Abstract

in the title compound, C16H15N2 +·PF6 −, a precursor of N-heterocyclic carbene, the phenyl and benzyl rings are twisted away from the central imidazolium ring system, making dihedral angles of 70.30 (8) and 32.03 (10)°, respectively. The crystal structure is stabilized by C—H⋯F hydrogen bonds. Furthermore, P—F⋯π inter­actions involving imidazolium rings are observed [F⋯π = 2.9857 (16), P⋯π = 4.1630 (16) Å, P—F⋯π = 127.92 (6)°].

Highlights

  • In the title compound, C16H15N2+ÁPF6À, a precursor of Nheterocyclic carbene, the phenyl and benzyl rings are twisted away from the central imidazolium ring system, making dihedral angles of 70.30 (8) and 32.03 (10), respectively

  • The crystal structure is stabilized by C—HÁ Á ÁF hydrogen bonds

  • Related literature The first stable N-heterocyclic carbene was isolated by Arduengo et al (1991)

Read more

Summary

Ping Jiang

Key indicators: single-crystal X-ray study; T = 93 K; mean (C–C) = 0.003 A; R factor = 0.035; wR factor = 0.084; data-to-parameter ratio = 12.8. In the title compound, C16H15N2+ÁPF6À, a precursor of Nheterocyclic carbene, the phenyl and benzyl rings are twisted away from the central imidazolium ring system, making dihedral angles of 70.30 (8) and 32.03 (10), respectively. The crystal structure is stabilized by C—HÁ Á ÁF hydrogen bonds. Related literature The first stable N-heterocyclic carbene was isolated by Arduengo et al (1991). See: Wan et al (2008). See: Newman et al (2007); Herrmann (2002); Yang et al (2009)

Data collection
DÁ Á ÁA
Rigaku SPIDER diffractometer
Special details

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.