2,2'-Bis(2-indenyl) biphenyl

2,2′-Bis(2-indenyl) biphenyl
Names
	Preferred IUPAC name 2,2′-Di(1H-inden-2-yl)-1,1′-biphenyl
Identifiers
CAS Number	152952-99-3 ;
3D model (JSmol)	Interactive image;
ChemSpider	9318556 ;
PubChem CID	11143444;
CompTox Dashboard (EPA)	DTXSID20456782 ;
	InChI InChI=1S/C30H22/c1-2-10-22-18-25(17-21(22)9-1)27-13-5-7-15-29(27)30-16-8-6-14-28(30)26-19-23-11-3-4-12-24(23)20-26/h1-17,19H,18,20H2 Key: DGTWDUGCMACYFO-UHFFFAOYSA-N ; InChI=1/C30H22/c1-2-10-22-18-25(17-21(22)9-1)27-13-5-7-15-29(27)30-16-8-6-14-28(30)26-19-23-11-3-4-12-24(23)20-26/h1-17,19H,18,20H2 Key: DGTWDUGCMACYFO-UHFFFAOYAR;
	SMILES C1(C2=C(C3=CC(C=CC=C5)=C5C3)C=CC=C2)=C(C4=CC(C=CC=C6)=C6C4)C=CC=C1;
Properties
Chemical formula	C30H22
Molar mass	382.506 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

2,2′-Bis(2-indenyl) biphenyl is an organic compound with the formula [C₆H₄C₉H₇]₂. The compound is the precursor, upon deprotonation, to ansa-metallocene complexes within the area of transition metal indenyl complexes.

Metals studied with 2,2′-bis(2-indenyl) biphenyl include titanium, zirconium, and hafnium.^{[citation needed]} The ligand and its complexes have been prepared by the research group of the late Brice Bosnich at The University of Chicago.^[1] Zirconium and hafnium complexes made from this ligand were found to be active catalysts for the polymerization of the smallest alkenes – compounds with carbon-carbon double bonds—namely, ethylene and propylene.^{[citation needed]} The use of such complexes in the polymerization of alkenes has since been reported, and patented by DSM Research.^[2]^[3]

References edit

^ Ellis, W.W.; Hollis, T.K.; Odenkirk, W.; Whelan, J.; Ostrander, R.; Rheingold, A.L.; Bosnich, B. (1993). "Synthesis, Structure, and Properties of Chiral Titanium and Zirconium Complexes Bearing Biaryl Strapped Substituted Cyclopentadienyl Ligands". Organometallics. 12 (11): 4391–4401. doi:10.1021/om00035a026.
^ H. J. Arts, M. Kranenburg, R. H. A. M. Meijers, E. G. Ijpeij, G. J. M. Gruter and F. H. Beijer. Indenyl Compounds for the Polymerization of Olefins US Patent 6,342,622; Jan. 29, 2002.
^ E. G. Ijpeij; F. H. Beijer; H. J. Arts; C. Newton; J. G. de Vries; G. J. M. Gruter (2002). "A Suzuki Coupling Based Route to 2,2'-Bis#2-indenyl#biphenyl Derivatives" (PDF). J. Org. Chem. 67 (1): 169–176. doi:10.1021/jo016040i. PMID 11777455.

[1] Ellis, W.W.; Hollis, T.K.; Odenkirk, W.; Whelan, J.; Ostrander, R.; Rheingold, A.L.; Bosnich, B. (1993). "Synthesis, Structure, and Properties of Chiral Titanium and Zirconium Complexes Bearing Biaryl Strapped Substituted Cyclopentadienyl Ligands". Organometallics. 12 (11): 4391–4401. doi:10.1021/om00035a026.

[2] H. J. Arts, M. Kranenburg, R. H. A. M. Meijers, E. G. Ijpeij, G. J. M. Gruter and F. H. Beijer. Indenyl Compounds for the Polymerization of Olefins US Patent 6,342,622; Jan. 29, 2002.

[3] E. G. Ijpeij; F. H. Beijer; H. J. Arts; C. Newton; J. G. de Vries; G. J. M. Gruter (2002). "A Suzuki Coupling Based Route to 2,2'-Bis#2-indenyl#biphenyl Derivatives" (PDF). J. Org. Chem. 67 (1): 169–176. doi:10.1021/jo016040i. PMID 11777455.

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