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Related Concept Videos

Ion Exchange01:17

Ion Exchange

635
Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or...
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Ionic Bonds00:42

Ionic Bonds

119.5K
Overview
When atoms gain or lose electrons to achieve a more stable electron configuration they form ions. Ionic bonds are electrostatic attractions between ions with opposite charges. Ionic compounds are rigid and brittle when solid and may dissociate into their constituent ions in water. Covalent compounds, by contrast, remain intact unless a chemical reaction breaks them.
Opposing Charges Hold Ions Together in Ionic Compounds
Ionic bonds are reversible electrostatic interactions between ions...
119.5K
Thermal Electrocyclic Reactions: Stereochemistry01:17

Thermal Electrocyclic Reactions: Stereochemistry

2.1K
The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
2.1K
α-Alkylation of Ketones via Enolate Ions01:10

α-Alkylation of Ketones via Enolate Ions

3.3K
Ketones with α protons are deprotonated by strong bases like lithium diisopropylamide (LDA) to form enolate ions. The anion is stabilized by resonance, and its hybrid structure exhibits negative charges on the carbonyl oxygen and the α carbon. This ambident nucleophile can attack an electrophile via two possible sites: the carbonyl oxygen, known as O-attack, or the α carbon, known as C-attack. The nucleophilic attack via the carbanionic site is preferred. This is due to the...
3.3K
Pericyclic Reactions: Introduction01:17

Pericyclic Reactions: Introduction

8.4K
Pericyclic reactions are organic reactions that occur via a concerted mechanism without generating any intermediates. The reactions proceed through the movement of electrons in a closed loop to form a cyclic transition state, where rearrangement of the σ and π bonds yields specific products.
Pericyclic reactions can be classified into three categories: electrocyclic reactions, cycloaddition reactions, and sigmatropic rearrangements. Electrocyclic reactions and sigmatropic...
8.4K
Ionic Bonding and Electron Transfer02:48

Ionic Bonding and Electron Transfer

42.0K
Ions are atoms or molecules bearing an electrical charge. A cation (a positive ion) forms when a neutral atom loses one or more electrons from its valence shell, and an anion (a negative ion) forms when a neutral atom gains one or more electrons in its valence shell. Compounds composed of ions are called ionic compounds (or salts), and their constituent ions are held together by ionic bonds: electrostatic forces of attraction between oppositely charged cations and anions. 
42.0K

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Supported Ionic Liquids and their Applications in Organic Transformations.

Ambika1, Pradeep Pratap Singh2

  • 1Department of Chemistry, Hansraj College, University of Delhi, Delhi, India.

Current Organic Synthesis
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Summary

Supported ionic liquids (SILs) offer a greener alternative to volatile organic solvents, combining heterogeneous and homogeneous catalysis benefits. These stable, reusable materials enhance various organic transformations with easy product isolation.

Keywords:
Supported ionic liquidscross-coupling reactiondesigner solventgreen catalystorganic transformationspollutants

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Area of Science:

  • Green Chemistry
  • Materials Science
  • Catalysis

Background:

  • Ionic liquids (ILs) are emerging as environmentally friendly solvents, replacing hazardous volatile organic compounds.
  • Supported ionic liquids (SILs) are gaining attention for their unique properties, synthesized by immobilizing ILs on solid supports.
  • SILs bridge the gap between heterogeneous and homogeneous catalysis, offering combined advantages.

Approach:

  • This review discusses the classification and preparation methods of SILs.
  • It explores the diverse applications of SILs in organic synthesis.
  • Focus is placed on SILs' role in reactions like cross-coupling, oxidation, reduction, and biocatalysis.

Key Points:

  • SILs exhibit enhanced stability, reusability, and recoverability compared to traditional solvents.
  • They facilitate easy product isolation and prevent IL leaching.
  • SILs demonstrate versatility in catalyzing a wide range of organic transformations.

Conclusions:

  • Supported ionic liquids represent a significant advancement in sustainable chemistry.
  • Their unique properties and broad applicability make them valuable tools for organic synthesis.
  • SILs offer a promising route towards greener and more efficient chemical processes.