scholarly journals Dph3 Enables Aerobic Diphthamide Biosynthesis by Donating One Iron Atom to Transform a [3Fe–4S] to a [4Fe–4S] Cluster in Dph1–Dph2

Author(s):  
Yugang Zhang ◽  
Dan Su ◽  
Boris Dzikovski ◽  
Sean H. Majer ◽  
Rachael Coleman ◽  
...  
Keyword(s):  
Nano Today ◽  
2021 ◽  
Vol 38 ◽  
pp. 101117
Author(s):  
Ruofan Li ◽  
Lan Ling ◽  
Wei-xian Zhang
Keyword(s):  

1986 ◽  
Vol 307 (2) ◽  
pp. C19-C22 ◽  
Author(s):  
Paul D. Beer ◽  
Stephen M. Charsley ◽  
Christopher J. Jones ◽  
Jon A. McCleverty
Keyword(s):  

Author(s):  
Nikolay G. Maksimov ◽  
Victor V. Verpekin ◽  
Dmitry V. Zimonin ◽  
Galina V. Burmakina ◽  
Oleg S. Chudin ◽  
...  

The chemical oxidation of the cluster CpReFePt(μ3-C=CHPh)(CO)5(dppe) (Cp = η5-C5H5, dppe = η2- Ph2P(CH2)2PPh2) resulted in a radical cation [CpReFePt(μ3-C=CHPh)(CO)5(dppe)]+• that is sufficiently stable only at low temperature. An electronic structure of the radical cation was studied by EPR and following parameters were obtained by comparison of the experimental and model spectrum: gx = 2.070 gy = 2.0295 gz = 1.997; Ax(31P) = 17 Ay(31P) = 49 Az(31P) = 35 (Gs);Ax(195Pt) = 62 Ay(195Pt) = 45 Az(195Pt) = 105 (Gs). An unpaired electron is seen to be mainly concentrated on the iron atom (85-90%) and partially on the platinum atom (10-15%). Further transformation of the radical cation led to the formation of the binuclear complex Cp(CO)2RePt(μ-C=CHPh)(dppe) and the Fe-carbonyl fragment


2014 ◽  
Vol 54 (3) ◽  
Author(s):  
V. Bėčytė ◽  
K. Mažeika ◽  
R. Juškėnas

Author(s):  
L. I. Kurkina ◽  
O. V. Farberovich ◽  
V. S. Stepanyuk ◽  
A. A. Katsnelson ◽  
A. Szasz

1995 ◽  
Vol 50 (8) ◽  
pp. 1222-1228 ◽  
Author(s):  
Hidenari Inoue ◽  
Hiromi Akahori ◽  
Yuri Ohno ◽  
Katsuo Nakazawa ◽  
Yoshimune Nonomura ◽  
...  

The adduct formation of iron(III) chlorophyll a with phosphines or phosphites has been studied by spectroscopic methods. The red-shift in the Soret and Q bands caused by the axial coordination of phosphine or phosphite to iron(III) chlorophyll a is an evidence for the autoreduction of the central iron(III) ion. The 31P{1H} NMR spectrum of bis-adducts measured in the presence of excess phosphine or phosphite ligands gave a single peak in the down field range compared to that of the corresponding free ligand. The ESR and X-ray photoelectron spectra have revealed that the central iron atom of the bis-adduct of iron chlorophyll a with phosphines or phosphites is divalent and in the low-spin state. The axial coordination of phosphine or phosphite influences the electronic configuration of the central iron atom and the macrocyclic chlorine ligand to induce the autoreduction of the central iron(III) ion.


1918 ◽  
Vol 85 (2193supp) ◽  
pp. 30-32
Author(s):  
Charles R. Sturdevant
Keyword(s):  

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