Charge separation in 9,9?-dianthryl and a special pair treated by a semi-empirical reaction field method

1990 ◽  
Vol 38 (S17) ◽  
pp. 189-206 ◽  
Author(s):  
S. Larsson ◽  
B. K�llbring
1988 ◽  
Vol 89 (5) ◽  
pp. 3086-3095 ◽  
Author(s):  
Kurt V. Mikkelsen ◽  
Hans Ågren ◽  
Hans Jo/rgen Aa. Jensen ◽  
Trygve Helgaker

2010 ◽  
Vol 111 (4) ◽  
pp. 904-913 ◽  
Author(s):  
Kristian O. Sylvester-Hvid ◽  
Kurt V. Mikkelsen ◽  
Mark A. Ratner

2001 ◽  
Vol 105 (14) ◽  
pp. 3583-3590 ◽  
Author(s):  
Robert W. J. Zijlstra ◽  
Ferdinand C. Grozema ◽  
Marcel Swart ◽  
Ben L. Feringa ◽  
Piet Th. van Duijnen

1968 ◽  
Vol 21 (2) ◽  
pp. 419 ◽  
Author(s):  
A Fulton ◽  
LE Lyons

The spectra of 20 purines and pyrimidines with chloranil, bromanil, and p-benzoquinone in dimethyl sulphoxide were studied. Most of the systems exhibited absorption bands which were concluded to be charge transfer in nature. The ionization energies of the molecules, derived from the positions of the bands, correlated well with the highest occupied molecular orbital energies calculated using the simple H�ckel method and were also in good agreement with ionization energy values calculated by a semi-empirical self-consistent field method.


2020 ◽  
Vol 73 (8) ◽  
pp. 669 ◽  
Author(s):  
Jeremy Hall ◽  
Rafael Picorel ◽  
Nicholas Cox ◽  
Robin Purchase ◽  
Elmars Krausz

We apply the differential optical spectroscopy techniques of circular polarisation of luminescence (CPL) and magnetic CPL (MCPL) to the study of isolated reaction centres (RCs) of photosystem II (PS II). The data and subsequent analysis provide insights into aspects of the RC chromophore site energies, exciton couplings, and heterogeneities. CPL measurements are able to identify weak luminescence associated with the unbound chlorophyll-a (Chl-a) present in the sample. The overall sign and magnitude of the CPL observed relates well to the circular dichroism (CD) of the sample. Both CD and CPL are reasonably consistent with modelling of the RC exciton structure. The MCPL observed for the free Chl-a luminescence component in the RC samples is also easily understandable, but the MCPL seen near 680nm at 1.8K is anomalous, appearing to have a narrow, strongly negative component. A negative sign is inconsistent with MCPL of (exciton coupled) Qy states of either Chl-a or pheophytin-a (Pheo-a). We propose that this anomaly may arise as a result of the luminescence from a transient excited state species created following photo-induced charge separation within the RC. A comparison of CD spectra and modelling of RC preparations having a different number of pigments suggests that the non-conservative nature of the CD spectra observed is associated with the ‘special pair’ pigments PD1 and PD2.


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