Synthesis and electrochemical characterization of bimetallic ruthenium complexes with the bridging eta2(s,s)-1,3-butadiyne-1,4-diyl ligand

The bis(ruthenium)alkyne complex [cis-{RuCl (bpy)2(mu-C<FONT FACE="Symbol">º</FONT>C-)}]2 (1) was obtained by treatment of 1 equiv of either 1,4-bis(trimethylsilyl)-1,3-butadiyne or bis(trimetylsilyl)acetylene with 2 equiv of cis-[RuCl2(bpy)2].2H2O, NaF and NaBF4 salts in metha...

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Bibliographic Details
Main Author: Stein,Edison (author)
Other Authors: Oki,Sergio Y. (author), Vichi,Eduardo J. S. (author)
Format: article
Language:eng
Published: 2000
Subjects:
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532000000300009
Country:Brazil
Oai:oai:scielo:S0103-50532000000300009
Description
Summary:The bis(ruthenium)alkyne complex [cis-{RuCl (bpy)2(mu-C<FONT FACE="Symbol">º</FONT>C-)}]2 (1) was obtained by treatment of 1 equiv of either 1,4-bis(trimethylsilyl)-1,3-butadiyne or bis(trimetylsilyl)acetylene with 2 equiv of cis-[RuCl2(bpy)2].2H2O, NaF and NaBF4 salts in methanol/CH2Cl2 mixture (10/1) in 52% and 35% yields, respectively. ¹H, 13C{H} NMR and principally electrochemical analyses confirmed that the same product was obtained from the two reactions. Cyclic voltammetric analyses of (1) from 0 to 1.20 V displays two one-electron quasi-reversible oxidation peaks attributed to the Ru(II)/Ru(III) couple. The redox processes are separated by 520 mV, indicating a significant electronic communication between the two metallic centers.