Optical spectra and excited state relaxation dynamics of Nd3+ in CaF2 single crystal

2011 ◽  
Vol 509 (36) ◽  
pp. 8880-8884 ◽  
Author(s):  
Qingguo Wang ◽  
Liangbi Su ◽  
Hongjun Li ◽  
Lihe Zheng ◽  
Xin Guo ◽  
...  
2011 ◽  
Vol 106 (1) ◽  
pp. 85-93 ◽  
Author(s):  
A. Strzęp ◽  
R. Lisiecki ◽  
P. Solarz ◽  
G. Dominiak-Dzik ◽  
W. Ryba-Romanowski ◽  
...  

2016 ◽  
Vol 18 (12) ◽  
pp. 8701-8709 ◽  
Author(s):  
Merle I. S. Röhr ◽  
Roland Mitrić ◽  
Jens Petersen

Even after laser excitation to high-lying bright states, diamantane fluoresces from the lowest excited state due to ultrafast nonadiabatic relaxation processes.


2018 ◽  
Vol 195 ◽  
pp. 159-165 ◽  
Author(s):  
Mirosław Karbowiak ◽  
Piotr Solarz ◽  
Radosław Lisiecki ◽  
Witold Ryba-Romanowski

2020 ◽  
pp. 117877
Author(s):  
Zixuan Fang ◽  
Hao Yu ◽  
Bo Zhang ◽  
Dapeng Jiang ◽  
Qinghui Wu ◽  
...  

2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Chunfan Yang ◽  
Qian Zhou ◽  
Zeqing Jiao ◽  
Hongmei Zhao ◽  
Chun-Hua Huang ◽  
...  

AbstractThe triplet metal to ligand charge transfer (3MLCT) luminescence of ruthenium (II) polypyridyl complexes offers attractive imaging properties, specifically towards the development of sensitive and structure-specific DNA probes. However, rapidly-deactivating dark state formation may compete with 3MLCT luminescence depending on different DNA structures. In this work, by combining femtosecond and nanosecond pump-probe spectroscopy, the 3MLCT relaxation dynamics of [Ru(phen)2(dppz)]2+ (phen = 1,10-phenanthroline, dppz = dipyridophenazine) in two iconic G-quadruplexes has been scrutinized. The binding modes of stacking of dppz ligand on the terminal G-quartet fully and partially are clearly identified based on the biexponential decay dynamics of the 3MLCT luminescence at 620 nm. Interestingly, the inhibited dark state channel in ds-DNA is open in G-quadruplex, featuring an ultrafast picosecond depopulation process from 3MLCT to a dark state. The dark state formation rates are found to be sensitive to the content of water molecules in local G-quadruplex structures, indicating different patterns of bound water. The unique excited state dynamics of [Ru(phen)2(dppz)]2+ in G-quadruplex is deciphered, providing mechanistic basis for the rational design of photoactive ruthenium metal complexes in biological applications.


2016 ◽  
Vol 656 ◽  
pp. 573-580 ◽  
Author(s):  
W. Ryba-Romanowski ◽  
J. Komar ◽  
T. Niedźwiedzki ◽  
M. Głowacki ◽  
M. Berkowski

2006 ◽  
Vol 28 (5) ◽  
pp. 551-555 ◽  
Author(s):  
A.S.S. de Camargo ◽  
M.R.B. Andreeta ◽  
A.C. Hernandes ◽  
L.A.O. Nunes

2015 ◽  
Vol 17 (47) ◽  
pp. 31978-31987 ◽  
Author(s):  
Franziska Buchner ◽  
Berit Heggen ◽  
Hans-Hermann Ritze ◽  
Walter Thiel ◽  
Andrea Lübcke

Time-resolved photoelectron spectroscopy is performed on aqueous guanosine solution to study its excited-state relaxation dynamics.


2005 ◽  
Vol 80 (4-5) ◽  
pp. 497-502 ◽  
Author(s):  
A. S. S. De Camargo ◽  
R. Almeida Silva ◽  
J. P. Andreeta ◽  
L. A. O. Nunes

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