Electrochemical Behavior of Phosphine-Substituted Ruthenium(II) Polypyridine Complexes with a Single Labile Ligand
收藏NIAID Data Ecosystem2026-03-08 收录
下载链接：
https://figshare.com/articles/dataset/Electrochemical_Behavior_of_Phosphine_Substituted_Ruthenium_II_Polypyridine_Complexes_with_a_Single_Labile_Ligand/2272429
下载链接
链接失效反馈官方服务：
资源简介：
A series of phosphine-substituted
ruthenium polypyridine complexes, cis(P,Cl)-[Ru(trpy)(Pqn)Cl]PF6 (cis-Cl), trans(P,MeCN)-[Ru(trpy)(Pqn)(MeCN)](PF6)2 (trans-PN), cis(P,MeCN)-[Ru(trpy)(Pqn)(MeCN)](PF6)2 (cis-PN), and [Ru(trpy)(dppbz)(MeCN)](PF6)2 (PP), were synthesized and crystallographically
characterized (trpy = 2,2′:6′,2″-terpyridine,
Pqn = 8-(diphenylphosphanyl)quinoline, and dppbz = 1,2-bis(diphenylphosphanyl)benzene).
In electrochemical measurements for cis-PN and PP, the reduction of cis-PN resulted in the formation of trans-PN via cis–trans isomerization and that of PP proceeded via a two-electron-transfer reaction. The mechanism of
the electrochemical behaviors is discussed through consideration of
five-coordinated species, [Ru(trpy)(Pqn)]n+ or [Ru(trpy)(dppbz)]n+ (n = 0–2), formed by liberation of a monodentate labile ligand.
创建时间：
2016-02-17
