Dispersion forces play a role in (Me2IPr)Fe(![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif)
NAd)R2 (Ad = adamantyl; R = neoPe, 1-nor) insertions and Fe–R bond dissociation enthalpies (BDEs)†‡
Abstract
The effects of dispersion on migratory insertion reactions and related iron–carbon bond dissociation energies pertaining to (Me2IPr)FeR2 (R = neoPe, 1-nor), and the conversion of (Me2IPr)Fe(NAd)R2 to (Me2IPr)Fe{N(Ad}R)R are investigated via calculations and structural comparisons. Dispersion appears to be an underappreciated, major contributor to common structure and reactivity relationships.
![Graphical abstract: Dispersion forces play a role in (Me2IPr)Fe( [[double bond, length as m-dash]] NAd)R2 (Ad = adamantyl; R = neoPe, 1-nor) insertions and Fe–R bond dissociation enthalpies (BDEs)](/aa/Image/Get?imageInfo.ImageType=GA&imageInfo.ImageIdentifier.ManuscriptID=C7DT04145D&imageInfo.ImageIdentifier.Year=2018)
- This article is part of the themed collection: Philip Power at 65: an icon of organometallic chemistry
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![[double bond, length as m-dash]](https://www.rsc.org/images/entities/h2_char_e001.gif)
NAd)R2 (Ad = adamantyl; R = neoPe, 1-nor) insertions and Fe–R bond dissociation enthalpies (BDEs)
