Orientation and Electronic Structure of the Primary Donor Radical Cation in Photosystem I:  A Single Crystals EPR and ENDOR Study

2001 ◽  
Vol 105 (6) ◽  
pp. 1225-1239 ◽  
Author(s):  
Hanno Käss ◽  
Petra Fromme ◽  
Horst T. Witt ◽  
Wolfgang Lubitz
2011 ◽  
Vol 53 (1) ◽  
pp. 41-47 ◽  
Author(s):  
A. T. Kozakov ◽  
K. A. Guglev ◽  
V. V. Ilyasov ◽  
I. V. Ershov ◽  
A. V. Nikol’skii ◽  
...  

1981 ◽  
Vol 82 ◽  
pp. 291-296 ◽  
Author(s):  
A SHELYKH ◽  
K SIDORIN ◽  
M KARIN ◽  
V BOBRIKOV ◽  
M KORSUKOVA ◽  
...  

1981 ◽  
Vol 103 (15) ◽  
pp. 4382-4388 ◽  
Author(s):  
K. W. Penfield ◽  
R. R. Gay ◽  
R. S. Himmelwright ◽  
N. C. Eickman ◽  
V. A. Norris ◽  
...  

2015 ◽  
Vol 17 (39) ◽  
pp. 25809-25821 ◽  
Author(s):  
Aude Bouchet ◽  
Johanna Klyne ◽  
Giovanni Piani ◽  
Otto Dopfer ◽  
Anne Zehnacker

The effects of ionisation and protonation on the geometric and electronic structure of a prototypical aromatic amino-alcohol with two chiral centres are revealed by IR and UV spectroscopy.


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


1994 ◽  
Vol 01 (04) ◽  
pp. 649-653 ◽  
Author(s):  
A.J. PATCHETT ◽  
S.S. DHESI ◽  
R.I.R. BLYTH ◽  
S.D. BARRETT

An intense photoemission feature is observed at a binding energy of ~10 eV in the UV photoemission spectra from the (0001) surfaces of bulk single crystals of rare-earth metals. This emission cannot be explained in terms of ground state electronic structure and we have been unable to attribute its existence to the presence of contamination of the surface. We present some evidence that may indicate its origin lies in the creation, by the photoemission process, of a metastable two-hole final state.


2016 ◽  
Vol 120 (38) ◽  
pp. 21710-21715 ◽  
Author(s):  
Takashi Komesu ◽  
Xin Huang ◽  
Tula R. Paudel ◽  
Yaroslav B. Losovyj ◽  
Xin Zhang ◽  
...  

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