Nine-Electron Donor Bridging Indenyl Ligands in Binuclear Iron Carbonyls

2012 ◽  
Vol 31 (14) ◽  
pp. 5005-5017 ◽  
Author(s):  
Rong Jin ◽  
Xiaohong Chen ◽  
Quan Du ◽  
Hao Feng ◽  
Yaoming Xie ◽  
...  
Keyword(s):  
Electron Donor ◽  
Iron Carbonyls ◽  
Binuclear Iron

Binuclear Iron Carbonyls and Their Significance as Catalytic Intermediates1

1957 ◽  
Vol 79 (23) ◽  
pp. 6116-6121 ◽  
Author(s):  
Heinz W. Sternberg ◽  
Raymond Markby ◽  
Irving Wender
Keyword(s):  
Iron Carbonyls ◽  
Binuclear Iron

Binuclear Cyclopentadienylcobalt Carbonyls:  Comparison with Binuclear Iron Carbonyls

2005 ◽  
Vol 127 (33) ◽  
pp. 11646-11651 ◽  
Author(s):  
Hongyan Wang ◽  
Yaoming Xie ◽  
R. Bruce King ◽  
Henry F. Schaefer
Keyword(s):  
Iron Carbonyls ◽  
Binuclear Iron

Halo- and carboxylato-bridged binuclear iron carbonyls

1979 ◽  
Vol 18 (10) ◽  
pp. 2926-2928 ◽  
Author(s):  
Graham N. Mott ◽  
Arthur J. Carty
Keyword(s):  
Iron Carbonyls ◽  
Binuclear Iron

Unsaturation in binuclear iron trifluorophosphine carbonyl derivatives: comparison with binary iron carbonyls

2012 ◽  
Vol 65 (14) ◽  
pp. 2459-2477 ◽  
Author(s):  
Shida Gong ◽  
Chaoyang Wang ◽  
Qian-Shu Li ◽  
Yaoming Xie ◽  
R. Bruce King
Keyword(s):  
Iron Carbonyls ◽  
Carbonyl Derivatives ◽  
Binuclear Iron

Determination of nickel and iron carbonyls in town gas

1963 ◽  
Vol 13 (12) ◽  
pp. 576-580
Author(s):  
A. B. Densham ◽  
P. A. A. Beale ◽  
R. Palmer
Keyword(s):  
Iron Carbonyls ◽  
Determination Of Nickel

Metal-Free Photoinduced Hydroalkylation Cascade Enabled by an Electron-Donor-Acceptor Complex

2020 ◽  
Author(s):  
José Tiago Menezes Correia ◽  
Gustavo Piva da Silva ◽  
Camila Menezes Kisukuri ◽  
Elias André ◽  
Bruno Pires ◽  
...  
Keyword(s):  
Electron Donor ◽  
Functional Group ◽  
Photoexcited Electron ◽  
One Pot ◽  
Quaternary Centers ◽  
Metal Free ◽  
Acceptor Complex ◽  
Catalyst Free ◽  
Donor Acceptor ◽  
Radical Cascade

A metal- and catalyst-free photoinduced radical cascade hydroalkylation of 1,7-enynes has been disclosed. The process is triggered by a SET event involving a photoexcited electron-donor-aceptor complex between NHPI ester and Hantzsch ester, which decomposes to afford a tertiary radical that is readily trapped by the enyne. <a>The method provides an operationally simple, robust and step-economical approach to the construction of diversely functionalized dihydroquinolinones bearing quaternary-centers. A sequential one-pot hydroalkylation-isomerization approach is also allowed giving access to a family of quinolinones. A wide substrate scope and high functional group tolerance was observed in both approaches</a>.

Three-Phase Electrochemistry of a Highly Lipophilic Neutral Ru-Complex Having a Tridentate Bis(benzimidazolate)pyridine Ligand

2020 ◽  
Author(s):  
Vishwanath R.S ◽  
Masa-aki Haga ◽  
Takumi Watanabe ◽  
Emilia Witkowska Nery ◽  
Martin Jönsson-Niedziolka
Keyword(s):  
Redox Potential ◽  
Organic Phase ◽  
Electron Donor ◽  
Ion Transfer ◽  
Neutral Complex ◽  
Pyridine Ligand ◽  
Electrochemical Testing ◽  
Ru Complex ◽  
Three Phase ◽  
Exceptional Stability

Here we describe the synthesis and electrochemical testing of a heteroleptic bis(tridentate) ruthenium(II) complex [Ru<sup>II</sup>(LR)(L)]<sup>0</sup> (LR =2,6-bis(1-(2-octyldodecan)benzimidazol-2-yl)pyridine, L = 2,6-bis(benzimidazolate)pyridine). It is a neutral complex which undergoes a quasireversible oxidation and reduction at relatively low potential. The newly synthetized compound was used for studies of ion-transfer at the three-phase junction because of the sensitivity of this method to cation expulsion. The [Ru<sup>II</sup>(LR)(L)]<sup>0</sup> shows exceptional stability during cycling and is sufficiently lipophilic even after oxidation to persist in the organic phase also using very hydrophilic anions such as Cl<sup>−</sup>. Given its low redox potential and strong lipophilicity this compound will be of interest as an electron donor in liquid-liquid electrochemistry.

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