Cyanide Ligand Assembly by Carbon Atom Transfer to an Iron Nitride
dc.contributor.author | Martinez, Jorge L. | |
dc.contributor.author | Lin, Hsiu-Jung | |
dc.contributor.author | Lee, Wei-Tsung | |
dc.contributor.author | Pink, Maren | |
dc.contributor.author | Chen, Chun Hsing | |
dc.contributor.author | Gao, Xinfeng | |
dc.contributor.author | Dickie, Diane | |
dc.contributor.author | Smith, Jeremy Michael | |
dc.date.accessioned | 2025-02-20T16:33:17Z | |
dc.date.available | 2025-02-20T16:33:17Z | |
dc.date.issued | 2017-09-21 | |
dc.description | This record is for a(n) postprint of an article published in J. Am. Chem. Soc. on 2017-09-21; the version of record is available at https://doi.org/10.1021/jacs.7b08704. | |
dc.description.abstract | The new iron(IV) nitride complex PhB($^i$Pr$_2$Im)$_3$Fe≡N reacts with 2 equiv of bis(diisopropylamino)cyclopropenylidene (BAC) to provide PhB($^i$Pr$_2$Im)$_3$Fe(CN)(N2)(BAC). This unusual example of a four-electron reaction involves carbon atom transfer from BAC to create a cyanide ligand along with the alkyne $^i$Pr$_2$N–C≡C–N$^i$Pr$_2$. The iron complex is in equilibrium with an N$_2$-free species. Further reaction with CO leads to formation of a CO analogue, which can be independently prepared using NaCN as the cyanide source, while reaction with B(C$_6$F$_5$)$_3$ provides the cyanoborane derivative. | |
dc.description.version | postprint | |
dc.identifier.citation | Martinez, Jorge L., et al. "Cyanide Ligand Assembly by Carbon Atom Transfer to an Iron Nitride." J. Am. Chem. Soc., vol. 139, no. 40, 2017-9-21, https://doi.org/10.1021/jacs.7b08704. | |
dc.identifier.issn | 1520-5126 | |
dc.identifier.other | BRITE 1322 | |
dc.identifier.uri | https://hdl.handle.net/2022/33028 | |
dc.language.iso | en | |
dc.relation.isversionof | https://doi.org/10.1021/jacs.7b08704 | |
dc.relation.journal | J. Am. Chem. Soc. | |
dc.title | Cyanide Ligand Assembly by Carbon Atom Transfer to an Iron Nitride |
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