2,6-Bis(benzimidazol-2-yl)pyridines as more electron-rich and sterically accessible alternatives to 2,6-bis(imino)pyridine for group 13 coordination chemistry-Reference-Cited by-同舟云学术

2,6-Bis(benzimidazol-2-yl)pyridines as more electron-rich and sterically accessible alternatives to 2,6-bis(imino)pyridine for group 13 coordination chemistry

Published:2019 Issue:4 Volume:48 Page:1284-1291
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Swidan Ala'aeddeen¹²³⁴^ORCID,Binder Justin F.¹²³⁴^ORCID,Onge Blake J. St.¹²³⁴,Suter Riccardo⁵⁶⁷⁴^ORCID,Burford Neil⁵⁶⁷⁴^ORCID,Macdonald Charles L. B.¹²³⁴⁵^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry

2. University of Windsor

3. Windsor

4. Canada

5. Department of Chemistry

6. University of Victoria

7. Victoria

Abstract

2,6-bis(benzimidazol-2-yl)pyridines are more electron-rich yet more sterically open ligands for monovalent and trivalent group 13 elements than bis(imino)pyridines.

Funder

Natural Sciences and Engineering Research Council of Canada

Canada Foundation for Innovation

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/DT/C8DT04276D

Reference53 articles.

1. Key factors in pincer ligand design

2. Advances in Non-Metallocene Olefin Polymerization Catalysis