TY - JOUR
T1 - Alkyl chain elongation and acyl group effects in a series of Eu/Tb complexes with hexadentate π-electronic skeletons and their enhanced luminescence in solutions
AU - Ogata, Shuhei
AU - Goto, Naoto
AU - Sakurai, Shoya
AU - Ishii, Ayumi
AU - Hatanaka, Miho
AU - Yoshihara, Koushi
AU - Tanabe, Ryota
AU - Kayano, Kyosuke
AU - Magaribuchi, Ryo
AU - Goto, Kenta
AU - Hasegawa, Miki
N1 - Funding Information:
The authors acknowledge Prof. Makoto Handa and Prof. Michiko Egawa (Shimane University) for their kind discussions. This work was partly supported by grants-in-aid from Scientific Research on Innovative Areas of "Soft Crystals (area number: 2903)" (no. 17H06374; MH), MEXT Supported Program for the Strategic Research Foundation at Private Universities (2013-2017; MH), Network Joint Research Centre for Materials and Devices (2017; MH) and a SOKEN Project provided by Aoyama Gakuin University Research Institute (2016-2017; MH). MH also acknowledges Izumi Science and Technology Foundation for their financial support. SO thanks the Early Eagle Program for a subsidy from Aoyama Gakuin University. AI and Miho Hatanaka acknowledge the support of JST PRESTO.
Funding Information:
The authors acknowledge Prof. Makoto Handa and Prof. Michiko Egawa (Shimane University) for their kind discussions. This work was partly supported by grants-in-aid from Scientific Research on Innovative Areas of “Soft Crystals (area number: 2903)” (no. 17H06374; MH), MEXT Supported Program for the Strategic Research Foundation at Private Universities (2013–2017; MH), Network Joint Research Centre for Materials and Devices (2017; MH) and a SOKEN Project provided by Aoyama Gakuin University Research Institute (2016–2017; MH). MH also acknowledges Izumi Science and Technology Foundation for their financial support. SO thanks the Early Eagle Program for a subsidy from Aoyama Gakuin University. AI and Miho Hatanaka acknowledge the support of JST PRESTO.
Publisher Copyright:
© 2018 The Royal Society of Chemistry.
PY - 2018
Y1 - 2018
N2 - Five Eu complexes with long alkyl chain groups, abbreviated as EuLCx ("x" indicates the number of methylene groups: x = 8, 12, 14, 18, and 22), were synthesized to evaluate their structural and luminescence properties in chloroform. The mother helicate Eu complex, EuL, which has two bipyridine moieties bridged by an ethylenediamine, has been previously reported. A reduced form in which the azomethine groups of L also coordinated to the Eu ion, EuLH, was newly prepared. EuLH also adopts a helicate molecular structure based on single crystal X-ray structural analysis. The amine hydrogens of the bridging ethylenediamine of LH are active sites for substitution and were exchanged with five different alkyl chains to form EuLCx. Luminescence band positions and shapes of EuLCx in chloroform were completely identical, with a quantum yield of 37.1 ± 1.2 and a lifetime of around 1.25 ms. This indicates that the environments surrounding the Eu ion in the various complexes are all similar. Luminescence quantum yields of TbLH and TbLC18 are also strengthened, 48.7% in acetonitrile and 55% in chloroform, respectively. Potential energy surfaces were also described by using density functional theory, suggesting the possibility of a 1:2 complex of Eu and the ligand as a main luminescent species in solutions. This 1:2 complexation forms Eu-oxygen coordination using acyl groups. It indicates that the acyl group modification results in a different structure from the mother complexes.
AB - Five Eu complexes with long alkyl chain groups, abbreviated as EuLCx ("x" indicates the number of methylene groups: x = 8, 12, 14, 18, and 22), were synthesized to evaluate their structural and luminescence properties in chloroform. The mother helicate Eu complex, EuL, which has two bipyridine moieties bridged by an ethylenediamine, has been previously reported. A reduced form in which the azomethine groups of L also coordinated to the Eu ion, EuLH, was newly prepared. EuLH also adopts a helicate molecular structure based on single crystal X-ray structural analysis. The amine hydrogens of the bridging ethylenediamine of LH are active sites for substitution and were exchanged with five different alkyl chains to form EuLCx. Luminescence band positions and shapes of EuLCx in chloroform were completely identical, with a quantum yield of 37.1 ± 1.2 and a lifetime of around 1.25 ms. This indicates that the environments surrounding the Eu ion in the various complexes are all similar. Luminescence quantum yields of TbLH and TbLC18 are also strengthened, 48.7% in acetonitrile and 55% in chloroform, respectively. Potential energy surfaces were also described by using density functional theory, suggesting the possibility of a 1:2 complex of Eu and the ligand as a main luminescent species in solutions. This 1:2 complexation forms Eu-oxygen coordination using acyl groups. It indicates that the acyl group modification results in a different structure from the mother complexes.
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U2 - 10.1039/c7dt04899h
DO - 10.1039/c7dt04899h
M3 - Article
C2 - 29770370
AN - SCOPUS:85047720796
SN - 1477-9226
VL - 47
SP - 7135
EP - 7143
JO - Dalton Transactions
JF - Dalton Transactions
IS - 21
ER -