CSIRO Publishing Books Journals About Us Shopping Cart You are here: Journals > Australian Journal of Chemistry   
Australian Journal of Chemistry
  An international journal for chemical science
 
Search
 
 
  Advanced Search
   

Journal Home
About the Journal
Editorial Board
Contacts
For Advertisers
Content
Online Early
Current Issue
Just Accepted
All Issues
Special Issues
Research Fronts
Sample Issue
Covers
For Authors
General Information
Notice to Authors
Submit Article
Open Access
For Referees
General Information
Review Article
For Subscribers
Subscription Prices
Customer Service
Print Publication Dates

 Early Alert
Subscribe to our Email Alert or RSS feeds for the latest journal papers.

 Connect with us
facebook   youtube

Affiliated with RACI

Royal Australian Chemical Institute
Royal Australian
Chemical Institute


 

Article << Previous     |     Next >>   Contents Vol 59(5)

Dinuclear Eu(iii), Gd(iii), and Tb(iii) Complexes of meso-1,2-Bis(ethylsulfinyl)ethane with 2,2′:6′,2′′-Terpyridine as Co-ligand

Jian-Rong Li A, Ruo-Hua Zhang A, Xian-He Bu A B

A Department of Chemistry, Nankai University, Tianjin 300071, China.
B Corresponding author. Email: buxh@nankai.edu.cn
 
PDF (292 KB) $25
 Export Citation
 Print
  


Abstract

Three dinuclear lanthanide complexes of flexible disulfoxide ligand meso-1,2-bis(ethylsulfinyl)ethane (L), [Ln2(L)2(μ-L)(tpy)4](ClO4)6(CHCl3)4 (Ln = Eu 1, Gd 2) and [Tb2(L)4(μ-L)(tpy)2](ClO4)6(CHCl3) 3 with 2,2′:6′,2′′-terpyridine (tpy) as co-ligand were synthesized and structurally characterized. In 1 and 2, the metal centre is nine-coordinated to two tpy and one-and-a-half L ligands, whereas in 3 it coordinates with one tpy and two-and-a-half L, which may be attributed to the influence of the lanthanide contraction. In such complexes the disulfoxide ligands perform two kinds of coordination modes, bridging and chelating, indicating their flexibility in the formation of such complexes.

   
Subscriber Login
Username:
Password:  

    


 
Top  Email this page
 
Legal & Privacy | Contact Us | Help

CSIRO

© CSIRO 1996-2012