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Related Concept Videos

Prochirality02:05

Prochirality

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The concept of prochirality leads to the nomenclature of the individual faces of a molecule and plays a crucial role in the enantioselective reaction. It is a concept where two or more achiral molecules react to produce chiral products. A typical process is the reaction of an achiral ketone to generate a chiral alcohol. Here, the achiral reactant reacts with an achiral reducing agent, sodium borohydride, to generate an equimolar mixture of the chiral enantiomers of the product. For example, an...
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Molecules with Multiple Chiral Centers02:25

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Molecules that possess multiple chiral centers can afford a large number of stereoisomers. For instance, while some molecules like 2-butanol have one chiral center, defined as a tetrahedral carbon atom with four different substituents attached, several molecules like butane-2,3-diol have multiple chiral centers. A simple formula to predict the number of stereoisomers possible for a molecule with n chiral centers is 2n. However, there can be a lower number where some of the stereoisomers are...
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Chirality02:25

Chirality

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Chirality is a term that describes the lack of mirror symmetry in an object. In other words, chiral objects cannot be superposed on their mirror images. For example, our feet are chiral, as the mirror image of the left foot, the right foot, cannot be superposed on the left foot.
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
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Stereoisomerism02:52

Stereoisomerism

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Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...
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Chirality at Nitrogen, Phosphorus, and Sulfur02:30

Chirality at Nitrogen, Phosphorus, and Sulfur

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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...
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Chirality in Nature02:30

Chirality in Nature

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Chirality is the most intriguing yet essential facet of nature, governing life’s biochemical processes and precision. It can be observed from a snail shell pattern in a macroscopic world to an amino acid, the minutest building block of life. Most of the snails around the world have right-coiled shells because of the intrinsic chirality in their genes. All the amino acids present in the human body exist in an enantiomerically pure state, except for glycine - the sole achiral amino acid.
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Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks MOFs
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Chiral metallosupramolecular architectures.

Li-Jun Chen1, Hai-Bo Yang, Mitsuhiko Shionoya

  • 1Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Department of Chemistry, East China Normal University, Shanghai 200062, P. R. China. hbyang@chem.ecnu.edu.cn.

Chemical Society Reviews
|April 29, 2017
PubMed
Summary

This review summarizes discrete chiral coordination-driven supramolecular architectures. It emphasizes recent developments in homochiral metallo-assemblies using chiral or achiral components for applications in chiral recognition and catalysis.

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Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
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Area of Science:

  • Supramolecular Chemistry
  • Coordination Chemistry
  • Chirality

Background:

  • Discrete supramolecular chirality in metallosupramolecular architectures is a growing field.
  • Coordination-driven self-assembly enables the construction of complex chiral structures.

Purpose of the Study:

  • To provide a comprehensive summary of discrete, chiral coordination-driven structures.
  • To highlight recent advancements in metallosupramolecular architectures derived from chiral components.
  • To discuss the potential applications of homochiral metallosupramolecular architectures.

Main Methods:

  • Review of existing literature on coordination-driven self-assembly.
  • Focus on chiral scaffolds (ligands) and achiral components leading to homochirality.
  • Analysis of structural diversity including helices, metallacycles, and metallocages.

Main Results:

  • Detailed overview of various discrete chiral metallosupramolecular architectures.
  • Emphasis on strategies for introducing chirality, particularly from chiral ligands or ligand twisting.
  • Exploration of homochiral assemblies using both chiral and achiral building blocks.

Conclusions:

  • Chirality in metallosupramolecular architectures can be controlled through ligand design and assembly processes.
  • Homochiral assemblies offer significant potential for advanced applications.
  • Future research directions include designing more complex architectures for enhanced functionalities.