Intramolecular energy transfer through charge transfer state in lanthanide compounds: A theoretical approach

2005 ◽  
Vol 122 (5) ◽  
pp. 054109 ◽  
Author(s):  
W. M. Faustino ◽  
O. L. Malta ◽  
G. F. de Sá
Keyword(s):  
Energy Transfer ◽  
Charge Transfer ◽  
Theoretical Approach ◽  
Charge Transfer State ◽  
Intramolecular Energy Transfer ◽  
Transfer State

The Role of the Ligand-to-Metal Charge-Transfer State in the Dipivaloylmethanate-Lanthanide Intramolecular Energy Transfer Process

2015 ◽  
Vol 2015 (18) ◽  
pp. 3019-3027 ◽  
Author(s):  
Yolanda C. Miranda ◽  
Leide L. A. L. Pereira ◽  
José H. P. Barbosa ◽  
Hermi F. Brito ◽  
Maria C. F. C. Felinto ◽  
...  
Keyword(s):  
Energy Transfer ◽  
Charge Transfer ◽  
Transfer Process ◽  
Energy Transfer Process ◽  
Charge Transfer State ◽  
Intramolecular Energy Transfer ◽  
Metal Charge ◽  
Metal Charge Transfer ◽  
Transfer State

scholarly journals Complete mapping of energy transfer pathways in the plant light-harvesting complex Lhca4

2020 ◽  
Vol 22 (44) ◽  
pp. 25720-25729
Author(s):  
Martijn Tros ◽  
Vladimir I. Novoderezhkin ◽  
Roberta Croce ◽  
Rienk van Grondelle ◽  
Elisabet Romero
Keyword(s):  
Energy Transfer ◽  
Charge Transfer ◽  
Light Harvesting ◽  
Electronic Spectroscopy ◽  
Low Energy ◽  
Charge Transfer State ◽  
Two Dimensional ◽  
Light Harvesting Complex ◽  
Complete Mapping ◽  
Transfer State

New insights on Lhca4 from two-dimensional electronic spectroscopy and modelling: population of the charge-transfer state and newly identified low-energy trap.

scholarly journals Directing energy transfer in Pt(bodipy)(mercaptopyrene) dyads

2019 ◽  
Vol 48 (31) ◽  
pp. 11690-11705 ◽  
Author(s):  
Peter Irmler ◽  
Franciska S. Gogesch ◽  
André Mang ◽  
Michael Bodensteiner ◽  
Christopher B. Larsen ◽  
...  
Keyword(s):  
Energy Transfer ◽  
Charge Transfer ◽  
Charge Transfer State ◽  
Transfer State

Pt(σ-bodipy)(mercaptopyrene) dyads offer separate emissions from the bodipy and the mercaptopyrene ππ* states and a pyrene-to-bodipy charge-transfer state. The energy ordering of these states can be manipulated by bodipy alkylation.

The Triplet State of Ketones in Solution: The Role of the Charge Transfer State in the Quenching of Triplet Acetone by Aromatic Molecules

1973 ◽  
Vol 51 (11) ◽  
pp. 1881-1884 ◽  
Author(s):  
R. O. Loutfy ◽  
R. W. Yip
Keyword(s):  
Energy Transfer ◽  
Charge Transfer ◽  
Energy Difference ◽  
Charge Transfer State ◽  
Triplet Energy ◽  
Excited Triplet ◽  
Aromatic Molecules ◽  
Triplet Energy Transfer ◽  
Transfer State

The rate constants for quenching of triplet acetone by a series of halobenzenes have been determined by flash emission technique. Quenching was found to be approximately a hundred times faster than that for triplet benzophenone. For both triplet ketones, quenching did not decrease with the increase in triplet energy difference between ketone and quencher (as expected for normal endothermic triplet energy transfer) and did not correlate with the i.p. of all of the quenchers studied. All of the qualitative features of the quenching results can be simply interpreted in terms of enhanced coupling of the locally excited triplet ketone and quencher states as a result of interaction with the charge transfer state.

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