

Boron-Containing Organic Two Dimensional Materials: Synthesis and Application.

Fenggui Zhao1,2, Mengjie An1, Nan Wang1

  • 1Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, 102488, P. R. China.

Chemistry (Weinheim an Der Bergstrasse, Germany)
|November 22, 2024
PubMed
Summary

Boron-containing organic two-dimensional materials offer unique electronic properties for diverse applications. This review summarizes their preparation and properties, highlighting their potential in optoelectronics and chemical sensing.

Keywords:
Boron-doped 2-D material;boron-doped graphene nanoribbonsboron-doped 2-D conjugated polymersboron-doped COFboron-doped graphdiyne

More Related Videos

Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions
08:56

Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions

Published on: November 30, 2022

2.7K
Exfoliation and Analysis of Large-area, Air-Sensitive Two-Dimensional Materials
10:18

Exfoliation and Analysis of Large-area, Air-Sensitive Two-Dimensional Materials

Published on: January 5, 2019

11.5K

Related Experiment Videos

Last Updated: Jun 6, 2025

A Standard and Reliable Method to Fabricate Two-Dimensional Nanoelectronics
07:12

A Standard and Reliable Method to Fabricate Two-Dimensional Nanoelectronics

Published on: August 28, 2018

9.5K
Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions
08:56

Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions

Published on: November 30, 2022

2.7K
Exfoliation and Analysis of Large-area, Air-Sensitive Two-Dimensional Materials
10:18

Exfoliation and Analysis of Large-area, Air-Sensitive Two-Dimensional Materials

Published on: January 5, 2019

11.5K

Area of Science:

  • Materials Science
  • Organic Chemistry
  • Nanotechnology

Background:

  • Organic two-dimensional (2D) materials are recognized for their defined structures and electronic properties, enabling broad applications.
  • Atomic-level structural modification is key to optimizing these materials.
  • Incorporating heteroatoms, like boron, significantly alters electronic structure and imparts novel characteristics.

Purpose of the Study:

  • To review the preparation methods and property studies of boron-containing organic 2D materials.
  • To explore the potential of these materials in optoelectronics and chemical sensing.
  • To provide a comprehensive overview of recent advancements in this field.

Main Methods:

  • Literature review focusing on synthesis and characterization techniques.
  • Analysis of structure-property relationships in boron-modified organic 2D materials.
  • Compilation of data on optoelectronic and chemical sensing performance.

Main Results:

  • Boron's electron-deficient nature enhances luminescence, semiconductor, and sensing capabilities.
  • Boron-containing organic 2D materials exhibit promising optoelectronic and chemical activity.
  • Specific examples of three types of boron-containing organic 2D materials are detailed.

Conclusions:

  • Boron-containing organic 2D materials represent a promising new class with tunable properties.
  • Their unique electronic structures facilitate advanced applications in sensing and optoelectronics.
  • Further research into their preparation and application is warranted.