The Iron−Sulfur Bond in Cytochromec

1999 ◽  
Vol 103 (33) ◽  
pp. 7031-7035 ◽  
Author(s):  
Carme Rovira ◽  
Paolo Carloni ◽  
Michele Parrinello
Keyword(s):  
2020 ◽  
Vol 11 (23) ◽  
pp. 6036-6044
Author(s):  
Maximilian Scheurer ◽  
Andreas Dreuw ◽  
Martin Head-Gordon ◽  
Tim Stauch

Using steered molecular dynamics simulations and strain analysis it is shown that, in contrast to previous assumptions, the experimentally found low rupture force of the iron–sulfur-bond in rubredoxin cannot be explained by hydrogen bond networks.


ChemInform ◽  
1987 ◽  
Vol 18 (11) ◽  
Author(s):  
L.-S. KAU ◽  
E. W. SVASTITS ◽  
J. H. DAWSON ◽  
K. O. HODGSON

1986 ◽  
Vol 25 (23) ◽  
pp. 4307-4309 ◽  
Author(s):  
Lung Shan Kau ◽  
Edmund W. Svastits ◽  
John H. Dawson ◽  
Keith O. Hodgson

1982 ◽  
Vol 104 (20) ◽  
pp. 5469-5472 ◽  
Author(s):  
P. M. Champion ◽  
B. R. Stallard ◽  
G. C. Wagner ◽  
I. C. Gunsalus

1987 ◽  
Vol 26 (12) ◽  
pp. 1978-1981 ◽  
Author(s):  
Norikazu Ueyama ◽  
Takashi Sugawara ◽  
Kazuyuki Tatsumi ◽  
Akira Nakamura

2019 ◽  
Author(s):  
Tristan Delcaillau ◽  
Alessandro Bismuto ◽  
Zhong Lian ◽  
Bill Morandi

A nickel-catalyzed carbon-sulfur bond metathesis has been developed to access high-value thioethers. 1,2-bis(dicyclohexylphosphino)ethane (dcype) is essential to promote this highly functional group tolerant reaction. Further, synthetically challenging macrocycles could be obtained in good yield in an unusual example of ring-closing metathesis which does not involve alkene bonds. In-depth organometallic studies support a reversible Ni(0)-Ni(II) pathway to product formation. Overall, this work does not only disclose a more sustainable and more functional group tolerant alternative to previous catalytic systems based on Pd, but also presents new applications and mechanistic information which are highly relevant to the further development and application of unusual single bond metathesis reactions.


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