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Hybridization of Atomic Orbitals I03:24

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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...
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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.
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Borophene: Synthesis, Chemistry, and Electronic Properties.

Kai Wang1, Shilpa Choyal1, Jeremy F Schultz2

  • 1Department of Chemistry, University of Illinois Chicago, Chicago, IL 60607, USA.

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PubMed
Summary

Two-dimensional boron sheets, or borophene, exhibit unique structures and properties. This review summarizes experimental findings on borophene synthesis, chemistry, and electronic properties, highlighting challenges for applications.

Keywords:
2D materialsBoropheneNanostructuresSubstrate-supported growthSurface chemistry

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Area of Science:

  • Materials Science
  • Condensed Matter Physics
  • Chemistry

Background:

  • Boron, a neighbor to carbon, shows diverse structural and electronic properties.
  • Two-dimensional (2D) boron sheets (borophene) were experimentally realized in 2015.
  • Research interest in borophene's characteristics has grown significantly.

Purpose of the Study:

  • To review the experimental synthesis and properties of borophene.
  • To discuss advancements in borophene realization and its variations.
  • To provide an outlook on borophene's practical applications.

Main Methods:

  • Experimental synthesis of borophene on various substrates.
  • Characterization of borophene, borophane, and bilayer borophene.
  • Review of chemical modifications and heterostructure integration.

Main Results:

  • Borophene synthesis on diverse substrates yields unique phases and properties.
  • Borophene undergoes oxidation and hydrogenation, and can form heterostructures.
  • Electronic properties of borophene have been investigated.

Conclusions:

  • Borophene exhibits promising properties for various applications.
  • Challenges remain in realizing practical applications of borophene.
  • Further research is needed to overcome limitations and explore solutions.