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Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

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Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
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Metal-Ligand Bonds02:51

Metal-Ligand Bonds

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The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
19.3K
Chirality at Nitrogen, Phosphorus, and Sulfur02:30

Chirality at Nitrogen, Phosphorus, and Sulfur

5.5K
Chirality is most prevalent in carbon-based tetrahedral compounds, but this important facet of molecular symmetry extends to sp3-hybridized nitrogen, phosphorus and sulfur centers, including trivalent molecules with lone pairs. Here, the lone pair behaves as a functional group in addition to the other three substituents to form an analogous tetrahedral center that can be chiral.
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
5.5K
Complexometric Titration: Ligands00:43

Complexometric Titration: Ligands

2.6K
Different monodentate and polydentate ligands are used as complexing agents in complexometric titration reactions. The formation of complexes by mono- and bidentate ligands involves two or more intermediate steps, limiting their use as complexing agents. In comparison, polydentate ligands can form complexes with metal ions in a single-step process, facilitating sharper end points. This means polydentate ligands, such as amino carboxylic acid derivatives, are most commonly employed in...
2.6K
Ligand Binding and Linkage00:49

Ligand Binding and Linkage

4.4K
Allosteric proteins have more than one ligand binding site; the binding of a ligand to any of these sites influences the binding of ligands to the other sites. When a protein is allosteric, its binding sites are called coupled or linked.  In the case of enzymes, the site that binds to the substrate is known as the active site and the other site is known as the regulatory site. When a ligand binds to the regulatory site, this leads to conformational changes in the protein that can influence...
4.4K
¹H NMR: Pople Notation01:09

¹H NMR: Pople Notation

2.4K
The Pople nomenclature system classifies spin systems based on the difference between their chemical shifts. Coupled spins are denoted by capital letters with subscripts indicating the number of equivalent nuclei. When the coupled nuclei have well-separated chemical shifts, they are assigned letters that are far apart in the alphabet, such as A and X. When the difference in chemical shifts is small, coupled nuclei are named using adjacent letters of the alphabet (AB, MN, or XY).
A proton...
2.4K

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Updated: May 5, 2026

Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
12:08

Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes

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P,N ligands in asymmetric catalysis.

Michael P Carroll1, Patrick J Guiry

  • 1Centre for Synthesis and Chemical Biology, School of Chemistry and Chemical Biology, University College Dublin, Belfield, Dublin 4, Ireland. patrick.guiry@ucd.ie.

Chemical Society Reviews
|November 22, 2013
PubMed
Summary
This summary is machine-generated.

Phosphorus, nitrogen (P,N) ligands are crucial for asymmetric catalysis. This review highlights recent advances and novel applications of these versatile ligands in various catalytic reactions.

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Area of Science:

  • Organic chemistry
  • Catalysis
  • Ligand design

Background:

  • Phosphorus, nitrogen (P,N) ligands are a key component in modern asymmetric catalysis.
  • Their unique electronic and steric properties enable high selectivity and reactivity.

Purpose of the Study:

  • To provide an updated overview of recent applications of P,N ligands in asymmetric catalysis.
  • To focus on emerging classes of P,N ligands and their use in novel catalytic transformations.
  • To highlight the versatility of established P,N ligands in new reaction methodologies.

Main Methods:

  • Literature review of recent research in asymmetric catalysis involving P,N ligands.
  • Analysis of the scope and limitations of newly developed P,N ligand systems.
  • Examination of the application of established P,N ligands in previously unexplored reactions.

Main Results:

  • Demonstration of the expanding utility of P,N ligands across a diverse range of asymmetric reactions.
  • Introduction of novel P,N ligand architectures with enhanced catalytic performance.
  • Successful application of established P,N ligands in new synthetic methodologies, broadening their scope.

Conclusions:

  • P,N ligands continue to be a rapidly evolving and highly effective class of ligands for asymmetric catalysis.
  • Recent developments underscore the potential for designing new P,N ligands and expanding the application scope of existing ones.
  • These ligands are indispensable tools for achieving high enantioselectivity in complex chemical synthesis.