An untethered: C 3v-symmetric triarylphosphine oxide locked by intermolecular hydrogen bonding

Timothy G. Carroll; Camden Hunt; Rachel Garwick; Guang Wu; Roman Dobrovetsky; Gabriel Ménard

doi:10.1039/c9cc01128e

An untethered: C _3v-symmetric triarylphosphine oxide locked by intermolecular hydrogen bonding

Timothy G. Carroll, Camden Hunt, Rachel Garwick, Guang Wu, Roman Dobrovetsky, Gabriel Ménard^*

^*Corresponding author for this work

School of Chemistry

University of California at Santa Barbara

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

Abstract

A para-substituted triphenylphosphine oxide with terminal vanadocene centers has been prepared and is, to our knowledge, the first example of an untethered C_3v-symmetric triarylphosphine oxide in the solid state. Crystallographic and DFT studies suggest this locked conformation is due to intermolecular H-bonding interactions. Electrochemical measurements suggest these interactions may persist in solution. A monometallic variant, adopting the standard C₃ propeller geometry, has also been synthesized for comparison.

Original language	English
Pages (from-to)	3761-3764
Number of pages	4
Journal	Chemical Communications
Volume	55
Issue number	26
DOIs	https://doi.org/10.1039/c9cc01128e
State	Published - 2019

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abstract = "A para-substituted triphenylphosphine oxide with terminal vanadocene centers has been prepared and is, to our knowledge, the first example of an untethered C3v-symmetric triarylphosphine oxide in the solid state. Crystallographic and DFT studies suggest this locked conformation is due to intermolecular H-bonding interactions. Electrochemical measurements suggest these interactions may persist in solution. A monometallic variant, adopting the standard C3 propeller geometry, has also been synthesized for comparison.",

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An untethered: C _3v-symmetric triarylphosphine oxide locked by intermolecular hydrogen bonding

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