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Enantiotopic groups are identical and indistinguishable except in chiral environments. For instance, the CH 2 hydrogens in ethanol (CH 3 CH 2 OH) are normally enantiotopic, but can be made different (diastereotopic) if combined with a chiral center, for instance by conversion to an ester of a chiral carboxylic acid such as lactic acid, or if coordinated to a chiral metal center, or if ...
In the context of nuclear magnetic resonance (NMR), the term magnetic inequivalence refers to the distinction between magnetically active nuclear spins by their NMR signals, owing to a difference in either chemical shift (magnetic inequivalence by the chemical shift criterion) or spin–spin coupling (magnetic inequivalence by the coupling criterion).
When one face of a molecule is shielded by substituents or geometric constraints compared to the other face the faces are called diastereotopic. The same rules that determine the stereochemistry of a stereocenter (R or S) also apply when assigning the face of a molecular group. The faces are then called the Re-face and Si-face.
In stereochemistry, diastereomers (sometimes called diastereoisomers) are a type of stereoisomer. [1] Diastereomers are defined as non-mirror image, non-identical stereoisomers.
Diastereotopic methylene protons in complexes of diethyl sulfide. Thioether complexes feature pyramidal sulfur centers. Typical C-S-C angles are near 99° in both free thioethers and their complexes. The C-S distance in dimethylsulfide is 1.81 Å, which is also unaffected in its complexes. [5]
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Structure of Cp′Fe(PPh 3)(CO)I, with labels for the four diastereotopic ring protons. Deprotonation of methylcyclopentadiene gives the aromatic methylcyclopentadienyl anion. [2] This ion is useful as a ligand for organometallic complexes.
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