Dual Energy Transfer Pathways from an Antenna Ligand to Lanthanide Ion in Trivalent Europium Complexes with Phosphine-Oxide Bridges

2020 ◽  
Vol 124 (33) ◽  
pp. 6601-6606
Author(s):  
Shiori Miyazaki ◽  
Kiyoshi Miyata ◽  
Haruna Sakamoto ◽  
Fumiya Suzue ◽  
Yuichi Kitagawa ◽  
...  
2020 ◽  
Author(s):  
Shiori Miyazaki ◽  
Kiyoshi Miyata ◽  
Haruna Sakamoto ◽  
Fumiya Suzue ◽  
Yuichi Kitagawa ◽  
...  

<br>Trivalent europium (Eu3+) complexes are attractive materials for luminescence applications if energy transfer from antenna ligands to the lanthanide ion is efficient. However, the microscopic mechanisms of the transfer remain elusive and fundamental physical chemistry questions still require answers. We track the energy transfer processes in a luminescent complex Eu(hfa)3(DPPTO)2 (hfa: hexafluoroacetylacetonate, DPPTO: 2-diphenylphosphoryltriphenylene) using time-resolved photoluminescence spectroscopy. In addition to the conventional Dexter-type energy transfer pathway through the T1 state of the ligands, we discovered the Forster energy transfer pathway from the S1 of the DPPTO ligands to the 5D1 state of Eu3+ through the weak electronic interaction of a phosphine-oxide bridge. The short timescale of the energy transfer (16 ns, 127 ns) results in its high quantum yield. The coexistence of the distinct energy transfer pathways from a single chromophore is important for establishing design strategies of luminescent complexes. <br>


2020 ◽  
Author(s):  
Shiori Miyazaki ◽  
Kiyoshi Miyata ◽  
Haruna Sakamoto ◽  
Fumiya Suzue ◽  
Yuichi Kitagawa ◽  
...  

<br>Trivalent europium (Eu3+) complexes are attractive materials for luminescence applications if energy transfer from antenna ligands to the lanthanide ion is efficient. However, the microscopic mechanisms of the transfer remain elusive and fundamental physical chemistry questions still require answers. We track the energy transfer processes in a luminescent complex Eu(hfa)3(DPPTO)2 (hfa: hexafluoroacetylacetonate, DPPTO: 2-diphenylphosphoryltriphenylene) using time-resolved photoluminescence spectroscopy. In addition to the conventional Dexter-type energy transfer pathway through the T1 state of the ligands, we discovered the Forster energy transfer pathway from the S1 of the DPPTO ligands to the 5D1 state of Eu3+ through the weak electronic interaction of a phosphine-oxide bridge. The short timescale of the energy transfer (16 ns, 127 ns) results in its high quantum yield. The coexistence of the distinct energy transfer pathways from a single chromophore is important for establishing design strategies of luminescent complexes. <br>


Author(s):  
R. Marikumar ◽  
Rachna Devi ◽  
Sibani Mund ◽  
Kasturi Singh ◽  
Sivakumar Vaidyanathan

Two ancillary ligands were designed in the aspect of complete energy transfer to Eu(III) ion in the complex. Both the ligands were successfully synthesized and utilized for europium complexation (Eu(TTA)3-phen-fl-mCF3,...


2020 ◽  
Vol 92 (17) ◽  
pp. 11565-11572
Author(s):  
Yong Jian Jiang ◽  
Na Wang ◽  
Feng Cheng ◽  
Hua Rong Lin ◽  
Shu Jun Zhen ◽  
...  

2020 ◽  
Vol 8 (25) ◽  
pp. 8643-8653 ◽  
Author(s):  
Rachna Devi ◽  
Kasturi Singh ◽  
Sivakumar Vaidyanathan

Due to their structural flexibility and easy solution process capability, single-component white light-emitting pure organo-lanthanide complexes have been considered as promising candidates for solid-state lighting.


2017 ◽  
Vol 19 (11) ◽  
pp. 7728-7732 ◽  
Author(s):  
Huimin Zhao ◽  
Lixin Zang ◽  
Chengshan Guo

Energy transfer between the 4f energy levels of lanthanide ions and HMME determines whether lanthanide porphyrins can exhibit RTP.


Sign in / Sign up

Export Citation Format

Share Document