Iron Carbonyl Thiocarbonyls: Effect of Substituting a Thiocarbonyl Group for a Carbonyl Group in Mononuclear and Binuclear Iron Carbonyl Derivatives

2009 ◽  
Vol 48 (5) ◽  
pp. 1974-1988 ◽  
Author(s):  
Zhong Zhang ◽  
Qian-shu Li ◽  
Yaoming Xie ◽  
R. Bruce King ◽  
Henry F. Schaefer
2013 ◽  
Vol 747 ◽  
pp. 106-112 ◽  
Author(s):  
Jianlin Chen ◽  
Shaoling Chen ◽  
Zhiguo Liu ◽  
Hao Feng ◽  
Yaoming Xie ◽  
...  

2013 ◽  
Vol 37 (3) ◽  
pp. 709-716 ◽  
Author(s):  
Huidong Li ◽  
Hao Feng ◽  
Weiguo Sun ◽  
Qunchao Fan ◽  
Yaoming Xie ◽  
...  

2014 ◽  
Vol 38 (9) ◽  
pp. 4282-4289 ◽  
Author(s):  
Zhong Zhang ◽  
Liang Pu ◽  
Qian-shu Li ◽  
R. Bruce King

The lowest energy Fe2(CO)n(CE)2 structures (E = S, Se, Te; n = 7, 6) do not have separate CE ligands but instead have coupled C2E2 ligands functioning as four to six-electron donors to the pair of iron atoms.


1960 ◽  
Vol 38 (12) ◽  
pp. 2508-2513 ◽  
Author(s):  
C. N. R. Rao ◽  
G. K. Goldman ◽  
A. Balasubramanian

The n → π* transition of the carbonyl group has been studied in solvents of varying degree of polarity and hydrogen-bonding ability, in a number of aliphatic carbonyl derivatives. Evidence for hyperconjugation of the alkyl groups in the electronically excited states of molecules has been presented.


2014 ◽  
Vol 166 ◽  
pp. 34-43 ◽  
Author(s):  
Guoliang Li ◽  
Lihua Liu ◽  
Jing Wang ◽  
Qian-shu Li ◽  
Yaoming Xie ◽  
...  

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