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                                       Details for article 12 of 72 found articles
 
 
  Different coordination modes of tetradentate Schiff bases in monomeric and dimeric oxorhenium(V) complexes
 
 
Title: Different coordination modes of tetradentate Schiff bases in monomeric and dimeric oxorhenium(V) complexes
Author: Gerber, Thomas I. A.
Luzipo, Dibanisile
Mayer, Peter
Appeared in: Journal of coordination chemistry
Paging: Volume 58 (2005) nr. 16 pages 1505-1512
Year: 2005-11-10
Contents: The reactions of the tetradentate amine-phenol type Schiff bases H2sal2en (1,2-ethylenebis(salicylideneimine) and H2sal2mp (1,2-benzylenebis(salicylideneimine)) with trans-[ReOCl3(PPh3)2] or (n-Bu4N)[ReOCl4] in air gave the products (µ-O)[ReO(sal2en)]2 (1) and [ReOCl(sal2mp)] (2), respectively. X-ray and spectroscopic studies have shown that 1 contains the linear O=Re-O-Re=O grouping, with the four donor atoms of sal2en2- coordinating in the square plane cis to the oxo ions. In 2, a cis oxo-chloro arrangement is observed with a phenolic oxygen being coordinated trans to the oxo group. The terminal Re=O bond lengths in 1 and 2 are 1.709(4) and 1.683(3) Å, respectively.
Publisher: Taylor & Francis
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 12 of 72 found articles
 
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