158
Views
0
CrossRef citations to date
0
Altmetric
Original Articles

Synthesis, characterization, and styrene polymerization performance of organo yttrium complexes supported by imino-fuctionalized indenyl ligand

, &
Pages 1179-1185 | Received 23 Aug 2016, Accepted 16 Jan 2017, Published online: 23 Mar 2017
 

ABSTRACT

Amine elimination of Y[N(SiHMe2)2]3(THF)2 with the imino-functionalized indenyl ligand C9H7CH2CH = N-2,6-iPr2C6H3 in 1:1 and 1:2 molar ratio afforded the mono-indenyl-ligated yttrium bis(silylamide) complex (C9H6CH2CH = N-2,6-iPr2C6H3)Y[N(SiHMe2)2]2 (4) and the neutral yttrium complex (C9H6CH2CH = N-2,6-iPr2C6H3)(C9H6CH = CH-N-2,6-iPr2C6H3)Y (5), respectively. Both complexes were characterized by elemental analysis and NMR. X-ray single crystal structural diffraction showed that the central metal in 5 is four-coordinated by two indenyl ligands and two nitrogen atoms in η51-mode, if the indenyl ring is regarded as occupying an independent vertex. In the presence of AliBu3 and activated by one equimolar amount of [Ph3C][B(C6F5)4], complex 4 showed activity toward syndiospecific polymerization of styrene.

Acknowledgments

The authors are grateful to Mr. Zhang Yong at Suzhou University for X-ray single crystal analysis.

Funding

This project was supported by the National Natural Science Foundation of China (21572205) and Zhejiang Provincial Natural Science Foundation (LY15B020006).

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.