DPEphos

DPEphos
DPEphos structure
Names
Preferred IUPAC name
[Oxydi(2,1-phenylene)]bis(diphenylphosphane)
Other names
DPEphos, Bis[(2-diphenylphosphino)phenyl] ether
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.203.278 Edit this at Wikidata
EC Number
  • 678-206-0
  • InChI=1S/C36H28OP2/c1-5-17-29(18-6-1)38(30-19-7-2-8-20-30)35-27-15-13-25-33(35)37-34-26-14-16-28-36(34)39(31-21-9-3-10-22-31)32-23-11-4-12-24-32/h1-28H
    Key: RYXZOQOZERSHHQ-UHFFFAOYSA-N
  • C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3OC4=CC=CC=C4P(C5=CC=CC=C5)C6=CC=CC=C6
Properties
C36H28OP2
Molar mass 538.567 g·mol−1
Appearance white powder
Melting point 175–176 °C (347–349 °F; 448–449 K)
Hazards
GHS labelling:[1]
GHS07: Exclamation mark
Warning
H302, H315, H319, H335, H413
P261, P264, P264+P265, P270, P271, P273, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Bis[(2-diphenylphosphino)phenyl] ether, also known as DPEphos, is a wide bite angle diphosphine ligand used in inorganic and organometallic chemistry. The name DPEphos is derived from diphenyl ether (DPE) which makes up the ligand's backbone. It is similar to Xantphos, another diphosphine ligand, but is more flexible and has a smaller bite angle (104 vs 108°).[1] It is synthesized from chlorodiphenylphosphine and DPE.[2]

References

  1. ^ Birkholz (née Gensow), Mandy-Nicole; Freixa, Zoraida; van Leeuwen, Piet W. N. M. (2009). "Bite angle effects of diphosphines in C–C and C–X bond forming cross coupling reactions". Chemical Society Reviews. 38 (4): 1099–118. doi:10.1039/B806211K. PMID 19421583.
  2. ^ Kranenburg, Mirko; van der Burgt, Yuri E. M.; Kamer, Paul C. J.; van Leeuwen, Piet W. N. M.; Goubitz, Kees; Fraanje, Jan (June 1995). "New Diphosphine Ligands Based on Heterocyclic Aromatics Inducing Very High Regioselectivity in Rhodium-Catalyzed Hydroformylation: Effect of the Bite Angle" (PDF). Organometallics. 14 (6): 3081–3089. doi:10.1021/om00006a057.

Content Disclaimer

Informasi ini disarikan dari Wikipedia dan disajikan kembali untuk tujuan edukasi. Konten tersedia di bawah lisensi CC BY-SA 3.0. Kami tidak bertanggung jawab atas ketidakakuratan data yang bersumber dari kontribusi publik tersebut.

  1. The information displayed on this website is sourced in part or in whole from Wikipedia and has been adapted for the purpose of restating it. We strive to provide accurate and relevant information, however:
  2. There is no guarantee of absolute accuracy. Wikipedia is an open, collaborative project that can be edited by anyone, so information is subject to change.
  3. It is not intended to constitute professional advice. The content displayed is for informational and educational purposes only. For important decisions (e.g., medical, legal, or financial), please consult a professional.
  4. Content copyright. Wikipedia is licensed under the Creative Commons Attribution-ShareAlike License (CC BY-SA). This means that content may be reused with appropriate attribution and shared under a similar license.
  5. Responsible use. Any risk arising from the use of information from this website is entirely the responsibility of the user.