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Bond stretch isomer information


In chemistry, bond stretch isomerism is a concept of isomerism based on variations of bond length. The concept was proposed in the 1970s but was refuted in the 1990s.[1]

The phenomenon was first invoked to explain the observation of blue and green isomers of mer-MoOCl2(PMe2Ph)3, where PMe2Ph is dimethylphenylphosphine. These isomers were shown, purportedly, by X-ray crystallography to differ with respect to the length of the Mo-O bond, which differed by 0.2 Å. Subsequent work showed that the supposed green bond stretch isomer consisted of blue mer-MoOCl2(PMe2Ph)3 contaminated with a small amount of yellow mer-MoCl3(PMe2Ph)3. The nearly isomorphous replacement of Mo-O unit with small amounts of Mo-Cl unit results in artifactually long Mo-O distance in the green sample. In essence the deception arises because the crystallographic disorder was not modeled appropriately. Several such examples were uncovered.

  1. ^ Parkin, G., "Bond-Stretch Isomerism in Transition Metal Complexes: a Reevaluation of Crystallographic Data", Chem. Rev. 1993, volume 93, 887-911. doi:10.1021/cr00019a003

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Bond stretch isomer

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constitutional isomer See structural isomer. convection cooling curve coordinate chemistry coordinate covalent bond See dipolar bond. coordination complex...

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shows an infrared vibrational frequency of 1220 cm−1 due to the stretching of the bond. The free radical nature of PO makes it highly reactive and unstable...

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doubly bridging CO ligands, denoted μ2-CO or often just μ-CO, the bond stretching frequency νCO is usually shifted by 100–200 cm−1 to lower energy compared...

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been prepared. The molecules are linear. In ArAuCl the Ar−Au bond is 2.47 Å, the stretching frequency is 198 cm−1 and the dissociation energy is 47 kJ/mol...

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as cis and trans isomers. The C=N bonds, which are near 129 picometers in length, are shorter than C-N single bonds. Cis/trans isomers are observed. The...

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